The Recall Desk

Archive

March 2021 recalls

387 recalls were announced in March 2021.

What the numbers show

Critical
11
Severe
150
High
165
Moderate
46
Low
15

Of the 387 recalls this month scored against our rubric, 3% are Critical, 39% are Severe.

Which agencies issued them

301–387 of 387

  • LowFDA (Food)·F-0336-2021·2021-03-10

    Ferrara Candy Company Recalls Assorted Candy Heart Box for Undeclared Ingredients

    Ferrara Candy Company is recalling assorted candy Heart Boxes containing Laffy Taffy, Nerds, and SweeTarts due to undeclared ingredients on the retail packaging.

    Product
    Ferrara Candy Company assorted candy Heart Box, including Laffy Taffy, Nerds, and SweeTarts candies. 10 retail units per wholesale case. Package UPC 0 41420 04965 1
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V150000·2021-03-09

    Autocar Recalls 2020 Legend Vehicles Due to Wiring Harness Defect

    Autocar is recalling 2020 Legend vehicles because a wiring harness may disconnect, causing loss of headlights and wipers. This increases the risk of a crash.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V149000·2021-03-09

    Autocar Recalls 2020-2021 Legend Vehicles for Steering Column Defect

    Autocar is recalling 2020-2021 Legend vehicles because the steering column tilt control cable may contact the steering shaft, potentially causing it to bind and increasing steering effort.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V148000·2021-03-09

    Shyft Group Recalls 2017-2019 Utilimaster Mobile Maintenance Trucks

    Shyft Group is recalling 2017-2019 Utilimaster Mobile Maintenance Trucks equipped with a generator set because a flexible exhaust tube may tear, releasing hot gases and increasing fire risk.

    Product
    UTILIMASTER — UTILIMASTER MOBILE MAINTENANCE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V147000·2021-03-09

    2020-2021 RAM ProMaster City ABS Module Defect Poses Braking Failure Risk

    Chrysler is recalling 2020-2021 RAM ProMaster City vehicles due to potential internal damage to the ABS module, which may cause loss of braking performance. Dealers will replace the module free of charge.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E017000·2021-03-08

    WP Dynamics Lift Kit Recall for Improperly Treated Bolts

    WP Dynamics is recalling ReadyLIFT Lift Kits for certain Ford and Dodge trucks because improperly heat-treated bolts may break, risking suspension separation and loss of vehicle control.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E016000·2021-03-08

    MEKRA Recalls Exterior Rearview Mirror Housings for Detachment Risk

    MEKRA Lang North America is recalling specific exterior rearview mirror housings because the glass may detach, reducing visibility or creating road hazards.

    Product
    VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V140000·2021-03-05

    Ford Recalls 2021 Mustang Mach-E for Loose Front Subframe Bolts

    Ford is recalling 2021 Mustang Mach-E vehicles because front subframe bolts may not have been tightened properly, which could reduce crash performance and increase injury risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V142000·2021-03-05

    Volkswagen Recalls 2018-2019 Atlas Vehicles Due to Tire Defect

    Volkswagen is recalling 2018-2019 Atlas vehicles equipped with specific Continental tires that may have been over-cured during production, posing a risk of sudden air loss or loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V143000·2021-03-05

    Custom Truck Recalls Two Vehicles for Excessively Bright LED Lights

    Custom Truck is recalling one 2016 Ford F-550 and one 2018 International 4000 because their LED lights are too bright, potentially blinding other drivers.

    Product
    CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550, INTERNATIONAL 4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V141000·2021-03-05

    2021 Forest River Cardinal and Wildcat furnace flue misalignment recall

    Forest River is recalling certain 2021 Cardinal and Wildcat recreational vehicles due to furnace flue misalignment. Furnace exhaust may leak into the living space, creating a risk of injury or death.

    Product
    FOREST RIVER — FOREST RIVER WILDCAT, CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V137000·2021-03-04

    KIA Sportage and Cadenza electrical short circuit poses engine fire risk

    Certain 2017-2021 Sportage and 2017-2019 Cadenza vehicles have a defective hydraulic control unit that may short-circuit and ignite an engine compartment fire. Owners should park outside until repairs are completed.

    Product
    KIA — KIA SPORTAGE, CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V138000·2021-03-04

    2020-2021 Nissan Altima tie rod fastener defect may cause steering loss

    Nissan is recalling certain 2020-2021 Altima vehicles because the tie rod ball joint fastener was not tightened properly. This could cause the fastener to detach and result in loss of steering control.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V134000·2021-03-04

    Ferrara Recalls 2019-2020 Inferno Vehicles for Steering Gear Bolt Issue

    Ferrara Fire Apparatus is recalling 2019-2020 Inferno vehicles because steering gear mounting bolts may loosen, causing steering difficulties and increased crash risk.

    Product
    FERRARA — FERRARA INFERNO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V139000·2021-03-04

    Nissan Recalls Infiniti FX35 and FX45 Vehicles for Air Bag Defect

    Nissan is recalling specific Infiniti FX35 and FX45 vehicles because a previously replaced front passenger air bag cushion was folded incorrectly, which could tear during deployment.

    Product
    INFINITI — INFINITI FX35, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21725·2021-03-04

    Casa Kids Recalls Cabina Bunk Beds for Fall Hazard

    Casa Kids is recalling Cabina Bunk Beds because loose screws can cause the mattress foundation to fall, posing a risk to children.

    Product
    Cabina Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21724·2021-03-04

    Polaris Recalls Ranger and ProXD Vehicles Due to Throttle Crash Hazard

    Polaris is recalling approximately 15,800 Ranger and ProXD off-road vehicles because the throttle pedal may stick or return slowly, creating a crash risk.

    Product
    Model Year 2020-2021 RANGER 1000, RANGER CREW 1000, RANGER XP 1000, and RANGER CREW XP 1000 and Model Year 2020 ProXD 2000G, ProXD 2000G H, ProXD 4000G, and ProXD 4000G H
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0286-2021·2021-03-03

    Cisatracurium Besylate Injection Recalled Due to Labeling Error

    Meitheal Pharmaceuticals is recalling 34,860 vials of Cisatracurium Besylate Injection because cartons were mislabeled as Phenylephrine Hydrochloride.

    Product
    CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0269-2021·2021-03-03

    NDAL Recalls ManukaGuard Nasal Spray Due to Yeast Contamination

    NDAL Mfg Inc. is recalling ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray because the product was confirmed to contain yeast.

    Product
    ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270 measured sprays, Distributed by Ndal Laboratories, 449 Alvarado St., Monterey, CA 93940 (bottle); NDAL MFG Inc., 80 Garden Court, Suite 100, Monterey, CA 93940 (carton); UPC 8 58631 002
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0320-2021·2021-03-03

    Barbara's Orchard Panang Curry Sauce Recalled for Undeclared Shrimp Allergen

    Barbara's Orchard/Delicae Gourmet is recalling Panang Curry Sauce because it contains undeclared shrimp. Consumers with shrimp allergies should not consume the product.

    Product
    Panang Curry Sauce, 12 fl. oz. (355ml), UPC code #643558406711
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0278-2021·2021-03-03

    Teva Recalls Toposar Etoposide Injection Due to Sterility Assurance Issues

    Teva Pharmaceuticals is recalling Toposar (etoposide) injection vials because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    Toposar (etoposide injection USP), 1 gram/50 mL (20 mg/mL), 50 mL Multiple-dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-5657-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0279-2021·2021-03-03

    Teva Recalls Vecuronium Bromide Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of Vecuronium Bromide for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    Vecuronium Bromide for Injection, 10 mg, 1 mg/mL when reconstituted to 10 mL, 10 mL Vial (NDC 0703-2914-01), packaged in 10 x 10 mL Vials per tray (NDC 0703-2914-03), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0276-2021·2021-03-03

    Teva Recalls Leucovorin Calcium Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.

    Product
    Leucovorin Calcium for Injection, USP, 100 mg/vial, Single-Dose Vial, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-5140-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0280-2021·2021-03-03

    Teva Recalls Epoprostenol Sodium Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    Epoprostenol Sodium for Injection, 1.5 mg/vial (1,500,000 ng), 10 mL vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-1995-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0281-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, 1 mL Single-Dose Vial (NDC 0703-0051-01), packaged in 25X1ML vials per tray (NDC 0703-0051-04), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0275-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL, 1 mL Single-Dose Vial (NDC 0703-0031-01), packaged in 25X1ML per tray (NDC 0703-0031-04), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0317-2021·2021-03-03

    Aaron's Gourmet Smoked Fish Recalled for Potential Botulism Risk

    Aaron's Gourmet Smoked Fish is being recalled due to potential Clostridium botulinum contamination. The products were produced and sold without licensure or regulatory oversight.

    Product
    Aaron's Gourmet Smoked Fish (King, Sockeye, or Steelhead) packaged in glass jars or in vacuum plastic bags. The label on GLASS JAR is read in parts: "***AARON'S GOURMET SMOKED FISH ***Portland Oregon (503) 372-9849 ***Quinault Tribal Seafoods ***Traditional Native American Smo
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0272-2021·2021-03-03

    Teva Recalls Desmopressin Acetate Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Desmopressin Acetate Injection because manufacturing areas exceeded microbial limits, compromising sterility assurance.

    Product
    Desmopressin Acetate Injection USP, 4 mcg/mL, 1 mL Preserved Vial (NDC 0703-5051-01), packaged in 10X1 mL Vials per Tray (NDC 0703-5051-03), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0273-2021·2021-03-03

    Teva Recalls Sterile Diluent for Epoprostenol Sodium Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of Sterile Diluent for Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    Sterile Diluent for Epoprostenol Sodium for Injection, 50 mL vial (NDC 0703-9258-01), packaged in 2X50ML per tray (NDC 0703-9258-09), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0285-2021·2021-03-03

    Teva Recalls Leucovorin Calcium Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    Leucovorin Calcium for Injection, USP, 350 mg/vial, Rx only, labeled as a) Teva Parenteral Medicines, Inc., Irvine, CA 92618, and b) Manufactured By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, novaplus+, NDC 0703-5145-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0277-2021·2021-03-03

    Teva Recalls Metoclopramide Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Metoclopramide Injection because manufacturing areas exceeded microbial acceptance levels, creating a lack of sterility assurance.

    Product
    METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V131000·2021-03-03

    Porsche Recalls Macan Models Due to Front Passenger Air Bag Sensor Defect

    Porsche is recalling certain 2015-2018 Macan models because the front passenger seat occupancy sensor may fail to detect a passenger, preventing the air bag from deploying.

    Product
    PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN, MACAN GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1138-2021·2021-03-03

    DeRoyal Recalls Non-Sterile Sternum Saw Blades in Surgical Packs

    DeRoyal Industries is recalling 309 CV Basin Set Packs because the included sternum saw blades are not sterile.

    Product
    CV Basin Set Pack, REF numbers: a) 89-7935.11 b) 89-7935.12 c) 89-7935.13 d) 89-7935.14 e) 89-7935.15 f) 89-7935.16 Custom surgical procedure packs including sternum saw blades.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0283-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling 6,710 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 200 mg/5 mL (0 mg/mL), 5 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0043-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0282-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0045-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0284-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling 15,043 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/5 mL (80 mg/mL), 5 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0063-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0267-2021·2021-03-03

    CareFusion Recalls ChloraPrep Antiseptic Applicators for Potential Fungal Contamination

    CareFusion 213, LLC is recalling ChloraPrep One-Step antiseptic applicators distributed in Puerto Rico and Oman due to potential fungal growth and package integrity breaches in hot, humid climates.

    Product
    ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution -Clear, 0.10 fl. oz. (3ml) each, 25 applicators per carton. CareFusion El Paso, TX 79912, NDC 054365-400-01 Cat. No. 260400
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0265-2021·2021-03-03

    FDA Recalls Chloraprep One-Step Due to Potential Fungal Growth

    CareFusion 213, LLC is recalling Chloraprep One-Step applicators distributed in Puerto Rico and Oman due to potential fungal growth in hot, humid conditions.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0316-2021·2021-03-03

    Golden Boy Custard Muffin Banana Recalled for Undeclared Milk

    Hong Thai Foods Corp is recalling Golden Boy Custard Muffin Banana packages due to undeclared milk discovered during New York state sampling.

    Product
    Golden Boy Custard Muffin Banana 220 grams/7.76 ounce packages
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0274-2021·2021-03-03

    Teva Recalls Epoprostenol Sodium Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    Epoprostenol Sodium for Injection, 0.5 mg/vial (500,000 ng), 1X10ML vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-1985-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2021·2021-03-03

    FDA Recalls Chloraprep One-Step Antiseptic Due to Non-Sterility Risk

    CareFusion 213, LLC is recalling 400 cartons of Chloraprep One-Step antiseptic applicators distributed in Puerto Rico and Oman due to potential fungal growth and package integrity breaches.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0322-2021·2021-03-03

    Thai Peanut Sauce Recalled for Undeclared Shrimp Allergen

    Barbara's Orchard/Delicae Gourmet is recalling Thai Peanut Sauce due to undeclared shrimp. Consumers should stop using the product and return it to the store.

    Product
    Thai Peanut Sauce, 12 fl. oz. (355ml), UPC code #643558406919
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0271-2021·2021-03-03

    Teva Recalls Dacarbazine Injection Due to Sterility Assurance Concerns

    Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.

    Product
    Dacarbazine for Injection USP, 200 mg, Single Use Vial (NDC 0703-5075-01), packaged in 10X20 ML Single Use Vials per tray (NDC 0703-5075-03); Rx only, TEVA Pharmaceuticals USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0321-2021·2021-03-03

    Spicy Red Curry Sauce Recalled for Undeclared Shrimp Allergen

    Barbara's Orchard/Delicae Gourmet is recalling Spicy Red Curry Sauce due to an undeclared shrimp allergen. Consumers should check their pantry for the affected batches.

    Product
    Spicy Red Curry Sauce, 12 fl. oz. (355ml), UPC code #643558406810
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0266-2021·2021-03-03

    CareFusion Recalls Non-Sterile ChloraPrep Solution Due to Microbial Contamination Risk

    CareFusion 213, LLC is recalling non-sterile ChloraPrep With Tint solution distributed in Puerto Rico and Oman due to potential fungal contamination.

    Product
    ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution - Hi-Lite Orange, 0.10 fl. oz. (3 ml) each, 25 applicators in carton, CareFusion El Paso, TX 79912, NDC 054365-400-11 Cat. No. 260415
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1145-2021·2021-03-03

    Smiths Medical Recalls Bivona Cuffless FlexTend Tracheostomy Tubes Due to Packaging Error

    Smiths Medical is recalling specific lots of Bivona Cuffless FlexTend Tracheostomy Tubes because they may have been packaged with the wrong neck flange, posing a risk of patient injury.

    Product
    Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots 3991171, 3991172, and 3988103) V Neck Flange 4.5mm - Product Usage: intended to provide direct airway access for a tracheotomized patient for up to 29 days. It ma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V133000·2021-03-03

    Altec Recalls 2017-2019 Wood Chippers Due to Exhaust Leak Fire Risk

    Altec is recalling 2017-2019 DC1317 and DRM12 wood chippers because a flexible exhaust pipe section may separate, creating an exhaust gas leak that increases the risk of a fire.

    Product
    ALTEC — ALTEC DC1317 CHIPPER, DRM12 WOOD CHIPPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0324-2021·2021-03-03

    Litehouse Recalls Brite Harbor Caesar Dressing Due to Undeclared Anchovies

    Litehouse Inc is recalling Brite Harbor Caesar Dressing & Dip because the product contains undeclared anchovies, a potential allergen.

    Product
    Brite Harbor Caesar Dressing & Dip, 1.5 oz pillows (pouches), item # 16002. The front label states "***BRITE HARBOR CAESAR DRESSING & DIP***" and the back label states "***BLUE CHEESE DRESSING***CONTAINS Egg, Milk ***".
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0323-2021·2021-03-03

    Dole Chopped Kit Sunflower Crunch Recalled for Undeclared Allergens

    Dole Fresh Vegetables Inc. is recalling Dole Chopped Kit Sunflower Crunch due to potential undeclared wheat and tree nuts.

    Product
    Dole Chopped Kit- Sunflower Crunch Cabbage, Green Leaf Lettuce, Kale, Sunflower Seeds, Sweet Onion and Citrus Dressing, Bacon Crumbles, Red Cabbage, Green onions, carrots. UPC: 0 71430 00034 2 Salad and Toppings Net Wt.:9.5 oz. (269 g) Dressing 2.4 fl oz.(72 mL) Total Net Wt.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0309-2021·2021-03-03

    Publix Steam in Bag Green Bean Butternut Squash Recalled for Listeria

    Publix is recalling Steam in Bag Green Bean Butternut Squash because the butternut squash used in its preparation is potentially contaminated with Listeria monocytogenes.

    Product
    Publix Steam in Bag Green Bean Butternut Squash
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1147-2021·2021-03-03

    Northgate Recalls ConMed Abdominal Insufflators Due to Incorrect Tubing Material

    Northgate Technologies is recalling 25 ConMed 50L abdominal insufflators because an internal tubing component was made with untested material.

    Product
    ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum) to allow the insertion of a variety of surgical instruments through the abdominal wall for visual examination of the interior or fo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0308-2021·2021-03-03

    Publix Steam in Bag Season Butternut Medley Recalled for Listeria Risk

    Publix Super Markets is recalling Steam in Bag Season Butternut Medley because the butternut squash used in its preparation is potentially contaminated with Listeria monocytogenes.

    Product
    Publix Steam in Bag Season Butternut Medley
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1148-2021·2021-03-03

    Northgate Recalls Steris CO2MPACT Endoscopic Insufflator Systems Due to Tubing Material Error

    Northgate Technologies is recalling 45 Steris CO2MPACT Endoscopic Insufflator systems because an internal tubing component was made with incorrect, untested material.

    Product
    Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1140-2021·2021-03-03

    DeRoyal Heart Pack Recall Due to Non-Sterile Sternum Saw Blades

    DeRoyal Industries is recalling Heart Packs containing non-sterile sternum saw blades. The affected surgical saw blades are marked with a green non-sterile sticker.

    Product
    Heart Pack, REF numbers: a) 89-9194.07 b) 89-9194.09 c) 89-9194-10 d) 89-9194-11 Custom surgical procedure packs including sternum saw blades.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0310-2021·2021-03-03

    Publix Steam in Bag Butternut Brussels Pecan Recalled for Listeria Risk

    Publix Super Markets is recalling Steam in Bag Butternut Brussels Pecan because the butternut squash used in its preparation is potentially contaminated with Listeria monocytogenes.

    Product
    Publix Steam in Bag Butternut Brussels Pecan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0318-2021·2021-03-03

    Harry & David Chocolate Cherries Recalled for Undeclared Cashews and Almonds

    Harry & David is recalling specific lots of Chocolate Cherries due to undeclared cashews and almonds. Consumers should stop eating the product and return it for a refund.

    Product
    Harry & David brand Chocolate Cherries packaged in a clear 3 oz (85g) bag, UPC 7 80994 32341 4. This product is part of the Premium Delights Gift Box, Founders Favorites Gift Box, Valentine s Day Sweets Box, and Tower of Treats¿ Valentine s Day Gift. The Chocolate Cherries
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1143-2021·2021-03-03

    Natus EDS 3 CSF External Drainage System Recalled for Pyrogen Test Failure

    Natus Manufacturing Limited is recalling 7 units of the EDS 3 CSF External Drainage System because the device failed to meet pyrogen test requirements for endotoxins.

    Product
    Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product Usage: indicated for draining cerebrospinal fluid (CFS) from the cerebral ventricles or the lumbar subarachnoid space as a means of reducing intracranial pressure and CSF volume when the insertion of a permanent,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1139-2021·2021-03-03

    DeRoyal Open Heart Packs Recalled Due to Non-Sterile Sternum Saw Blades

    DeRoyal Industries is recalling 1,084 Open Heart Packs because the included sternum saw blades were not sterile, despite being part of a surgical procedure pack.

    Product
    Open Heart Pack, REF numbers: a) 89-7483.07 b) 89-7483.08 c) 89-7483.09 d) 89-7483.10 Custom surgical procedure packs including sternum saw blades.
    Category
    Medical Device
    Distribution
    3 states
  • HighCPSC·21090·2021-03-03

    Haro Recalls Masi Bicycles Due to Fork Steerer Tube Breakage Hazard

    Haro Bicycles is recalling approximately 510 Masi Evoluzione and Gran Corsa bicycles from model years 2017-2020 because the fork steerer tube can break, causing riders to lose control and fall.

    Product
    Model Year 2017-2020 Masi Evoluzione and Gran Corsa bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1137-2021·2021-03-03

    Respironics Recalls 94 Philips Ventilator Batteries Due to Design Verification Issues

    Respironics is recalling 94 Philips V60 ventilator batteries because they were shipped without proper design verification. The recall covers distribution across multiple U.S. states.

    Product
    PHILIPS BATTERY, V60 14.4V, 11.0 Ah, 163 Wh, REF 1076374(1058272), LOT M94663-P1 - Product Usage: The ventilator is intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V132000·2021-03-03

    2021 Volkswagen Atlas Wheels May Separate Due to Machining Defect

    Volkswagen is recalling certain 2021 Atlas and Atlas Cross Sport vehicles due to improperly machined wheel lug bolt holes that may prevent wheels from attaching properly, risking wheel separation and crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1141-2021·2021-03-03

    Ecolab Recalls Slush and Warmer Disc Drapes Due to Sterile Barrier Risk

    Ecolab is recalling specific lots of ORS-320 Slush + Warmer Disc Drapes because manufacturing slits may breach the sterile barrier, posing an infection risk to patients.

    Product
    Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover intended for use during various surgeries where warm irrigation, slush and/or cold solution is required.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0329-2021·2021-03-03

    Coolhaus Dairy Free Mocha Marcona Almond Fudge Recalled for Undeclared Soy

    Coolhaus is recalling 432 units of Dairy Free Mocha Marcona Almond Fudge because soy lecithin was not declared on the label.

    Product
    Coolhaus Awesome Dessert - Dairy Free Mocha Marcona Almond Fudge, Creamy Coffee Fudge Swirl & Marcona Almond Frozen Dessert. 16 fl.oz, Dessert Paperboard Pint (473 mL) UPC: 851916003605 Coolhaus Headquarters, Culver City, CA Contains Statement: Tree nuts, Coconut
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1136-2021·2021-03-03

    Ortho-Clinical Recalls Deformed VITROS Chemistry VersaTips

    Ortho-Clinical Diagnostics is recalling deformed VITROS Chemistry VersaTips that may cause assay results to be biased by up to +/-16%.

    Product
    VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and reagent fluid for MicroWell assays. In addition, VersaTips are used to dispense R1 Reagent Fluid into cuvettes in combination with sample fluid for Micro Tips Assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1142-2021·2021-03-03

    Recall of Parietex Hydrophilic Anatomical Mesh Due to Incorrect Side Labeling

    Covidien is recalling Parietex hydrophilic anatomical mesh where the package label indicates left-side use but contains a right-side device. This labeling error can lead to implant failure and hernia recurrence.

    Product
    Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0311-2021·2021-03-03

    Water Gardens Confections Recalls Macey's Kong Popcorn Due to Plastic Fragments

    Water Gardens Confections LLC is recalling 7,736 bags of Macey's Kong Popcorn found in Utah because small plastic fragments were discovered in the packaging.

    Product
    Macey's Kong Popcorn, 24 oz., in plastic zip pouch. UPC: 0-41172-00046-7, Manufactured By: Water Gardens Confections, LLC, Orem, Utah, 84057.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0288-2021·2021-03-03

    Fludeoxyglucose F 18 Injection Recalled for Lack of Sterility Assurance

    The General Hospital Corporation is recalling Fludeoxyglucose F 18 Injection due to a lack of assurance of sterility. The product was distributed to one direct account.

    Product
    FLUDEOXYGLUCOSE F 18 — FLUDEOXYGLUCOSE F 18 (FLUDEOXYGLUCOSE F-18)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0287-2021·2021-03-03

    Dr. Reddy's Recalls Imatinib Mesylate Tablets for Dissolution Failures

    Dr. Reddy's Laboratories is recalling specific lots of Imatinib Mesylate 100mg tablets because they failed to meet required dissolution specifications.

    Product
    IMATINIB — IMATINIB (IMATINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1144-2021·2021-03-03

    Siemens ARTIS Icono Biplane and Floor Systems Recalled for Software Errors

    Siemens is recalling 41 ARTIS Icono systems with software version VE20B due to misleading error messages and manual gaps that may cause procedure termination.

    Product
    ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700 with software version VE20B - Product Usage: Intended for single and biplane diagnostic imaging and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0270-2021·2021-03-03

    Areva Pharmaceuticals Recalls Irinotecan Hydrochloride Injection Due to CGMP Deviations

    Areva Pharmaceuticals is recalling 3,287 vials of Irinotecan Hydrochloride Injection due to manufacturing quality deviations identified in a Warning Letter.

    Product
    Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 2 mL Single-Dose Vial, Rx Only, Distributed by: Areva Pharmaceuticals, Inc., Gerogetown, IN 47122, Made in India, NDC 59923-714-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0338-2021·2021-03-03

    Tropical Nut & Fruit Recalls Milk Chocolate Peanuts for Mislabeling

    Tropical Nut & Fruit Inc is recalling 7,200 units of Milk Chocolate Double Dipped Peanuts due to undeclared peanuts on the packaging.

    Product
    Milk Chocolate Double Dipped Peanuts No Brand Name 7.5oz Non-Flex Plastic Tub
    Category
    Food
    Distribution
    0 states
  • LowFDA (Food)·F-0319-2021·2021-03-03

    House Autry Tartar Sauce Recalled Due to Spoilage Complaints

    House-Autry Mills is recalling 9-ounce bottles of tartar sauce after a consumer reported the product was spoiled.

    Product
    HOUSE AUTRY TARTAR SAUCE NET WT 9 OZ (255g) DISTSRIBUTED BY House -Autry Mills, Inc. Four Oaks, NC 27524 UPC 0 73484 60013 4
    Category
    Food
    Distribution
    6 states
  • LowFDA (Devices)·Z-1135-2021·2021-03-03

    Medline Recalls STAT-Site B-HB Controls Due to Shipment Compromise

    Medline Industries is recalling specific lots of STAT-Site B-HB controls because the products were compromised during shipment. The recall affects 46 units distributed in Mississippi, Ohio, and Illinois.

    Product
    S-O303000 CONTROL, STAT-SITE B-HB, 2X3ML,1LOW,1HIGH - Product Usage: intended for the quantitative determination of the ketone body ¿-Hydroxybutyrate in serum or plasma. For laboratory use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V130000·2021-03-02

    Ferrara Recalls 2009-2020 Aerial Vehicles Due to Trolley Defect

    Ferrara is recalling 2009-2020 Aerial vehicles because a defective waterway trolley can detach and fall, posing a risk of injury or death.

    Product
    FERRARA — FERRARA AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2021·2021-03-01

    Milky Way Recalls Canned Corned Beef Imported Without Inspection

    Milky Way International Trading Corp. is recalling approximately 297,715 pounds of canned corned beef products that were imported and distributed in the U.S. without FSIS import re-inspection.

    Product
    Milky Way International Trading Corp. Recalls Canned Corned Beef Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V127000·2021-03-01

    Hyundai Recalls Kona and Ioniq Electric Vehicles for Battery Fire Risk

    Hyundai is recalling 2019-2020 Kona Electric and 2020 Ioniq Electric vehicles because the lithium-ion battery may short-circuit, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI KONA ELECTRIC, IONIQ ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide

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