The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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13351–13375 of 27736

  • HighFDA (Devices)·Z-1381-2024·2024-04-03

    Medivance Neonatal ArcticGel Pads Recalled for Reduced Water Flow

    Medivance Inc. is recalling Neonatal ArcticGel Pads due to reduced water flow that may prevent proper heating or cooling performance in neonatal temperature management systems. No injuries have been reported.

    Product
    Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0413-2024·2024-04-03

    Neostigmine methylsulfate injection recalled nationwide due to sterility concerns

    SCA Pharmaceuticals is recalling 1,122 syringes of neostigmine methylsulfate injection nationwide due to inability to assure product sterility. The affected lot is 1223048138 (expiration 1/31/24).

    Product
    neostigmine methylsulfate 5 mg/5 mL Injection, (Concentration = 1mg/mL), 5 mL fill 6 mL Syringe, Rx Only, SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0750-09, Bar Code 70004075009
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0404-2024·2024-04-03

    FDA Recalls HYDROmorphone Injection Cassettes Due to Sterility Concerns

    SCA Pharmaceuticals recalls 256 units of HYDROmorphone HCl injection in Grey CADD Cassettes nationwide due to lack of assured sterility. The affected lot is #1223049529 with expiration date 01/03/24.

    Product
    HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-63, Bar Code 70004030063
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1358-2024·2024-04-03

    Bio-Rad QXDx BCR-ABL diagnostic kit recalled for calibration errors

    Bio-Rad Laboratories is recalling a diagnostic test kit due to incorrect calibrations and controls that may produce inaccurate test results. Patients and healthcare providers should contact the manufacturer.

    Product
    Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0423-2024·2024-04-03

    Succinylcholine chloride injection recalled for lack of sterility assurance

    SCA Pharmaceuticals recalls Succinylcholine Chloride 200 mg/10mL injectable due to lack of assured sterility. The recall affects 8,755 syringes distributed nationwide.

    Product
    SUCcinylcholine Chloride 200 mg/10mL Injection (Concentration = 20mg/mL), 10 mL fill 12 mL Syringe, Rx only, Repackaged by SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0908-12, Bar Code 70004090812
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1388-2024·2024-04-03

    Epix Universal Clip Applier Recalled for Potential Clip Loading Failure

    Applied Medical Resources is recalling the Epix Universal Clip Applier because the device may fail to load the surgical clip after the trigger is actuated. Units were distributed worldwide.

    Product
    Epix Universal Clip Applier, REF: CA500, STERILEEO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V152000·2024-04-03

    Certain Volkswagen Atlas vehicles recalled for airbag deployment delay

    Volkswagen is recalling certain Atlas and Atlas Cross Sport vehicles because corroded electrical contacts in the front door wiring harness may delay airbag deployment during side impacts, increasing the risk of injury.

    Product
    VOLKSWAGEN — 2019 VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0418-2024·2024-04-03

    Phenylephrine HCl Injectable Recalled Nationwide for Lack of Sterility Assurance

    SCA Pharmaceuticals is recalling Phenylephrine HCl Injectable (400 mcg/10 mL) distributed nationwide due to lack of sterility assurance. Affected lot numbers have expiration dates through May 2024.

    Product
    PHENYLephrine HCl 400 mcg/10 mL in 0.9% Sodium Chloride Injection, (Concentration = 40 mcg/mL), 10 mL fill 12 mL Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0811-12, Bar Code 70004081112.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V094000·2024-04-02

    Genesis Vehicles Seat Belt Pretensioners May Explode in Crashes

    Hyundai is recalling Genesis vehicles because front seat belt pretensioners may explode during a crash, potentially projecting metal fragments at occupants. Dealers will secure the pretensioners with a cap at no charge.

    Product
    GENESIS — 2021 GENESIS GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V095000·2024-04-02

    Electra Meccanica Solo G2 and G3 recalled for sudden loss of drive power

    Electra Meccanica is recalling 2019-2023 Solo vehicles due to a defect in the motor controller or battery controller that can cause sudden loss of drive power, increasing crash risk. Owners are being notified and eligible for vehicle repurchase.

    Product
    ELECTRAMECCANICA — 2019 ELECTRAMECCANICA SOLO G2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V093000·2024-04-02

    2020 Nissan Rogue Ignition Key May Collapse While Driving

    Nissan is recalling certain 2020 Rogues and Rogue Sports due to a faulty ignition key that may collapse while driving. The collapse could shut off the engine and prevent airbag deployment in a crash.

    Product
    NISSAN — 2020 NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V092000·2024-04-02

    2023 Honda CR-V Passenger Seat Back Frame Welding Defect

    Honda is recalling 2023 CR-V vehicles due to improper welding of the front passenger seat back frame, which may fail in a crash and increase injury risk.

    Product
    HONDA — 2023 HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V114000·2024-04-02

    Proterra buses recalled for loose steering gearbox securing bolts

    Proterra is recalling 2017-2022 Catalyst and ZX5 buses because steering gearbox securing bolts may loosen due to insufficient adhesive, risking loss of steering control. Owner notifications were sent October 7, 2022.

    Product
    PROTERRA — 2022 PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V007000·2024-04-01

    Peterbilt 579 and Kenworth T680 electronic stability control software defect

    PACCAR is recalling approximately 46 Peterbilt 579 (2022-2023) and Kenworth T680 (2023) vehicles with faulty electronic stability control software that may underestimate vehicle mass, reducing crash prevention performance. Dealers will provide a free software update.

    Product
    PETERBILT — 2022 PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V040000·2024-04-01

    2021-2022 Porsche Cayenne Rear Axle Alignment Safety Recall

    Porsche is recalling 2021-2022 Cayenne vehicles due to potential rear axle misalignment following prior repairs. The defect may cause premature tire wear and increase crash risk.

    Product
    PORSCHE — 2021 PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V041000·2024-04-01

    2022 Forest River Vengeance Trailers Recalled for Incorrect Tire Pressure Labels

    Forest River is recalling certain 2022 Vengeance Fifth Wheel trailers because the tire pressure labels may display incorrect information for the front tires, which could result in under-inflated tires and increase the risk of a crash.

    Product
    FOREST RIVER — 2022 FOREST RIVER VENGEANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V006000·2024-04-01

    2023 Triumph Speed Triple RR Radiator Fan Overheat Recall

    Triumph is recalling 2022-2023 Speed Triple RR and RS motorcycles because the radiator fan may overheat and fail, causing hot coolant to leak or spray and increasing the risk of injury and crash.

    Product
    TRIUMPH — 2023 TRIUMPH SPEED TRIPLE RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V038000·2024-04-01

    2013-2021 Grand Design recreational vehicles recalled for fire hazard

    Grand Design RVs (2013-2021) are recalled for an improperly secured 110-volt refrigerator wire that may cause electrical arcing and fire. Dealers will inspect and replace damaged wiring at no cost.

    Product
    GRAND DESIGN — 2015 GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24175·2024-03-28

    Stateside Bead Supply Magnetic Beads Recalled for Ingestion Hazard

    Stateside Bead Supply is recalling high-powered 5mm magnetic beads sold online from November 2022 through June 2023 because they violate federal magnet safety regulations and pose an ingestion hazard. If swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Magnetic Beads HIGH POWER 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24741·2024-03-28

    Polaris Model Year 2022–2023 Snowmobiles Recalled for Fire Hazard

    Polaris is recalling about 7,000 Model Year 2022–2023 snowmobiles equipped with PATRIOT BOOST engines because the fuel line between the fuel rails can leak, posing a fire hazard. Consumers should stop using the recalled snowmobiles and contact Polaris for a free repair.

    Product
    Model Year 2022-2023 Snowmobiles equipped with PATRIOT BOOST Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24742·2024-03-28

    Forias Pack and Play Mattresses Recalled for Infant Suffocation Hazard

    Forias pack and play mattresses sold on Amazon.com from May through August 2023 violate federal crib mattress safety standards and pose a suffocation hazard to infants. The product is missing required warnings and labels.

    Product
    Forias Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24177·2024-03-28

    BJ's Wholesale Club Recalls Berkley Jensen 72-inch Tiki Torches for Burn Hazard

    BJ's Wholesale Club is recalling about 90,000 Berkley Jensen Citronella 72-inch Tiki Torches because the torch top can break open or fall off while lit, creating a burn hazard. The company has received nine reports of the top breaking or falling, including two burn injuries.

    Product
    Berkley Jensen Citronella 72-inch Tiki Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1077-2024·2024-03-27

    Fresh & Ready Ham Torta Sandwich recalled for Listeria monocytogenes contamination

    Fresh & Ready Foods LLC recalled Fresh & Ready Ham Torta Sandwich (9 oz) due to possible Listeria monocytogenes contamination. The recall affects products distributed in California, Nevada, Utah, and Arizona with use-by dates February 3–22, 2024.

    Product
    Fresh & Ready Ham Torta Sandwich 9 oz UPC 8290690707
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1087-2024·2024-03-27

    Don Pancho Fiesta Sauces Recalled for Listeria Monocytogenes Contamination

    Reser's Fine Foods is recalling Don Pancho Fiesta 3 Pack Everything Sauce due to potential Listeria monocytogenes contamination from recalled Cotija cheese repackaged into these ready-to-eat products.

    Product
    Item # 407034, Don Pancho Fiesta 3 Pack Everything Sauce. Each pack consists of Cilantro Lime Crema, Baja-Style Crema, Chipotle Crema. 3/12oz glass bottles per pack, 6 packs per case. UPC on 3-pack box: 0 71117 00741 1.
    Category
    Food
    Distribution
    16 states