The Recall Desk

Archive

October 2022 recalls

446 recalls were announced in October 2022.

What the numbers show

Critical
9
Severe
95
High
273
Moderate
64
Low
5

Of the 446 recalls this month scored against our rubric, 2% are Critical, 21% are Severe.

1–100 of 446

  • SevereNHTSA·22V813000·2022-10-31

    Forest River Recalls Fifth Wheels Due to Holding Tank Retention Defect

    Forest River is recalling specific 2019-2022 fifth wheels because a cross-member may fail to retain holding tanks, increasing crash risk.

    Product
    COACHMEN — COACHMEN, SHASTA CHAPARRAL, PHOENIX, BROOKSTONE, CHAPARRAL LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V816000·2022-10-31

    2021 Hyundai Santa Fe Hybrid seat belt pretensioners may explode in crash

    Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.

    Product
    GENESIS — GENESIS, HYUNDAI G80 ELECTRIFIED, SANTA FE HYBRID, SANTA FE PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V814000·2022-10-31

    Tiffin Motorhomes Recall Multiple 2022-2023 Models for LPG Hose Leak Fire Risk

    Tiffin is recalling approximately 295 motorhomes from 2022-2023 because the LPG hose fitting connected to the regulator may leak at the swivel joint, creating a fire hazard in the presence of an ignition source.

    Product
    TIFFIN — TIFFIN ALLEGRO BREEZE, PHAETON, ALLEGRO, ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V815000·2022-10-31

    Volkswagen and Audi Vehicles Recalled for Tire Pressure Monitoring System Failure

    Volkswagen Group of America is recalling 296,044 Volkswagen and Audi vehicles (model years 2019-2021) because the tire pressure monitoring system may fail to detect simultaneous pressure loss in all four tires, increasing crash risk. Dealers will update the TPMS software at no charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI ATLAS CROSS SPORT, Q3, GOLF SPORTWAGEN, A3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·040-2022·2022-10-29

    Foster Farms Recalls Frozen Chicken Patties Due to Plastic Contamination

    Foster Farms is recalling approximately 148,000 pounds of frozen chicken patties sold at Costco in five states due to possible hard plastic contamination.

    Product
    Case Farms, Processing — Foster Farms Recalls Fully Cooked Frozen Chicken Patty Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·22V811000·2022-10-28

    Micro Bird Recalls G5 School Buses Due to Power Steering Defect

    Micro Bird is recalling 2019-2022 G5 school buses because a faulty connection may cause sudden loss of power steering and brake assist, increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·039-2022·2022-10-28

    JYC Enterprise Recalls Chicken and Pork Potstickers Produced Without Inspection

    JYC Enterprise is recalling approximately 33,280 pounds of frozen chicken and pork potstickers because they were repackaged and distributed without federal inspection.

    Product
    JYC Enterprise, Inc. — JYC Enterprise, Inc. Recalls Chicken and Pork Potsticker Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V812000·2022-10-28

    Micro Bird Recalls One 2019 G5 Transit Bus for Brake Fluid Leak

    Micro Bird is recalling one 2019 G5 transit bus because a faulty connection may cause power steering fluid loss, reducing brake assist and increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22T020000·2022-10-28

    Yokohama Recalls Tires with Incorrect Date Codes on Sidewalls

    Yokohama Off-Highway Tires America is recalling specific tires because the date code on the sidewall is incorrect, which hinders age identification.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23027·2022-10-27

    Goalsetter Wall-Mounted Basketball Goals Recall Due to Detachment Hazard

    Goalsetter is recalling about 18,000 wall-mounted basketball goals because they can detach from walls and fall. One fatality and multiple injuries have been reported.

    Product
    Goalsetter wall-mounted basketball goals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·038-2022·2022-10-27

    Lone Star Bakery Recalls Beef Shepherd's Pie Due to Copper Wire Contamination

    Lone Star Bakery is recalling beef shepherd's pie products that may contain copper wire pieces. No injuries have been reported, but consumers should not eat the product.

    Product
    Lone Star Bakery, Inc. — Lone Star Bakery, Inc. Recalls Beef Shepherd’s Pie Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    4 states
  • SevereCPSC·23026·2022-10-27

    Horizon T101-05 Treadmills Recalled for Unexpected Speed and Stop Hazard

    Horizon T101-05 folding treadmills can unexpectedly accelerate, change speed, or stop without user input, posing a fall hazard. About 192,000 units sold in the U.S. are affected; 71 injuries including broken bones have been reported.

    Product
    Horizon T101-05 Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V810000·2022-10-27

    Hyundai Recalls 2018 Santa Fe Sport Vehicles Due to Fire Risk

    Hyundai is recalling 44,396 2018 Santa Fe Sport vehicles because a faulty ABS module could cause an electrical short and engine compartment fire.

    Product
    HYUNDAI — HYUNDAI SANTA FE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23705·2022-10-27

    LG Energy Solution RESU 10H Batteries Recalled for Fire Hazard

    LG Energy Solution is recalling about 11,500 RESU 10H lithium-ion residential energy storage batteries because they can overheat and pose a fire risk with harmful smoke emissions. One incident of smoking and fire with property damage has been reported.

    Product
    LG Energy Solution "RESU 10H" Lithium-Ion Residential Energy Storage System Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23706·2022-10-27

    Punisher Adult Cycling Helmets Recalled Due to Head Injury Risk

    Bike USA is recalling about 3,400 Punisher Adult Cycling Helmets sold online from July 2020 through December 2021. The helmets do not meet safety standards for impact protection and can fail to protect the wearer in a crash.

    Product
    Punisher Adult Cycling Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23025·2022-10-27

    Tesla Cyberquad for Kids ATV Fails Federal Safety Standards

    Radio Flyer is recalling the Tesla Cyberquad for Kids (Model 914) because it violates federal safety standards for youth ATVs and lacks a required CPSC-approved action plan. One incident involving a tip-over has been reported.

    Product
    Tesla Cyberquad for Kids by Radio Flyer, Model Number 914
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23704·2022-10-27

    Amazon Basics Executive Desk Chairs Recalled for Fall and Injury Hazards

    Amazon is recalling about 11,400 Amazon Basics Executive Desk Chairs because the leg base can break, creating a fall and injury hazard. The company has received 13 reports of breaking leg bases, including one report of a minor shoulder injury.

    Product
    Amazon Basics Executive Desk Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V808000·2022-10-27

    2022 Chrysler 300 and Dodge vehicles TPMS sensor battery failure

    Chrysler and Dodge are recalling certain 2022 models because the tire pressure monitoring system sensor battery may fail prematurely, potentially increasing the risk of tire failure and crashes.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23024·2022-10-27

    Brother Recalls Meic Power Adapters for AirSure DF-2 Air Purifiers

    Brother is recalling Meic AC power adapters sold with AirSure DF-2 tabletop air purifiers because the adapter casing can break during plugging or unplugging, exposing metal prongs that pose electrical shock and electrocution hazards.

    Product
    Meic power adapters sold with Brother AirSure DF-2 Dynamic Filtration Tabletop Air Purifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0075-2023·2022-10-26

    Iso-Gard Filter S Medical Gas Filters Recalled Due to Device Splitting Risk

    TELEFLEX is recalling 355 units of Iso-Gard Filter S medical gas filters nationwide due to incidents of device splitting or detaching during use. The FDA classified this as a Class I recall.

    Product
    Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0074-2023·2022-10-26

    Medical Gas Filter Devices Recalled Due to Splitting and Detachment Risk

    Teleflex is recalling Iso-Gard Filter S microbial medical gas filters that may split or detach during use. The recall affects 164 units distributed nationwide.

    Product
    Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·037-2022·2022-10-26

    New Universal Nourishment Recalls Beef Burger Patties Produced Without Inspection

    New Universal Nourishment LLC is recalling approximately 368 pounds of raw, frozen beef burger patties that were repackaged and distributed without federal inspection.

    Product
    New Universal Nourishment LLC Recalls Beef Burger Patty Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0076-2023·2022-10-26

    Medical gas filter recalled due to splitting and detachment risk

    TELEFLEX LLC is recalling Iso-Gard Filter S medical gas filters due to incidents of device splitting or detaching during use. The affected filters may compromise patient safety.

    Product
    Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0073-2023·2022-10-26

    Iso-Gard Filter S Medical Gas Filter Recall Due to Splitting or Detachment

    TELEFLEX LLC is recalling Iso-Gard Filter S microbial medical gas filters due to incidents where the device may split or detach during use. The FDA classified this as a Class I recall.

    Product
    Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0072-2023·2022-10-26

    Iso-Gard Filter S Recalled for Device Splitting or Detachment During Use

    Teleflex is recalling Iso-Gard Filter S microbial filters (60,500 units) due to incidents of device splitting or detaching during use. The filters protect patients and equipment from bacterial and viral contamination in breathing systems.

    Product
    Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filters for use in breathing system for the protection of patient and equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0077-2023·2022-10-26

    Teleflex Catheter Mount and Filter May Split or Detach During Use

    Catheter mounts with filters (REF 191667-000100) used to connect endotracheal tubes or masks to breathing circuits may split or detach during patient use. Teleflex is recalling affected units distributed nationwide.

    Product
    Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube and mask)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0080-2023·2022-10-26

    Fenugreek dietary supplement recalled for potential Salmonella contamination

    Best Nutritionals LLC is recalling Best Naturals Fenugreek 610mg capsules due to potential Salmonella contamination. The product was distributed online via internet sellers and FBA.

    Product
    White plastic bottle with green, gold, and blue labeling containing 360, 610mg hard gelatin capsules of Fenugreek seed powder, labeled in part, "Best Naturals Fenugreek Premium Herbal 610mg 3rd Party Lab Tested 360 CAPSULES DIETARY SUPPLEMENT", best by 10/24, lot 102120
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0038-2023·2022-10-26

    Dark Chocolate Almonds recalled for undeclared milk allergen

    Dark Chocolate Almonds sold at Safeway, Albertsons, and Roths Fresh Market contain undeclared milk allergen. The FDA Class I recall affects 1,701 cases distributed in Oregon and Washington.

    Product
    Dark Chocolate Almonds distributed to Safeway/Albertsons is packaged in a clear clamshell container with a top label that displays PRODUCE Dark Chocolate Almonds , net weight of 9.5 oz., UPC 0 19061 19371 2. Distributed by Rivertrail Foods with an address of 4660 Ridge Dr. NE. S
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·22V805000·2022-10-26

    Sunset Park & RV Recalls 2022 Sun Lite and Rush Travel Trailers

    Sunset Park & RV is recalling 2022 Sun Lite and Rush travel trailers because a welded seam on the awning fabric may separate, causing the awning to drop unexpectedly.

    Product
    SUNSET PARK & RV — SUNSET PARK & RV SUNLITE, RUSH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0095-2023·2022-10-26

    BD Vacutainer Blood Alcohol Testing Tubes Recalled for Analytical Interference

    BD Vacutainer blood collection tubes are recalled due to isobutylene contamination that may cause false positive results in blood alcohol testing.

    Product
    BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0068-2023·2022-10-26

    Tastykake Glazed Caramel Apple Pie Recalled for Undeclared Soy

    Flowers Foods is recalling Tastykake Glazed Caramel Apple Pie because some packages contain undeclared soy lecithin, a major food allergen. Consumers with soy allergies should not consume this product.

    Product
    TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 08618 6 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0116-2023·2022-10-26

    Abbott MitraClip and TriClip Clip Delivery Systems: Locking Malfunction Risk

    Abbott is recalling MitraClip and TriClip Clip Delivery Systems due to clip locking malfunctions. Failed procedures may result in mitral regurgitation recurrence, device embolization, or tissue injury.

    Product
    Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR, MitraClip NTR Clip Delivery System CE/CDS0602-NTR, MitraClip XTR Clip Delivery System CE/CDS0602-XTR, MitraClip G4 Clip Delivery System NT CE/CDS0702-NT, MitraClip G4 Clip Delivery System NTW CE/CDS0702-NTW, Mi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0098-2023·2022-10-26

    Synthes Orthopedic Implant Drill Kit Recall: Incorrect Drill Guide Size

    Synthes (USA) Products LLC is recalling 81 SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kits nationwide due to incorrect drill guide sizing. The defect could result in bone damage and incorrectly placed drill holes during orthopedic surgery.

    Product
    SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No. SE-2020-10. Used with DePuy Synthes SPEEDSHIFT Continuous Compression Staple Implants for bone fixation and management of fracture and reconstructive surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2023·2022-10-26

    DePuy Synthes Hammertoe Implants Recalled for Incorrect Drill Guide Size

    Synthes (USA) Products LLC is recalling 196 DePuy Synthes Hammertoe Continuous Compression Implants due to an incorrect drill guide size that will not properly prepare bone for the implant, creating potential for bone damage.

    Product
    DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0067-2023·2022-10-26

    Tastykake Glazed Apple Pie Recalled for Undeclared Soy Allergen

    Flowers Foods is recalling Tastykake Glazed Apple Pie because soy lecithin is not declared on the labels. People with soy allergies could be at risk.

    Product
    TASTYKAKE GLAZED APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 00972 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0091-2023·2022-10-26

    IV Extension Sets Recalled for Bonded Joint Failure and Leakage Risk

    B. Braun extension sets (Product Code 470169) are recalled due to high probability of bonded joint failure, which may cause leakage or detachment during use, risking bloodstream infections and medication exposure.

    Product
    Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per carton. A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood upon insertion of a male luer connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0113-2023·2022-10-26

    Reusable Oral Syringe Recalled for Unapproved Plunger Material

    Medicina UK Ltd is recalling Reusable Oral Syringes because plungers were manufactured from unapproved polyethylene instead of the specified polypropylene material.

    Product
    Medicina Reusable Oral syringe 5ml Code: OTH05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0092-2023·2022-10-26

    IV extension set recall for potential joint failure and leakage risk

    B. Braun is recalling CARESITE SMALLBORE EXT SET T-PORT 5 IN. devices due to potential bonded joint failure that could cause leakage or detachment during use. The malfunction may result in delayed therapy, bloodstream infection risk, and exposure to hazardous medications.

    Product
    CARESITE SMALLBORE EXT SET T-PORT 5 IN., Product Code 470114, 100 units per carton. The A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0093-2023·2022-10-26

    Siemens N Antiserum to Human IgG Recall for High-Dose Performance Failure

    Siemens Healthcare Diagnostics recalls N Antiserum to Human IgG reagent for laboratory analyzers because it does not meet expected High-Dose Hook Effect performance specifications for IgG measurements in certain sample types.

    Product
    N Antiserum to Human IgG, 2mL Variant for BN II System and BN ProSpec System-IVD Siemens Material Number (SMN): 10446297
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0111-2023·2022-10-26

    Medicina Oral Tip Syringe recalled for unapproved plunger material

    Medicina Uk Ltd is recalling Medicina Oral Tip Syringe 2.5ml nationwide because the plunger component was manufactured with polyethylene instead of the approved polypropylene material.

    Product
    Medicina Oral Tip Syringe 2.5ml Code: OT25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2023·2022-10-26

    Dimension Vista HDLC Reagent Cartridge Recalled for Inaccurate Lab Results

    Siemens is recalling 1,592 units of Dimension Vista HDLC reagent cartridges due to potential for erroneous test results. Affected cartridges may produce falsely high or low HDL cholesterol measurements.

    Product
    Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent cartridge, IVD Siemens Material Number (SMN): 10464340 Catalog Number: K3048A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V806000·2022-10-26

    Multiple 2021-2022 Audi models recalled for rearview camera failure

    Volkswagen Group of America is recalling certain 2021-2022 Audi vehicles. The infotainment system may fail to display the rearview camera, reducing rear visibility and increasing crash risk.

    Product
    AUDI — AUDI S5 CABRIOLET, A3, Q8, Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V807000·2022-10-26

    Volkswagen Atlas and Cross Sport trailing arm bolt defect recall

    Volkswagen is recalling certain 2022 Atlas and 2022-2023 Cross Sport vehicles because driver-side rear trailing arm bolts may loosen and fall out, risking loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0107-2023·2022-10-26

    Medicina ENFit enteral syringe recall due to material specification defect

    Medicina is recalling ENFit 1ml enteral syringes because the plunger was manufactured with polyethylene instead of approved polypropylene. This material defect could affect plunger function and device safety.

    Product
    Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0013-2023·2022-10-26

    Acyclovir Sodium Injectable Recalled for Particulate Matter

    AuroMedics Pharma is recalling Acyclovir Sodium injection due to dark red, brown, and black particulate matter found in vials. Approximately 89,400 vials were distributed nationwide.

    Product
    ACYCLOVIR SODIUM — ACYCLOVIR SODIUM (ACYCLOVIR SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0112-2023·2022-10-26

    Medicina Reusable Oral Syringe Recalled for Unapproved Plunger Material

    Medicina Uk Ltd is recalling Medicina Reusable Oral syringes because the plunger was manufactured with polyethylene instead of the required polypropylene material. The 11,100 affected syringes do not meet raw material specifications.

    Product
    Medicina Reusable Oral syringe 1ml Code: OTH01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0096-2023·2022-10-26

    Laryngeal mask airway recalled for incorrect size marking

    Intersurgical Solus Standard size 3 laryngeal mask airways are marked with incorrect size 4 information, which may cause misuse or improper sizing of the airway device.

    Product
    Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0117-2023·2022-10-26

    MitraClip G4 and TriClip G4 Cardiac Devices Recalled for Clip Locking Malfunction

    Abbott has recalled MitraClip G4 and TriClip G4 cardiac repair devices due to clip locking malfunctions that may prevent proper device deployment. These malfunctions could lead to failed procedures and serious complications including device embolization.

    Product
    Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT, MitraClip G4 CDS NTW REPAIR-MR Clinical/CDS0704-NTW, MitraClip G4 CDS XT REPAIR-MR Clinical/CDS0704-XT, MitraClip G4 CDS XTW REPAIR-MR Clinical/CDS0704-XTW, TriClip NT Clip Delivery Sys CLIN/TCDS0203-NT, TriCli
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0115-2023·2022-10-26

    MitraClip Clip Delivery System Recalled for Locking Malfunctions

    Abbott Vascular is recalling MitraClip Clip Delivery System devices due to observed increases in clip locking malfunctions that can lead to recurrence of mitral regurgitation, device embolization, or tissue injury.

    Product
    Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT, MitraClip G4 Clip Delivery System NTW US/CDS0701-NTW, MitraClip G4 Clip Delivery System XT US/CDS0701-XT, MitraClip G4 Clip Delivery System XTW US/CDS0701-XTW.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0057-2023·2022-10-26

    Lyons Ready Care Thickened Sweet Tea Recalled for Product Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Sweet Tea with Lemon Nectar due to indication of product spoilage. Approximately 491 cases were distributed across all U.S. states.

    Product
    Lyons Ready Care Thickened Sweet Tea with Lemon Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Devices)·Z-0106-2023·2022-10-26

    Chest Tube Insertion Tray Recalled Due to Over-Sterilization of Suture Component

    Medline recalls CENTURION SnagFree Chest Tube insertion trays because a silk suture component was sterilized twice instead of once, potentially compromising its integrity. The affected lot contains 18 kits distributed in California and Texas.

    Product
    CENTURION SnagFree Chest Tube insertion Tray, Reorder CHT545
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0094-2023·2022-10-26

    N Antiserum to Human IgG Fails High-Dose Hook Effect Performance Standards

    Siemens N Antiserum to Human IgG reagent batches are not meeting performance standards for high-dose immunoassay testing. The issue affects 10,201 packs distributed nationwide and may result in inaccurate diagnostic test results.

    Product
    N Antiserum to Human IgG, 5mL Variant for BN II System and BN ProSpec System- IVD Siemens Material Number (SMN): 10446299
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0100-2023·2022-10-26

    Synthes SPEED implant recall: drill guide size mismatch in surgical kit

    Synthes is recalling SPEED 9X10X10mm surgical implant kits nationwide due to an incorrect-size drill guide that will not properly prepare bone for the implant, creating potential for bone damage.

    Product
    SPEED 9X10X10mm Continuous Compression Implant, Product No. SE-0910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0050-2023·2022-10-26

    Karlsburger Kitchens Turkey Gravy Mix Contains Undeclared Gluten

    Karlsburger Kitchens NSLP 140 Turkey Gravy Mix labeled as gluten-free contains undeclared gluten. The product was distributed in Kansas, Minnesota, Nebraska, and Wisconsin.

    Product
    Karlsburger Kitchens NSLP 140 Turkey Gravy Mix, Gluten Free. Packaged in the following sizes: 1. Item 32713. Net Weight 13 oz. (368 gm). 2. Item 32725. Net Weight 25 lb. (11.34 kg). Manufactured in a plant that handles Gluten. Karlsburger Foods, Inc., Monticello, MN
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0071-2023·2022-10-26

    Rocky Road Trail Mix recalled for glass contamination

    Diamond Foods' Rocky Road Trail Mix (20 oz bags) is being recalled due to glass pieces found in the product. Consumers should stop using affected batches immediately.

    Product
    Rocky Road Trail Mix, 20 oz UPC: 021130 162550 Store in refrigeration for freshness. Distributed by Better Living Brands, LLC, OP Box 99, Pleasanton, CA 94566
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0109-2023·2022-10-26

    Medicina Oral Tip Syringe Recall Due to Unapproved Plunger Material

    Medicina Uk Ltd is recalling 12,000 Oral Tip Syringes (Code: OT005) because the plunger component was manufactured with polyethylene instead of the approved polypropylene material. The syringes do not meet raw material specifications.

    Product
    Medicina Oral Tip Syringe 0.5ml Code: OT005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0097-2023·2022-10-26

    Medical Device Recall: Roche cobas 5800 False Results Due to Baseline Anomalies

    Roche Molecular Systems recalls the cobas 5800 PCR testing instrument due to false positive and invalid results caused by anomalous baselines. This may lead to erroneous or delayed diagnoses.

    Product
    cobas 5800 instrument, Material No. 08707464001. Used for automated Polymerase Chain Reaction (PCR) based Nucleic Acid Testing (NAT) in laboratory settings.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0015-2023·2022-10-26

    Saline Solution Injection Recalled Nationwide Due to Sterility and Leakage

    Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection distributed nationwide due to lack of assurance of sterility and potential leakage. Multiple lot numbers with expiration dates ranging from May 2023 to August 2023 are affected.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0099-2023·2022-10-26

    Surgical Implant Kit Recall: Incorrect Drill Guide Included

    Synthes surgical implant kits are being recalled because they contain an incorrect size drill guide that cannot properly prepare the bone for the implant, creating a risk of bone damage during surgery.

    Product
    SPEED 15X12X12mm Continuous Compression Implant, Product No. SE-1512
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0047-2023·2022-10-26

    Trader Joe's Organic Tortilla Chip Rounds recalled for undeclared milk and soy

    Trader Joe's Organic Yellow Tortilla Chip Rounds may contain undeclared milk and soy allergens. The product contains small amounts of Spicy Cheese Crunchies which were not listed on the label.

    Product
    16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-0449 Distributed and Sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and Sold Exclusively By: Trader Joe's, Monro
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0053-2023·2022-10-26

    Lyons Ready Care Thickened Orange Nectar Recalled for Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Nectar due to indication of product spoilage. The recall affects 1,272 cases distributed nationwide with specific lot numbers and best-by dates in March 2023.

    Product
    Lyons Ready Care Thickened Orange Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0062-2023·2022-10-26

    Lyons Ready Care Thickened Apple Juice Recalled for Spoilage Indication

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Juice due to indication of product spoilage. The recall affects 320 cases distributed nationwide.

    Product
    Lyons Ready Care Thickened Apple Juice packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Devices)·Z-0114-2023·2022-10-26

    Medicina Reusable Oral Syringe recalled for incorrect plunger material

    Medicina Uk Ltd is recalling Medicina Reusable Oral Syringe 2.5ml units because plunger components were manufactured with polyethylene instead of the specified polypropylene material.

    Product
    Medicina Reusable Oral syringe 2.5ml Code: OTH25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0110-2023·2022-10-26

    Oral Tip Syringes Recalled Due to Unapproved Plunger Material

    Medicina Oral Tip Syringes are being recalled because the plunger component was made with polyethylene instead of the approved polypropylene material. No illnesses or injuries have been reported.

    Product
    Medicina Oral Tip Syringe 1ml Code: OT01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2023·2022-10-26

    ULTRASITE US04TL Extension Sets recalled for bonded joint failure risk

    B. Braun is recalling ULTRASITE Extension Sets because the bonded joint has a high probability of failure during use. Device failure could cause leakage, bloodstream infections, and delays in therapy.

    Product
    ULTRASITE US04TL Smallbore T-Port Extension Set, Product Code 474515, 100 units per carton. to provide needle-free access on I.V. and Extension Sets
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0066-2023·2022-10-26

    Mrs. Freshley's Cherry Fruit Pie recalled for undeclared soy lecithin

    Flowers Foods is recalling Mrs. Freshley's Cherry Fruit Pie due to undeclared soy lecithin. Soy is a major allergen; consumers with soy allergies should not consume the product.

    Product
    Mrs. Freshley's Cherry Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 0081 0 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
    Category
    Food
    Distribution
    50 states
  • HighFDA (Food)·F-0044-2023·2022-10-26

    Cheese Straws Recalled for Undeclared Wheat and Milk Allergens

    Flathau's Fine Foods is recalling Cheese Straws Delta Bred products due to undeclared wheat and milk allergens. 433 units were distributed across 12 states. Consumers with allergies should stop consuming and discard affected products.

    Product
    Flathau's Fine Foods Cheese Straws Delta Bred Cheese Straws packaged in 4oz and 6oz cartons 12 packages per case
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0048-2023·2022-10-26

    Seeking Health Optimal Multivitamin Chewable Supplement Recalled for Excess Copper

    Seeking Health LLC is recalling Optimal Multivitamin Chewable Dietary Supplement tablets because lab testing found higher copper levels than stated on the label.

    Product
    Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 810007520902. Product labels read in part: Adults and children age 4 and over; Chew 2 tablets daily. Servi
    Category
    Consumer Product
    Distribution
    51 states
  • HighFDA (Food)·F-0065-2023·2022-10-26

    Mrs. Freshley's Apple Fruit Pie recalled for undeclared soy allergen

    Flowers Foods is recalling Mrs. Freshley's Apple Fruit Pie (4.5 oz) because some packages may contain undeclared soy lecithin, a major allergen. Consumers with soy allergies should not consume the affected product.

    Product
    Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
    Category
    Food
    Distribution
    50 states
  • HighNHTSA·22V804000·2022-10-26

    Rearview camera display malfunction in 2022 Lamborghini Urus vehicles

    The infotainment system in certain 2022 Lamborghini Urus vehicles may become damaged, causing the rearview camera display to become inoperative. This reduces rear visibility and increases the risk of a crash.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0104-2023·2022-10-26

    Lithium diagnostic assay may display falsely elevated results on Atellica CH analyzer

    The Atellica CH Lithium_2 diagnostic assay may produce falsely elevated lithium readings on the Atellica CH 930 analyzer, potentially leading to incorrect medication dosage adjustments. No illnesses have been reported.

    Product
    Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11532401. in vitro diagnostic assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0054-2023·2022-10-26

    Lyons Ready Care Thickened Apple Honey Nectar Recalled Due to Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Honey Nectar due to indications of product spoilage. The nationwide recall affects 645 cases with specific lot numbers and best-by dates in March 2023.

    Product
    Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0049-2023·2022-10-26

    Karlsburger Kitchens beef gravy mix recalled for undeclared gluten

    Karlsburger Kitchens beef gravy mix is recalled for containing undeclared gluten despite its gluten-free label. The product poses a risk to consumers with celiac disease or gluten sensitivity.

    Product
    Karlsburger Kitchens NSLP 140 Beef Gravy Mix, Gluten Free. Packaged in the following sizes: 1. Item 32312. Net Weight 12 oz (340 gm) 2. Item 32325. Net Weight 25 lb. (11.34 kg). Manufactured in a plant that handles Gluten. Karlsburger Foods, Inc Monticello, MN 55362.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0070-2023·2022-10-26

    Tastykake Glazed Lemon Pie Recalled for Undeclared Soy

    Flowers Foods recalled Tastykake Glazed Lemon Pies due to undeclared soy lecithin in certain packages. Products with Enjoy By dates of Oct. 28, 31, Nov. 4, and 7 are affected.

    Product
    TASTYKAKE GLAZED LEMON FLAVORED PIE NET WT 4.5 OZ (128g) UPC 0 25600 00967 3 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
    Category
    Food
    Distribution
    50 states
  • HighFDA (Food)·F-0040-2023·2022-10-26

    Turner's Peach Cottage Cheese Recalled for Bacterial Spoilage

    Titusville Dairy Products Co. is recalling Turner's Peach Whole Milk Cottage Cheese (5.3oz) distributed in Pennsylvania due to bacterial spoilage. Consumers should not consume the product and should discard it.

    Product
    Turner's Peach Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300167
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0069-2023·2022-10-26

    Tastykake Glazed Cherry Pie Recalled Due to Undeclared Soy Lecithin

    Flowers Foods is recalling Tastykake Glazed Cherry Pie due to undeclared soy lecithin in the product. The recalled product may pose a health risk to consumers with soy allergies.

    Product
    TASTYKAKE GLAZED CHERRY PIE NET WT 4.5 OZ (128g) UPC 0 25600 00969 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
    Category
    Food
    Distribution
    50 states
  • HighFDA (Food)·F-0064-2023·2022-10-26

    Nestle Cookie Dough Recalled for Plastic Contamination

    Nestle-USA is recalling Stuffed Chocolate Chip Cookie Dough due to consumer complaints of white plastic pieces found in the product. Consumers should not eat the product.

    Product
    "***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"
    Category
    Food
    Distribution
    40 states
  • HighFDA (Food)·F-0063-2023·2022-10-26

    Lyons Ready Care Thickened Orange Juice recalled for spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Juice 46 fl oz cartons due to indication of product spoilage. Specific lot numbers distributed nationwide are affected.

    Product
    Lyons Ready Care Thickened Orange Juice packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0039-2023·2022-10-26

    Turner's Whole Milk Cottage Cheese Recalled for Bacterial Spoilage

    Titusville Dairy Products Co. is recalling Turner's Whole Milk Cottage Cheese (5.3oz) due to bacterial spoilage. Approximately 4,270 units were distributed to Pennsylvania.

    Product
    Turner's Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300166
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0043-2023·2022-10-26

    Market Pantry White Fudge Animal Cookies Recalled for Metal Contamination

    Market Pantry White Fudge Animal Cookies sold at Target may contain metal fragments. D. F. Stauffer Biscuit Co is recalling 883 cases distributed nationwide.

    Product
    White frosted animal cookies with multi-colored non-pareils in a 44oz plastic jug labeled "Market Pantry White Fudge Animal Cookies"
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0011-2023·2022-10-26

    Rifampin Capsules recalled due to excessive impurity levels

    Golden State Medical Supply Inc. is recalling Rifampin Capsules, USP, 300 mg, because samples exceeded acceptable limits for 1-Methyl-4-Nitrosopoperazine (MNP), an impurity. Multiple lot numbers were distributed nationwide.

    Product
    Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bottle (NDC 51407-323-60), c) 100-count bottle (NDC 51407-323-01), Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0061-2023·2022-10-26

    Imperial Thickened Cranberry Cocktail Honey Recalled for Product Spoilage

    Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Honey due to indication of product spoilage. Consumers who have purchased affected cases should stop using the product.

    Product
    Imperial Thickened Cranberry Cocktail Honey packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Devices)·Z-0102-2023·2022-10-26

    ARROW Midline Catheter Kit Mislabeled with Wrong Device Type

    ARROW INTERNATIONAL Inc. is recalling an ARROW Pressure Injectable Arrowgard Blue Advance Midline Catheter Kit due to mislabeling. The package labels incorrectly specify a double-lumen 5.5 French catheter, but the kit contains a single-lumen 4.5 French catheter.

    Product
    ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1. For peripheral access to the venous system for intravenous therapy, blood sampling, infusion, and pressure injection of contrast media.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0046-2023·2022-10-26

    Nick's Krispi Nougat Protein Bar Recalled for Undeclared Hazelnut

    Nick's Krispi Nougat Protein Bar is being recalled because the product contains hazelnuts that are not declared on the label. This poses a risk to consumers with tree nut allergies.

    Product
    Nick's Krispi Nougat Protein Bar, 1.76 oz., in foil wrapper in 12 pack boxes. UPC: 00850009682345 Product of North Macedonia Distributed by LUB Foods USA, Inc. El Segundo, CA 90245
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0105-2023·2022-10-26

    Medical device assay may report falsely elevated lithium levels

    Siemens' Atellica CH Lithium diagnostic assay may falsely report elevated lithium levels, potentially leading to incorrect dose adjustments in patients on lithium therapy.

    Product
    Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0060-2023·2022-10-26

    Lyons Magnus Thickened Cranberry Cocktail Nectar Recalled for Product Spoilage

    Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Nectar due to indication of product spoilage. Approximately 2094 cases were distributed nationwide.

    Product
    Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0051-2023·2022-10-26

    Tuscan Garden Italian Dressing Recalled for Undeclared Soy and Wheat Allergens

    Tuscan Garden Restaurant Style Italian Dressing is being recalled due to undeclared soy and wheat allergens. The recall affects 26,370 mixed cases distributed across 20 states.

    Product
    Tuscan Garden Restaurant Style Italian Dressing , Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case containing 3 Dressing flavors, including 8 bottles of the Restaurant Style Italian
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-0103-2023·2022-10-26

    Optima Coil System Pouch Labels Do Not Match Carton Labels

    BALT USA is recalling Optima Coil System models OPTI0208CSS10 and OPTI0308CSS10 due to a labeling discrepancy where pouch labels do not match carton labels. These endovascular devices require verification before use.

    Product
    Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0108-2023·2022-10-26

    Medicina ENFit Enteral Syringes Recalled for Incorrect Plunger Material

    Medicina Uk Ltd is recalling Medicina ENFit 5ml Reusable Enteral Syringes because the plunger component was manufactured with polyethylene instead of the specified polypropylene material.

    Product
    Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0012-2023·2022-10-26

    Rifampin Capsules recalled due to excess nitrosamine impurity

    Golden State Medical Supply Inc. is recalling Rifampin Capsules, 150 mg, due to elevated levels of 1-Methyl-4-Nitrosopiperazine (MNP) exceeding the FDA interim specification limit of 5 ppm. Affected lots are distributed nationwide.

    Product
    Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0014-2023·2022-10-26

    OTC Sinus Pressure and Pain Cough Product Mislabeled as Decongestant-Free

    Walgreens Sinus Pressure, Pain & Cough tablets are mislabeled as 'Decongestant Free' but contain Phenylephrine HCl, a nasal decongestant. The labeling error affects 66,384 boxes distributed nationwide.

    Product
    SINUS PRESSURE, PAIN AND COUGH — SINUS PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2023·2022-10-26

    FDA Recalls Flunisolide Nasal Solution Due to Out-of-Specification Impurities

    Ingenus Pharmaceuticals is recalling Flunisolide Nasal Solution nationwide because the product contains impurities that exceed acceptable limits. The recall affects two lots distributed across the United States.

    Product
    FLUNISOLIDE — FLUNISOLIDE (FLUNISOLIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0055-2023·2022-10-26

    Lyons Ready Care Thickened Cranberry Nectar Recalled for Product Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Cranberry Nectar due to indication of product spoilage. Approximately 999 cases were distributed across all U.S. states.

    Product
    Lyons Ready Care Thickened Cranberry Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • ModerateFDA (Food)·F-0052-2023·2022-10-26

    Lyons Ready Care Thickened Apple Nectar Recalled for Product Spoilage

    Lyons Magnus LLC recalls Lyons Ready Care Thickened Apple Nectar in 46 fl oz cartons due to product spoilage. Affected products were distributed nationwide.

    Product
    Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • ModerateFDA (Food)·F-0042-2023·2022-10-26

    Turner's Cottage Cheese Recalled for Bacterial Spoilage

    Titusville Dairy Products Co. is recalling Turner's Apple Cinnamon Whole Milk Cottage Cheese (5.3oz) due to bacterial spoilage. The affected products were distributed to a direct consignee in Pennsylvania.

    Product
    Turner's Apple Cinnamon Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300169
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0056-2023·2022-10-26

    Lyons Ready Care Thickened Cranberry Honey Nectar Recalled for Product Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Cranberry Honey Nectar due to indication of product spoilage. The recall involves 468 cases distributed across 49 states.

    Product
    Lyons Ready Care Thickened Cranberry Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • ModerateFDA (Food)·F-0041-2023·2022-10-26

    Turner's Pineapple Cottage Cheese Recalled for Bacterial Spoilage

    Turner's Pineapple Whole Milk Cottage Cheese 5.3oz is being recalled due to potential bacterial spoilage. The product was distributed in Pennsylvania; affected consumers should discard it.

    Product
    Turner's Pineapple Whole Milk Cottage Cheese 5.3oz. (150g) UPC:3573300168
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0059-2023·2022-10-26

    Imperial Thickened Orange Nectar Recalled for Product Spoilage

    Lyons Magnus LLC is recalling Imperial Thickened Orange Nectar due to indication of product spoilage. The 46 fl oz cartons were distributed nationwide.

    Product
    Imperial Thickened Orange Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • ModerateFDA (Food)·F-0058-2023·2022-10-26

    Imperial Thickened Apple Honey Nectar Recalled for Spoilage Risk

    Lyons Magnus LLC is recalling Imperial Thickened Apple Honey Nectar in 46 fl oz cartons due to indication of product spoilage. The product was distributed nationally.

    Product
    Imperial Thickened Apple Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states

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