The Recall Desk

Archive

April 2023 recalls

411 recalls were announced in April 2023.

What the numbers show

Critical
6
Severe
53
High
277
Moderate
71
Low
4

Of the 411 recalls this month scored against our rubric, 1% are Critical, 13% are Severe.

1–100 of 411

  • HighNHTSA·23V305000·2023-04-28

    Ford Explorer backup camera display failure reduces rear visibility

    Certain 2020-2022 Ford Explorer Police Interceptor Utility vehicles have a software issue where the backup camera display does not appear when turned off before reversing, reducing rear visibility and increasing crash risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V307000·2023-04-28

    Winnebago Motorhomes Recalled for Improperly Secured Fuel Hose

    Winnebago is recalling certain 2020-2023 motorhomes due to unsecured fuel hoses that can leak gasoline and increase fire risk. Owners should contact dealers for free inspection and replacement.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, EKKO, SOLIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E036000·2023-04-27

    Chrysler Recalls Mopar Hybrid Battery Packs Due to Fuse Fastener Defect

    Chrysler is recalling Mopar hybrid battery packs because incorrect fasteners may cause excessive heat, leading to power loss and increased crash risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23750·2023-04-27

    Pool Drain Covers Recalled for Entrapment Hazard

    Vijayli-US is recalling about 116 round pool drain covers sold online that do not meet Virginia Graeme Baker Pool and Spa Safety Act standards, posing an entrapment hazard to swimmers and bathers.

    Product
    Pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23191·2023-04-27

    EGL Motor ACE Youth ATVs Fail Safety Standards; Risk of Injury or Death

    EGL Motor is recalling about 4,000 ACE-branded youth all-terrain vehicles (ATVs) that fail federal safety standards. The K125 and C125 models exceed maximum speed limits, and the T125 and C125 models have faulty parking brakes, posing risks of high-speed crashes and collisions.

    Product
    EGL Motor ACE-branded Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V301000·2023-04-27

    2020 RAM ProMaster Transmission Park Pawl Defect Risks Vehicle Rollaway

    RAM is recalling certain 2019-2021 ProMaster vehicles due to debris in the transmission that can prevent the park pawl from fully engaging. This may result in vehicle rollaway, increasing crash and injury risk.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23192·2023-04-27

    Easter Bunny and Butterfly Jewel Necklaces Recalled for High Cadmium

    Creative Education of Canada is recalling about 4,300 Easter Bunny and Boutique Butterfly Jewel Necklaces sold nationwide and online from January through March 2023 due to high levels of cadmium, which is toxic if ingested by children.

    Product
    Easter Bunny and Boutique Butterfly Jewel Necklaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23748·2023-04-27

    Pool and Spa Drain Covers Recalled for Entrapment Hazard Violation

    Pickloud-US has recalled approximately 100 round pool and spa drain covers sold on Amazon because they do not meet entrapment protection standards under the Virginia Graeme Baker Pool and Spa Safety Act, posing an entrapment hazard to swimmers and bathers.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23749·2023-04-27

    Ejoyous Pool Drain Covers Recalled for Entrapment Hazard

    Ejoyous pool drain covers sold online do not meet Virginia Graeme Baker Pool and Spa Safety Act standards and pose an entrapment hazard to swimmers and bathers.

    Product
    Ejoyous pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23190·2023-04-27

    Black Diamond Recon LT Avalanche Transceivers Recalled for Communication Loss Risk

    Black Diamond is recalling about 1,550 Recon LT avalanche transceivers because they can unexpectedly enter search mode due to beacon interference, potentially failing to transmit a skier's position during an avalanche rescue.

    Product
    Recon LT Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V303000·2023-04-27

    2022-2023 Jeep Wrangler Plug-In Hybrid Battery Fuse Fastener Defect

    Chrysler is recalling certain 2022-2023 Jeep Wrangler PHEVs due to incorrect fasteners in the high voltage battery pack that can cause excessive heat and potential loss of drive power, increasing crash risk.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23189·2023-04-27

    Vornado Recalls Travel Steam Irons for Fire, Burn, and Shock Hazards

    Vornado is recalling approximately 317,000 Steamfast and Brookstone travel steam irons because the power cord can become damaged near the bushing, creating fire, burn, and electrical shock hazards. No injuries have been reported.

    Product
    Steamfast Home & Away Travel Steam Irons and Brookstone Steam Bug Travel Steam Irons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23194·2023-04-27

    Diamond Visions Recalls Screaming Plush Monkey Toys for Choking Hazard

    Diamond Visions is recalling about 6,000 Screaming Plush Monkey Toys because the eyes can detach, creating a choking hazard for children. No injuries have been reported.

    Product
    Screaming Plush Monkey Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0736-2023·2023-04-26

    Kagome Worchester Sauce Recalled for Undeclared Soy Allergen

    Kagome Worchester Sauce in 16.9 fl. oz plastic bottles is recalled because it contains soy that is not declared on the label, posing a risk to consumers with soy allergies.

    Product
    Kagome Worchester Sauce 16.9 fl., oz plastic bottles
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0739-2023·2023-04-26

    Food Recall: HyVee Hamburger Chili Macaroni Skillet Meal – Undeclared Milk

    HyVee Hamburger Chili Macaroni Skillet Meal (5.2oz) is recalled due to undeclared milk allergen. The product was voluntarily recalled by the manufacturer and is no longer in distribution.

    Product
    HyVee Hamburger Chili Macaroni Skillet Meal, 5.2oz retail carton. UPC: 0 75450-08552 5
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1357-2023·2023-04-26

    Shiley Adult Flexible Tracheostomy Tubes Recalled Due to Undersized Connectors

    Covidien is recalling Shiley Adult Flexible Tracheostomy Tubes due to undersized connectors that create loose connections with 15mm respiratory circuit components. Unsecure connections could cause respiratory failure, difficulty breathing, treatment delays, or serious injury.

    Product
    Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner Cannula (REF, Product Description): 10CN10H, 10.0MM SHILEY CUFFED TRACH CAN; 10CN10R, 10.0MM ADT FLEX TRACH W TG CUFF; 10UN10A, 10.0MM UNCUFF TRACH TUBE X1;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0737-2023·2023-04-26

    Kagome Chuno Sauce recalled for undeclared soy allergen

    North American Food Dist. Co., Inc. is recalling Kagome Chuno Sauce 16.9 fl. oz bottles (UPC 4901306097519) due to undeclared soy. Approximately 125 bottles were distributed in CA, CO, and NV.

    Product
    Kagome Chuno Sauce 16.9 fl., oz plastic bottles
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·23V295000·2023-04-26

    BMW iX and i4 vehicles recalled for battery monitoring circuit defect

    BMW is recalling certain 2022-2024 iX xDrive50 and 2023 i4 models due to improperly secured electrical connections in the battery monitoring circuit, which can cause engine stall and increase crash risk.

    Product
    BMW — BMW IX, I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0738-2023·2023-04-26

    Sheila G's Gluten Free Reese's Pieces Brownie Brittle recalled for undeclared wheat

    Sheila G's Gluten Free Reese's Pieces Brownie Brittle (4 oz bags, UPC 711747 011562) is being recalled because the product may contain undeclared wheat despite its gluten-free label, creating a risk for consumers with celiac disease or wheat allergies.

    Product
    Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC 711747 011562)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0734-2023·2023-04-26

    Volupta Organic Black Chia Seeds Recalled for Salmonella

    NSI Group LLC is recalling 1,351 pouches of Volupta Organic Black Chia Seeds distributed to a Costco location in San Diego, CA, due to Salmonella detected in product testing.

    Product
    Volupta Organic Black Chia Seeds 64 oz. Best By: 10/31/2025 Stand up pouch. Product of Paraguay
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0741-2023·2023-04-26

    Matiz Piparra Peppers Recalled Due to Glass Contamination

    Power Selles Imports is recalling Matiz Piparra Peppers due to glass contamination. A shard of glass was found in one jar. Consumers should not consume the affected product.

    Product
    Matiz Piparra Peppers are packaged in a clear glass jar, net wt. 4lb. (1.8kg), drained wt. 25oz (700g). Product is shelf stable. UPC 832924005768. Produced By Conservas Rubio - Navarra, Spain. Imported By Matiz A Culinary Collective Company Lynnwood, WA.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1407-2023·2023-04-26

    Surgical Centurion CirClamp Recalled for Incorrect Subassembly Size

    Medline Industries is recalling 162 units of Centurion CirClamp surgical devices due to incorrect subassembly size. The defect could affect proper device function during surgical use.

    Product
    Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1393-2023·2023-04-26

    Smith & Nephew Knee Implant Component Mispack: Wrong Size Distributed

    Smith & Nephew is recalling 12 JOURNEY II UNI Tibia Insert components due to a manufacturing mispack. Some boxes incorrectly contain a different size component.

    Product
    JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1400-2023·2023-04-26

    FDA Recalls MectaLIF ANTERIOR Spinal Fusion Device Due to Screw Breakage Risk

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR Lag Plate Flush H10 interbody fusion device due to a potential risk of screw breakage in the anti-backout plate. No injuries have been reported.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1419-2023·2023-04-26

    Beckman Coulter Free T3 Reagent Test Kit Recalled for Falsely Elevated Results

    Beckman Coulter is recalling Access Free T3 reagent test kits (Catalog #A13422, Lot #233968) because approximately 15-20% of samples produce falsely elevated results that could lead to misdiagnosis and inappropriate thyroid treatment.

    Product
    Beckman Coulter Access Free T3, Triiodothyronine, Free, Catalog #A13422, each box contains 2 reagent packs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1403-2023·2023-04-26

    FDA Recalls MectaLIF ANTERIOR Interbody Fusion Device Due to Screw Breakage Risk

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR interbody fusion device due to potential breakage of the small screw that affixes the anti-backout plate. The recall affects 34 units distributed in the United States.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-0735-2023·2023-04-26

    Tried and True Granola recalled for undeclared milk allergen

    Bakery Barn has recalled Tried and True Granola products due to undeclared milk allergen. The recall affects 690 units distributed to retailers in Ohio and Pennsylvania.

    Product
    Tried and True Granola Co. Naturally Sweetened Granola packaged in 20lb bulk plastic bags and 14oz plastic containers
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0538-2023·2023-04-26

    Compounded Semaglutide Injection Recalled Due to Sterility Assurance Failure

    Vital Care Compounder is recalling C-Semaglutide 5mg/mL injection in 0.5mL vials due to lack of assurance of sterility. The recall affects 45 vials distributed in Mississippi.

    Product
    C-Semaglutide 5mg/mL injection, 0.5mL vials, Rx only, Vital Care Compounder 115 South 40th Ave, Suite A Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1409-2023·2023-04-26

    Spinal implant screws recalled due to defective titanium material

    Medtronic is recalling 45 units of INFINITY Multi-Axial Screws (lot H5802983) worldwide because incorrect titanium was used, reducing the screw head's gripping strength. No illnesses or injuries have been reported.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 24mm, REF 3604024; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0748-2023·2023-04-26

    Trader Joe's Chickenless Crispy Tenders Recalled for Foreign Material Contamination

    Dr. Praeger's Sensible Foods is recalling Trader Joe's Chickenless Crispy Tenders due to potential fibrous contamination. Consumers should discard the product or return it to the retailer.

    Product
    Trader Joe's Chickenless Crispy Tenders Net Wt, 8.1 OZ (230g) UPC 0097 8996 Packaged in a plastic bag
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1415-2023·2023-04-26

    Laboratory diagnostic device software issue may delay clinical diagnosis

    BD Kiestra InoqulA+ (software versions 5.1/5.1.1) fails to display plate information after processing in clinical laboratories, risking diagnostic delays or specimen recollection.

    Product
    BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro diagnostic medical device intended to automate specimen processing according to user-defined procedures and protocols. Catalog (Ref) No. : 447213
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0733-2023·2023-04-26

    Dietary Supplement with Unapproved COVID-19 Treatment Claims Recalled

    Natural Solutions Foundation is recalling a colloidal silver dietary supplement labeled to treat COVID-19. The product violates FDA regulations prohibiting disease claims on dietary supplements.

    Product
    Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0740-2023·2023-04-26

    Jalapeno cheese sticks recalled for plastic foreign material

    Gilman Cheese Corporation is recalling jalapeno cheese sticks due to potential plastic fragments. Consumers should stop eating and discard the affected product.

    Product
    0.6 oz. jalapeno cheese sticks. P.6LGSTICKJL. Cheese sticks are packed in clear plastic pouches with a nitrogen flush. Pouches contain about 150 sticks, with 2 pouches per case. Cases can weigh between 9 lbs. - 11 lbs.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1404-2023·2023-04-26

    Interbody Fusion Device Recalled for Potential Screw Breakage

    Medacta's MectaLIF ANTERIOR fusion device is being recalled due to potential breakage of a small screw used to affix the anti-backout plate. The recall affects 17 units distributed across the US.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighNHTSA·23V298000·2023-04-26

    2023 Kia Sportage and Related Vehicles Instrument Cluster Display Failure

    The instrument cluster display in certain 2023 Kia vehicles may fail to show any information when started, preventing drivers from viewing critical safety data like tire pressure and warning lights. Kia will update the software for free.

    Product
    KIA — KIA TELLURIDE, SOUL, SPORTAGE, NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V294000·2023-04-26

    2023 BMW X7 and XM Recalled for Loose Exhaust-to-Catalytic Converter Fasteners

    BMW is recalling 2023 X7 and XM models due to improperly tightened fasteners connecting the exhaust system to the catalytic converter, which could increase fire risk. Dealers will replace the gasket and tighten fasteners at no charge.

    Product
    BMW — BMW X7, XM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V300000·2023-04-26

    2023 Genesis GV60 Rear Driveshaft Fracture Increases Crash Risk

    2023 Genesis GV60 vehicles with all-wheel drive may have rear driveshafts that fracture, resulting in loss of drive power and increased crash risk. Hyundai will replace the affected driveshafts at no cost to owners.

    Product
    GENESIS — GENESIS GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1420-2023·2023-04-26

    Baxter ExactaMed Oral Dispenser Recalled for Particulate Matter Contamination

    Baxter Healthcare Corporation is recalling the ExactaMed 20 mL Oral Dispenser (Lot B301S356P) because it may contain particulate matter. The recall affects approximately 91,100 units distributed in the US.

    Product
    ExactaMed Oral Dispenser - 20 mL Clear Pharmacy Pack, REF H9387120; Oral medication syringe
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1414-2023·2023-04-26

    Samsung GM85 Digital X-ray Imaging System Arm Latch Failure

    NeuroLogica Corporation recalls 935 Samsung GM85 digital X-ray systems due to a faulty arm latch in the column support that could allow the arm to fall, creating a risk of bodily injury.

    Product
    Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V299000·2023-04-26

    Multiple Freightliner and Western Star Trucks Recalled for Electronic Stability Control Defect

    Daimler Trucks is recalling certain 2020-2024 Freightliner and Western Star trucks with an electronic stability control system that may cause understeering, increasing crash risk. Free tire replacement is being offered.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CLASSIC CASCADIA, CASCADIA, BUSINESS CLASS M2, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2023·2023-04-26

    INFINITY Multi-Axial Spinal Screws Recalled for Titanium Material Defect

    Medtronic is recalling INFINITY Multi-Axial Spinal Screws due to incorrect titanium material used in manufacturing, which reduces the gripping strength of the screw head. The affected screws are used for spinal fusion and stabilization.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 34mm, REF 3604034; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0745-2023·2023-04-26

    Wegmans Chopped Spinach Recalled for Possible Rodent Contamination

    Wegmans brand steam chopped spinach may be contaminated with rodent hair and parts. Affected packages distributed in New York should be discarded or returned.

    Product
    WEGMANS STEAM CHOPPED SPINACH 12/12OZ Poly steam bags
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1402-2023·2023-04-26

    Medacta MectaLIF ANTERIOR spine implant recalled due to screw breakage risk

    Medacta USA is recalling MectaLIF ANTERIOR interbody fusion devices due to a potential for breakage of a small screw that secures the anti-backout plate. The defect affects 44 units distributed across five US states.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-0746-2023·2023-04-26

    Natural Pak Bacon Glaze Mislabeled; Contains Undeclared Coffee Chili Rub

    Victoria Gourmet's Natural Pak Bacon Glaze packages labeled and sold in Ohio actually contain Coffee Chili Rub with undeclared ingredients including mustard, an allergen.

    Product
    Natural Pak brand Bacon Glaze is packaged in 22.9oz (649g), white, cylindrical, plastic containers; Ingredients: Demerara sugar, honey granules, brown sugar, maple sugar, paprika, spices (black pepper, cinnamon, allspice, clove, natural flavors (maple, honey, cinnamon, clove), pa
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1394-2023·2023-04-26

    Radiometer AQURE Software Recall Due to Patient Mix-up Risk

    Radiometer is recalling AQURE laboratory software versions 2.5.2 through 2.6.1 due to a potential issue that could cause patient data mix-ups.

    Product
    AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage analytical devices and operator profiles. The user can associate patient data with test data. The system shows test results. The system receives data from co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1399-2023·2023-04-26

    Tobii Dynavox TD I-110 Speech Device Recalled Over Loose Battery Risk

    The FDA is recalling the Tobii Dynavox TD I-110, a speech-generating device, because the battery may become loose from its housing and potentially be damaged. This affects users worldwide who depend on this device for communication.

    Product
    Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 750567
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2023·2023-04-26

    Spinal Implant Screws Recalled for Defective Titanium Material

    Medtronic is recalling INFINITY spinal implant screws manufactured with incorrect titanium material. The defect reduces the screw's gripping strength, risking implant performance in critical spinal fusion surgery.

    Product
    INFINITY Occipitocervical Upper Thoracic System, PARTIALLY THREADED MULTI AXIAL SCREW, Size: 4.0mm x 22mm, REF 360PT4022; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unctio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0539-2023·2023-04-26

    Antipsychotic Drug Recalled for Failed Quality Control Test

    Ascend Laboratories is recalling 135 bottles of Aripiprazole 20 mg tablets nationwide due to failure of spectroscopic identification testing, indicating the product may not meet established quality standards.

    Product
    ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2023·2023-04-26

    Medtronic INFINITY Spinal Fusion Screws Recalled for Material Defect

    Medtronic is recalling 10 units of INFINITY Multi-Axial Screws distributed in the US and Canada because incorrect titanium material reduces gripping strength in affected lots.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 32mm, REF 3604532; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1397-2023·2023-04-26

    Habib EndoHPB Bipolar RF Catheter Recalled Due to Thermal Injury Risk

    Boston Scientific recalls the Habib EndoHPB Bipolar RF Catheter used in pancreatic and biliary procedures due to inaccurate instructions that could result in excessive energy delivery and thermal injury.

    Product
    Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A radiofrequency (RF) catheter which provides bipolar energy to perform partial or complete ablation of tissue in the pancreatic and biliary tracts. UPN: M00500070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1417-2023·2023-04-26

    Philips 2D Perfusion Medical Imaging Software Recalled for Signal Processing Errors

    Philips is recalling 2D Perfusion diagnostic imaging software due to signal processing errors that can produce inaccurate presentations, potentially affecting clinical decisions.

    Product
    2D Perfusion, release R1.0.x, R1.1.x, R1.2, and R1.2.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0536-2023·2023-04-26

    Verapamil Hydrochloride Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Amerisource Health Services LLC is recalling Verapamil Hydrochloride Extended-Release Tablets 180 mg due to failed dissolution specifications affecting lots 1008622 and 1010026 distributed nationwide.

    Product
    Verapamil Hydrochloride Extended-Release Tablets, USP, 180 mg, 100 Tablets (10 x 10) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-504-01; NDC Unit Dose: 60687-504-11, barcode (01) 003 60687 504 11 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1401-2023·2023-04-26

    Medacta interbody fusion plate device recalled for screw breakage

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR interbody fusion device because the small screw affixing the anti-backout plate may break, potentially compromising device integrity.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1418-2023·2023-04-26

    Olympus Single-Use Endoscopic Clip Fixing Device Recalled for Deployment Failure

    Olympus is recalling single-use rotatable clip fixing devices used in endoscopy procedures. The clips may fail to deploy from the tube sheath during use.

    Product
    Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1392-2023·2023-04-26

    BioFire FilmArray GI Panel Recalled for Potential False Negative Results

    BioFire Diagnostics is recalling FilmArray Gastrointestinal Panel test kits due to a manufacturing issue that may produce false negative results. Affected units may fail to detect gastrointestinal infections.

    Product
    FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems, REF: RFIT-ASY-0116, (30 pouches/kit)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1405-2023·2023-04-26

    Spinal fusion device antibackout screw may break, FDA recalls

    Medacta Usa Inc is recalling MectaLIF ANTERIOR antibackout lag covers due to potential breakage of the small screw that affixes the anti-backout plate. The defect affects spinal fusion procedures in select US states.

    Product
    MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1412-2023·2023-04-26

    Spinal fixation screws recalled for reduced titanium gripping strength

    Medtronic is recalling 90 INFINITY Multi-Axial Screws (Lot H5806345) due to incorrect titanium material that reduces screw head gripping strength. The defect affects 5 batches distributed in the US and Canada.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 26mm, REF 3604026; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1395-2023·2023-04-26

    Instrument Kit Drill Guides Have Incorrect Depth Range

    GEO Instrument Kits for EPS Plates contain drill guides marked with an incorrect depth range (30mm-60mm instead of 10mm-40mm), which could affect surgical implant placement.

    Product
    GEO Instrument Kit for EPS Plate, REF: 70120001, part of the GEO FirstFUSE 1st MTP Joint Arthrodesis Plating System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1398-2023·2023-04-26

    Pressure Therapy System Recalled for Unauthorized Deep Vein Thrombosis Prevention Claim

    Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.

    Product
    REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. Models: DVTREX-U and DVTREX -L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1391-2023·2023-04-26

    KLS E-Coupling Adapter Recalled for Incorrect Product Identifier Code

    Pro-Dex Inc is recalling 199 KLS E-Coupling Adapter devices due to incorrect Unique Device Identifier (UDI) and GTIN codes. The devices were distributed nationwide.

    Product
    KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0747-2023·2023-04-26

    Natural Pak Coffee Chili Rub Contains Undeclared Bacon Glaze Ingredients

    Natural Pak brand Coffee Chili Rub packages contain undeclared Bacon Glaze ingredients including demerara sugar, honey granules, maple sugar, cinnamon, allspice, clove, and parsley. The affected product was distributed in Ohio.

    Product
    Natural Pak brand Coffee Chili Rub is packaged in 22oz (624g), white, cylindrical, plastic containers; Ingredients: Sea salt, ancho chile, brown sugar, espresso beans, hot smoked paprika, mustard, black pepper, coriander, ginger, oregano, chipotle chile, paprika. Contains: mustar
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0537-2023·2023-04-26

    CVS Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CVS-distributed earwax removal drops containing carbamide peroxide are being recalled because the active ingredient may degrade and become subpotent before the labeled expiration date, potentially leaving the product ineffective.

    Product
    Fast Acting Earwax Removal System (carbamide peroxide), 6.5%, 0.5 FL OZ (15 mL) Drops per bottle, OTC, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, CVS Product # 999532, UPC 0 50428 36475 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1406-2023·2023-04-26

    Avanos Ballard Oral Care Swabs recalled for incorrect expiration date labeling

    Avanos Medical is recalling Ballard Oral Care Swabs (codes 12241, 12243, 12251) due to incorrect expiration date labeling. The recall affects 5,475 cases distributed worldwide.

    Product
    Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1396-2023·2023-04-26

    VITROS COVID-19 Antibody Test Calibrators Recalled for Incorrect Calibrator Levels

    Ortho-Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Total N Antibody Calibrators used in COVID-19 testing due to incorrect calibrator levels in Assay Data Disks, which can delay patient test results.

    Product
    VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody Calibrators programmed onto the Assay Data Disks (ADD) Data Release Versions (DRV): DRVs 6213 through 6218 supporting VITROS Calibrators. Product Code: 6199976
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2023·2023-04-26

    Medtronic SenSight Extension Tunneler Kit: manufacturing defect prevents dual-extension passage

    Medtronic recalled approximately 1414 SenSight Extension Tunneler Kits due to a manufacturing defect where dual carriers were machined on only one side, preventing use for passing two extensions simultaneously.

    Product
    Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of extensions for deep brain stimulation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V292000·2023-04-25

    2023 Subaru Impreza Brake Light Switch and Transmission Interlock Defect

    Subaru is recalling certain 2023 Impreza vehicles due to a faulty brake light switch that may illuminate brake lights without pedal application and allow the transmission to shift out of PARK without pressing the brake pedal, creating rollaway and crash risk.

    Product
    SUBARU — SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V293000·2023-04-25

    2022 Indian Chief Dark Horse motorcycles recalled for missing belt guard reflectors

    Indian Motorcycle Company is recalling certain 2022 Indian Chief motorcycles that lack belt guard reflectors, which reduces visibility and increases crash risk. All affected vehicles have been remedied.

    Product
    INDIAN — INDIAN CHIEF BOBBER, CHIEF BOBBER DARK HORSE, CHIEF DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04252023-01·2023-04-25

    Ivars Ready-to-Eat Meat Soup Products Subject to Public Health Alert

    USDA FSIS issued a public health alert for Ivars meat soup products prepared under insanitary conditions. Consumers should not eat these items.

    Product
    Ivars Commissary — FSIS Issues Public Health Alert for Ready-to-Eat Meat Soup Products Due to Possible Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V289000·2023-04-24

    2022 Forest River Columbus fifth wheel: missing riser tube risks tire damage and crashes

    Forest River is recalling approximately 137 2022 Columbus fifth wheel vehicles because the riser tube between the axle hangers was not installed. This creates inadequate tire clearance, risking tire puncture and vehicle crashes.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E035000·2023-04-24

    Dana Spicer Ultimate Dana 60 Axle Recall for Jeep Wrangler

    Dana Incorporated is recalling Spicer Ultimate Dana 60 Bracketless Crate Axles for Jeep Wranglers because a suspension bracket may prevent sufficient lubrication from reaching the pinion tail bearings.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V290000·2023-04-24

    Forest River Recalls 2023 East to West Travel Trailers for Placard Error

    Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because the Federal Placard may display incorrect weight and capacity data.

    Product
    EAST TO WEST — EAST TO WEST SILVER LAKE, DELLA TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V291000·2023-04-24

    2022-2023 Nova Bus LFS Electric Bus Recalled for Battery Coolant Line Defect

    Nova Bus is recalling certain 2022-2023 LFS electric transit buses. The high voltage battery pack coolant line may not be fully seated, risking coolant loss and electrical short circuits that could cause fires.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V288000·2023-04-24

    2023 Forest River Salem and Wildwood Travel Trailers: Brake Wiring Defect

    Forest River is recalling certain 2023 Salem and Wildwood travel trailers because the brakes may be incorrectly wired, resulting in potential loss of brake function and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·015-2023·2023-04-21

    Alef Sausage Recalls Halal Meat and Poultry Sausage Due to Misbranding

    Alef Sausage Inc. is recalling ready-to-eat halal meat and poultry sausage products because they lacked required refrigeration labels, posing a risk of temperature abuse.

    Product
    Alef Sausage — Alef Sausage Inc. Recalls Ready-To-Eat Meat and Poultry Sausage Products Due to Misbranding and Possible Temperature Abuse
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·014-2023·2023-04-21

    Abbyland Foods Recalls Frozen Turkey Sausage Patties Due to Undeclared Soy

    Abbyland Foods is recalling approximately 11,800 pounds of frozen turkey meatballs mislabeled as sausage patties because they contain undeclared soy.

    Product
    Abbyland Foods, Inc. — Abbyland Foods Recalls Frozen Turkey Sausage Patties Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V285000·2023-04-21

    2021-2024 Thor Motor Coach Motorhomes Recalled for Fuel Hose Defect

    Thor Motor Coach is recalling approximately 2,919 motorhomes with fuel hose clamps that may lack adequate clamping force, risking gasoline leaks and fires. Owners should contact dealers for free fuel hose and clamp replacement.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TELLARO, SEQUENCE, RIZE, SCOPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V286000·2023-04-21

    Motorhomes recalled for fuel hose defect in Cummins generators

    Certain 2021-2024 Forest River and Coachmen motorhomes equipped with Cummins Onan generators are affected by a fuel hose defect. The inadequate clamp force may cause a gasoline leak, increasing fire risk.

    Product
    COACHMEN — COACHMEN, FOREST RIVER NOVA, BEYOND, GALLERIA, SUNSEEKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V287000·2023-04-21

    Shred-Tech Recalls MDS-4-33 Trucks Due to Fire Risk

    Shred-Tech is recalling 2021-2023 MDS-4-33 shredding trucks because paper accumulation can overheat and cause a fire.

    Product
    SHRED-TECH — SHRED-TECH MDS-4-33
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·012-2023·2023-04-20

    Weinstein Wholesale Meats Recalls Raw Ground Beef Burger Patties

    Weinstein Wholesale Meats is recalling raw ground beef burger patties due to possible contamination with white neoprene pieces.

    Product
    Weinstein Wholesale Meats Inc — Weinstein Wholesale Meats, Inc. Recalls Raw Ground Beef Burger Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·23184·2023-04-20

    Lil Anglers Children's Fishing Rods Recalled for Excessive Lead Content

    Lil Anglers is recalling approximately 78,500 children's fishing rods sold as Kid Casters No Tangle Combos because they contain lead levels that exceed the federal lead content ban. Lead ingestion can cause adverse health effects in young children.

    Product
    Children's Fishing Rods sold with Kid Casters No Tangle Combos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23187·2023-04-20

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    Changshu Lingshang Trading's NewCosplay children's sleepwear fails to meet federal flammability standards, posing a burn injury risk to children. About 110 units sold on Amazon from October 2021 through May 2022 are affected.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23183·2023-04-20

    DeWALT, Stanley, and Craftsman Fiberglass Sledgehammers Recalled for Detachment Hazard

    Stanley Black & Decker is recalling approximately 2.2 million fiberglass sledgehammers because the head can loosen and detach during use, posing an impact injury hazard. The company has received 192 reports of detachment, including two reported injuries.

    Product
    DeWALT, Stanley and Craftsman Fiberglass Sledgehammers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23188·2023-04-20

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    Taizhou Jiawang Trading Co. is recalling about 868 NewCosplay children's sleepwear garments sold on Amazon from November 2021 through April 2022 because they fail to meet federal flammability standards and pose a burn hazard.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23186·2023-04-20

    DynaDrive Fresh Water Well Pumps Recalled Due to Electric Shock Risk

    Davey Water Products is recalling about 1,060 DynaDrive Fresh Water Well Pumps because inadequate grounding can pose an electric shock hazard. One electrical shock has been reported in Australia; no incidents have been reported in the United States.

    Product
    DynaDrive Fresh Water Well Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23746·2023-04-20

    Children's Robes Recalled for Flammability Standards Violation

    Bagno Milano is recalling about 3,600 children's robes sold online from June 2022 through March 2023 because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V283000·2023-04-20

    2023 Ford Ranger Loose Lug Nuts Recall — Wheel Detachment Risk

    Ford is recalling 1,434 2023 Ranger vehicles due to improperly tightened lug nuts on driver-side wheels. Loose lug nuts may cause wheel detachment while driving, increasing crash risk.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E034000·2023-04-20

    Ecotuned EV Conversion Systems Recalled for Charging Harness Fire Risk

    Les Technologies Ecotuned Inc. is recalling 2018-2023 E85 MK3 EV conversion systems because a defective charging harness connection may short circuit and cause a fire.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ONBOARD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23747·2023-04-20

    Lelinta Multi-Purpose Kids Helmets Recalled for Head Injury Risk

    Lucky Global is recalling about 30 Lelinta Multi-Purpose Kids Helmets sold online at Walmart.com because they do not meet federal safety standards for positional stability and may fail to protect children in a crash.

    Product
    Lelinta Multi-Purpose Kids Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V282000·2023-04-20

    International CV Brake Pressure Switch Fire Risk Recall

    Navistar is recalling 2017-2023 International CV trucks for a brake pressure switch assembly defect that may leak brake fluid and cause an electrical short-circuit, increasing fire risk while driving or parked.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·013-2023·2023-04-20

    Bruno Beef Strips Recalls Pepper and Garlic Snack Sticks for Undeclared Soy

    Bruno Beef Strips is recalling approximately 7,452 pounds of Pepper & Garlic snack sticks because the product contains undeclared hydrolyzed soy protein, a known allergen.

    Product
    Bruno Beef Strips Recalls Beef Strip Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • ModerateCPSC·23185·2023-04-20

    Rollerblade Fury Inline Skates Recalled Due to Fall Hazard

    Rollerblade USA is recalling about 13,400 Fury Inline Skates because the rear brake support can fracture or separate, reducing stability and increasing the risk of falls. No injuries have been reported to date.

    Product
    Rollerblade® Fury Inline Skates and Rollerblade® Fury brake supports
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0705-2023·2023-04-19

    Frozen Organic Strawberries Recalled Due to Hepatitis A Contamination

    Multiple brands of frozen organic strawberries are being recalled due to potential hepatitis A contamination. The recall affects products distributed across the United States.

    Product
    Simply Nature Organic Strawberries, frozen, net wt. 24 oz., 8 packages per case. UPC 4099100256222. Product of Mexico. Distributed by Aldi Batavia, IL Vital Choice Organic Strawberries, frozen, net wt. 16 oz., 20 packages per case. UPC 834297005024. Product of Mexico. Distribut
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0702-2023·2023-04-19

    Organic Strawberries Recalled Due to Hepatitis A Contamination Risk

    California Splendor, Inc. is recalling 30-pound cases of Organic IQF Whole Strawberries due to potential Hepatitis A contamination. The recall affects 202,500 pounds distributed to Oregon and California.

    Product
    30 lb. cases of Organic IQF Whole Strawberries
    Category
    Food
    Distribution
    2 states

Looking for a different month? Back to 2023.