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 the agency’s own highest classification or reported deaths or serious injuries, 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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4601–4625 of 39749

  • SevereFDA (Devices)·Z-1382-2024·2024-04-03

    Surgical Tracecarts Recalled Due to Defective Foley Catheter Component

    DeRoyal Industries is recalling 134 GeoMed Custom Tracecarts distributed in Florida that contain a recalled Foley catheter component. Affected units carry specific lot numbers with expiration dates from February 2024 through May 2025.

    Product
    GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL SURGERY TRACECART
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1374-2024·2024-04-03

    Obsidio Conformable Embolic coils recalled for bowel-ischemia risk

    Boston Scientific recalled 985 Obsidio Conformable Embolic coils because using the aliquot delivery technique for lower GI bleeding poses a high risk of bowel ischemia requiring major surgery.

    Product
    Obsidio Conformable Embolic, Material Numbers (UPN): a) M0013972001010, b) M0013972101010
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1327-2024·2024-04-03

    FDA Recalls Fresenius Catheter Extension Tubing Due to Chemical Leachables

    Fresenius Medical Care is recalling 105,700 stay-safe /Luer Catheter Extension 6 in devices nationwide due to chemical leachables identified in the peroxide cross-linked tubing. FDA classified this as a Class I recall.

    Product
    stay-safe /Luer Catheter Ext. 6 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1285-2024·2024-04-03

    Nimbus Ambulatory Infusion Pump recalled due to multiple failure modes

    InfuTronix is recalling Nimbus Infusion Pump Systems (Nimbus Flex, Nimbus PainPro) due to potential battery failure, system errors, drug leakage, flow rate abnormalities, and housing damage. About 52,328 units are affected nationwide.

    Product
    Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump and components
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0429-2024·2024-04-03

    Treprostinil Injection recalled nationwide due to particulate matter contamination

    Par Pharmaceutical is recalling Treprostinil Injection nationwide due to the presence of particulate matter. This FDA Class I recall affects 466 vials of lot 57014 distributed throughout the United States.

    Product
    Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1324-2024·2024-04-03

    FDA Recalls stay-safe Luer Lock Adapter for Chemical Leachables

    The FDA is recalling approximately 828,954 stay-safe Luer Lock Adapters due to chemical leachables identified in the peroxide cross-linked tubing. The nationwide recall affects all lots of Model Number 050-95003.

    Product
    stay-safe /Luer Lock Adapter 4 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1325-2024·2024-04-03

    Stay-safe Luer Lock catheter extension recalled for chemical leachables

    Fresenius is recalling 663,221 stay-safe Luer Lock catheter extension units nationwide due to chemical leachables (NDL PCBAs) identified in the tubing.

    Product
    stay-safe /Luer Lock Catheter Ext. 12 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1128-2024·2024-04-03

    Roland Tahini Recalled Due to Potential Salmonella Contamination

    Roland Tahini 16 oz jars are being recalled due to potential Salmonella contamination. Consumers should not consume this product and should return it to the retailer or contact Roland Foods, LLC.

    Product
    Roland Tahini; 100% Ground Sesame Seeds; Net WT. 16 OZ. (1 LB.) 454g
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-1101-2024·2024-04-03

    Sunflour Bakery Banana Nut Sweet Bread Recalled for Undeclared Soy and Yellow #5

    Sunflour Bakery Banana Nut Sweet Bread is recalled due to undeclared soy (a major allergen) and undeclared Yellow #5. Consumers with soy allergies should not consume this product.

    Product
    Sunflour Bakery Banana Nut Sweet Bread, 16 oz, clear poly bag
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·24V245000·2024-04-02

    2021 Jayco Redhawk motorhomes recalled for power steering connection defect

    Certain 2021 Jayco Redhawk motorhomes have a defective power steering connection that can cause sudden loss of power steering and brake assist, increasing crash risk. Dealers will replace the defective parts free of charge.

    Product
    JAYCO — JAYCO, ENTEGRA GREYHAWK, ESTEEM, ODYSSEY, GREYHAWK PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V244000·2024-04-01

    2023 Kia Forte: Front Suspension Control Arm Failure Risk

    Kia recalls certain 2023 Forte vehicles because the right front lower control arm may be improperly welded and fail, risking sudden loss of steering control and crashes.

    Product
    KIA — KIA FORTE
    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
  • SevereNHTSA·24V238000·2024-03-28

    Chrysler minivan windshields may not be properly bonded to the vehicle

    Chrysler is recalling certain 2024 Pacifica and Voyager vehicles whose windshields may not have been properly bonded, allowing them to detach during a crash. This fails FMVSS 212.

    Product
    CHRYSLER — CHRYSLER VOYAGER, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V237000·2024-03-28

    Chevrolet Colorado and GMC Canyon front wheel hub bolts may break

    General Motors is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles because front wheel hub bolts may have been over-tightened and damaged during installation.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1078-2024·2024-03-27

    Fresh & Ready Chicken Torta Sandwich Recalled for Listeria Contamination

    Fresh & Ready Foods LLC is recalling Fresh & Ready Chicken Torta Sandwich products (use-by dates 02/03/2024–02/22/2024) due to Listeria monocytogenes contamination. Affected products were distributed to California, Nevada, Utah, and Arizona.

    Product
    Fresh & Ready Chicken Torta Sandwich 9 oz UPC 8290690706
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1082-2024·2024-03-27

    Stonewall Kitchen Gluten Free Doughnut Mix Recalled for Undeclared Wheat

    Stonewall Kitchen is recalling Cinnamon Sugar Doughnut Mix (Gluten Free) with use-by dates of March 9-10, 2025, because units contain undeclared wheat. Consumers with wheat allergies or celiac disease should not consume this product.

    Product
    Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten Free; Net Wt. 18oz (510g); UPC: 1138131332
    Category
    Food
    Distribution
    44 states
  • 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-1089-2024·2024-03-27

    HEB Poblano Caesar Dressing recalled for Listeria monocytogenes contamination

    Reser's Fine Foods is recalling HEB Poblano Caesar Dressing due to Listeria monocytogenes contamination from repackaged Cotija cheese. The recall affects 2495 cases distributed across 16 states.

    Product
    FCF Item 403953, HEB Poblano Caesar Dressing, 12oz. glass bottle, 6 bottles per case. UPC 41220 94807
    Category
    Food
    Distribution
    16 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
  • SevereFDA (Food)·F-1090-2024·2024-03-27

    Costco Southwest Wrap Kit Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Costco Southwest Wrap Kits due to Listeria monocytogenes contamination. The product was distributed across 16 states.

    Product
    FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap Kit, Costco Service Deli, 2/8.15 lbs. Net Wt. 16.31 lbs., UPC 0 13454 38424 4. Costco assembled and sold product as Southwest Wrap with Sauce, item #29433.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1072-2024·2024-03-27

    Dole Chopped Kit Avocado Ranch Recalled for Potential Listeria Contamination

    Dole Chopped Kit Avocado Ranch (UPC 71430000915) is being recalled due to potential contamination with Listeria monocytogenes. The FDA Class I recall affects 50,645 cases distributed across the United States and Canada.

    Product
    Dole Chopped Kit Avocado Ranch UPC 71430000915
    Category
    Food
    Distribution
    25 states
  • SevereNHTSA·24V233000·2024-03-27

    2025 Peterbilt and Kenworth Trucks Recalled Over Steering Gear Defect

    PACCAR is recalling certain 2025 Peterbilt and Kenworth trucks because the steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, T680, T280, T380
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1074-2024·2024-03-27

    Dole Cajun Ranch Chopped Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables is recalling 50,645 cases of Dole Cajun Ranch Chopped Kit UPC 71430002063 due to potential Listeria monocytogenes contamination. The affected product was distributed in 24 U.S. states and Canada.

    Product
    Dole Cajun Ranch Chopped Kit UPC 71430002063
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Devices)·Z-1300-2024·2024-03-27

    FDA Recalls HeartMate II Left Ventricular Assist Systems for Graft Obstruction

    Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.

    Product
    HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide