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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4301–4325 of 36541

  • SevereNHTSA·24V178000·2024-03-06

    Prevost Recalls H3-45 Buses Due to Steering Column Joint Failure Risk

    Prevost is recalling 2022-2023 H3-45 and H3-45 VIP buses because steering column joints may fail, causing loss of steering control and increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1164-2024·2024-03-06

    Medtronic Duet External Drainage System catheter disconnection risk recalled

    Medtronic recalls Duet External Drainage and Monitoring System catheter units (REF 46915) due to potential disconnection from stopcock connectors. Worldwide distribution includes 14,139 units.

    Product
    Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Catheter, REF 46915, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce intracranial pressure and CSF volume.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E021000·2024-03-05

    Lippert Utility Hub Oil Seals Recalled for Brake System Leak Risk

    Lippert is recalling Utility Hub Oil Seals that may leak oil onto brake components, potentially reducing braking ability and increasing crash risk.

    Product
    POWER TRAIN:AXLE HUBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·010-2024·2024-03-02

    Trader Joe’s Chicken Soup Dumplings Recalled for Foreign Matter

    CJ Foods Manufacturing Beaumont Corporation is recalling Trader Joe’s Steamed Chicken Soup Dumplings due to possible contamination with hard plastic from a permanent marker pen.

    Product
    CJ Foods Manufacturing Beaumont Corporation — CJ Foods Manufacturing Beaumont Corporation Recalls Trader Joe’s Chicken Soup Dumplings Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V166000·2024-03-01

    Mercedes-Benz Recalls 2023 Sprinter Vans Due to Wiring Harness Fire Risk

    Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because the main wiring harness may chafe and short circuit, increasing the risk of fire and loss of vehicle control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 2500, SPRINTER 3500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V170000·2024-03-01

    Mercedes-Benz Recalls G-Class Vehicles for Incorrect Air Conditioning Refrigerant

    Mercedes-Benz is recalling 2022-2023 G 550 and AMG G 63 vehicles because the air-conditioning system may contain incorrect refrigerant, which could leak and increase fire risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2024·2024-02-29

    MF Meats Recalls Raw Meat Products Contaminated with Non-Food Grade Oil

    MF Meats is recalling approximately 93,277 pounds of raw meat products that may be contaminated with non-food grade mineral seal oil. The products were shipped to restaurants in New York, Ohio, and Pennsylvania.

    Product
    MF Meats — MF Meats Recalls Raw Meat Products Due to Contamination by a Non-Food Grade Substance
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·24V165000·2024-02-29

    BMW motorcycle front struts can fail causing loss of stability

    BMW is recalling certain 2024 R 1250RT, K 1600GT, K 1600GTL and K 1600B motorcycles because an incorrectly manufactured proportional valve in the front spring strut can loosen and cause strut failure.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B, R 1250 RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24137·2024-02-29

    Camplux Portable Tankless Water Heaters Recalled Due to Fire Hazard

    About 42,000 Camplux portable tankless water heaters can leak gas from the regulator connection, creating a fire hazard. The Home Appliances is offering free repair kits with replacement regulators.

    Product
    Camplux portable tankless water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V164000·2024-02-29

    International truck steering gear teeth can crack causing steering loss

    Navistar is recalling certain 2025 International HV, HX, LT and MV vehicles because an improperly heat-treated steering gear sector shaft can crack or fracture, causing a loss of steering control.

    Product
    INTERNATIONAL — INTERNATIONAL LT, HX, MV, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V163000·2024-02-29

    Land Rover Recalls 2024 Discovery Sport for A-Pillar Bolt Issue

    Land Rover is recalling 2024 Discovery Sport vehicles because a lower A-pillar bolt may be improperly fastened, reducing structural strength and increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1081-2024·2024-02-28

    Surgical ocular pack kits recalled due to saline sterility assurance loss

    Windstone Medical Packaging is recalling 80 Aligned Medical Solutions ocular pack surgical kits because sterility of the included saline cannot be guaranteed.

    Product
    Aligned Medical Solutions, In House Ocular Pack, AMS12947, STERILEEO
    Category
    Medical Device
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-1046-2024·2024-02-28

    Dover Foley catheter kits recalled due to defective supplier components

    Cardinal Health is recalling Dover brand Foley catheter kits due to components recalled by supplier Nurse Assist. Approximately 435,060 units were distributed to the US, Europe, Japan, and Latin America.

    Product
    Dover URINE METER ADD-A-FOLEY TRAY, 200 ML, NEEDLE SAMPLING PORT, DRAIN TUBE, PREP TRAY; Dover UNIVERSAL TRAY, 1000 ML BASIN, PVP SWAB STICKS, PREPPING COMPONENTS, 30 CC PRE-FILLED SYRINGE; Dover URINE DRAINAGE ADD-A-FOLEY TRAY, NEEDLE SAMPLING, A/R, DRAIN TUBE, PREP TRAY, 30 ML
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1043-2024·2024-02-28

    Argyle Suction Catheter Trays with Chimney Valve recalled for defective components

    Cardinal Health is recalling multiple Argyle Suction Catheter Tray models due to defective components. The kits containing these recalled components were distributed in the US, Europe, Japan, and Latin America.

    Product
    Argyle" Suction Catheter Tray with Chimney Valve Sterile Saline 18 Fr/Ch (6.0mm); Argyle" Suction Catheter Tray with Chimney Valve Sterile Saline, 6 Fr/Ch (2.0 mm); Argyle" Graduated Suction Catheter Tray with Chimney Valve Sterile Saline 8 Fr/Ch (2.67 mm); Argyle" Suction Cathet
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1047-2024·2024-02-28

    Dover Foley catheters recalled due to defective supplied components

    Cardinal Health Dover Foley catheters (7,800 units distributed in the US, EMEA, Japan, and Latin America) are being recalled because convenience kits were manufactured with components previously recalled by Nurse Assist.

    Product
    Dover" HYDROGEL COATED LATEX 400 ML U/M FOLEY TRAY, LL, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, CSD; Dover" 100% SILICONE SILVER-HYDROGEL COATED 400ML U/M TEMP SENSE FOLEY TRAY, 16FR (5.3 MM), 5CC, CSD; Dover" 100% SILICONE SILVER-HYDROGEL COATED 400ML U/M TEMP SENSE FOLEY TRAY
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0345-2024·2024-02-28

    Dietary supplement Arize recalled for undeclared pharmaceutical ingredient

    Arize Herbal Dietary Supplement contains an undeclared ingredient (nortadalafil), a pharmaceutical used in FDA-approved male sexual enhancement medications, making it an unapproved drug.

    Product
    Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1048-2024·2024-02-28

    Dover Foley catheter convenience kits recalled due to component defects

    Cardinal Health is recalling Dover-branded Foley catheter convenience kits with components that were subsequently recalled by Nurse Assist. The recall affects 195,600 units distributed in the US, EMEA region, Japan, and Latin America.

    Product
    Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 18 FR (6.0 MM), 5 CC, 2000 ML DRAIN BAG; Dover" HYDROGEL COATED LATEX FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML BAG, D
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0909-2024·2024-02-28

    Hale and Hearty Tomato Basil and Rice Soup Recalled for Undeclared Soy

    Hale and Hearty Soups is recalling Tomato Basil and Rice soup (UPC 635508547872) due to undeclared soy allergen. Consumers with soy allergies should not consume this product.

    Product
    Hale and Hearty Soups; Tomato Basil and Rice; UPC 635508547872
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0333-2024·2024-02-28

    FDA Recalls Neptune's Fix Tianeptine Elixir for Containing Unapproved Drug

    Neptune's Fix Tianeptine Elixir has been recalled because it contains tianeptine, an unapproved drug substance in the United States. Approximately 1 million bottles distributed nationwide are affected.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1079-2024·2024-02-28

    Surgical Kit with Saline Recalled Over Sterility Assurance Issue

    Windstone Medical Packaging is recalling a surgical kit due to inability to guarantee sterility of the included saline. The recall affects 1,528 units distributed in Florida, Illinois, and California.

    Product
    Aligned Medical Solutions, Local Lower Extremity Pack I, AMS10833, STERILEEO
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1049-2024·2024-02-28

    Dover Irrigation Convenience Kits Recalled for Component Defects

    Cardinal Health is recalling Dover Irrigation convenience kits that contained components which were separately recalled. The recall affects over 63,000 units distributed across the US, EMEA, Japan, and Latin America.

    Product
    Dover" IRRIGATION 1200 CC TRAY, 60 CC PISTON SYRINGE, STERILE SALINE, TIP PROTECTOR, ALCOHOL, LIDDED
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0346-2024·2024-02-28

    TING Athlete's Foot Spray Recalled Due to Benzene Contamination

    Insight Pharmaceuticals is recalling TING 1% Tolnaftate Athlete's Foot Spray due to benzene contamination. The recall affects approximately 59,644 cans distributed nationwide.

    Product
    TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1082-2024·2024-02-28

    Medical Closure Kit Recall: Sterility of Saline Cannot Be Guaranteed

    Windstone Medical Packaging is recalling Aligned Medical Solutions Closure Kits due to inability to guarantee sterility of included saline. This FDA Class I recall affects 475 units distributed in Florida, Illinois, and California.

    Product
    Aligned Medical Solutions, Closure Kit, AMS13043, STERILEEO
    Category
    Medical Device
    Distribution
    3 states