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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8076–8100 of 31207

  • HighFDA (Drugs)·D-0306-2025·2025-04-09

    Biocon Pharma atorvastatin calcium tablets recalled for failed dissolution specifications

    Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2025·2025-04-09

    BD Connecta Stopcocks Recalled for Non-U.S. Instructions Shipped to U.S. Market

    BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.

    Product
    BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-1486-2025·2025-04-09

    GE Healthcare Cardiology CA1000 Security Vulnerability Could Allow Patient Data Access

    GE Healthcare Centricity Cardiology CA1000 has a security vulnerability where service login credentials can be identified, potentially allowing unauthorized access to patient data.

    Product
    GE Healthcare Centricity Cardiology CA1000 (CA1000), Model Numbers: 1) 2033901-001; 2) 2038437-001; 3) 2038437-009; 4) 2038437-014; 5) 2038437-015 ; 6) 2038437-0XX; 7) 2109571-007; 8) 2109571-010; 9) 2109571-011; 10) 2109571-012; 11) MANLEGACY111; 12) MAN
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·25V580000·2025-04-09

    IC Bus School Buses Recalled for Structural Reinforcement Defect

    International Motors is recalling certain 2016-2026 IC Bus CESB and 2016-2021 RESB school buses due to missing or incomplete underfloor reinforcement that may compromise crash safety. Owners should contact a dealer for free inspection and installation.

    Product
    IC BUS — 2020 IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0307-2025·2025-04-09

    Voriconazole Tablets Recalled Due to Manufacturing Practice Deviations

    Amerisource Health Services is recalling Voriconazole 50 mg tablets distributed nationwide due to current Good Manufacturing Practice deviations related to repackaging.

    Product
    VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1503-2025·2025-04-09

    Laboratory diagnostic reagent distributed with incorrect calibration value on package label

    Fisher Diagnostics is recalling Pacific Hemostasis Thromboplastin-D reagent (1,699 units) due to an incorrect International Sensitivity Index (ISI) value printed on the box. No illnesses or injuries have been reported.

    Product
    Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0305-2025·2025-04-09

    Sterile ophthalmic solution recalled for subpotent drug strength

    Imprimis NJOF is recalling 2,822 bottles of sterile ophthalmic solution because stability testing showed subpotent drug strength below specifications.

    Product
    Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5 mL fill in 15 mL bottle, Imprimis NJOF, LLC, Route 46 West, Unit 6B, Ledgewood, NJ, 07852, NDC: 71384-733-05.
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0309-2025·2025-04-09

    Prescription Antipsychotic Drug Recalled for Manufacturing Impurity

    Glenmark Pharmaceuticals is recalling Chlorpromazine Hydrochloride Tablets due to a manufacturing quality deviation involving an impurity above recommended limits.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0304-2025·2025-04-09

    Tolterodine Tartrate Extended-Release Capsules Recalled for Failed Dissolution

    Tolterodine Tartrate Extended-Release Capsules, 2 mg (Lot T05393) are being recalled because they failed dissolution specifications. The capsules may not dissolve as intended.

    Product
    TOLTERODINE TARTRATE — TOLTERODINE TARTRATE (TOLTERODINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1513-2025·2025-04-09

    Surgical Suture Needles Recalled Due to Manufacturing Defect

    Ethicon Endo Surgery recalls PDS PLUS VIO surgical sutures with needles due to silicone curing defects during manufacturing. 792 units were distributed worldwide.

    Product
    PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V499000·2025-04-08

    2024-2025 Winnebago Ekko RV Tire Valve Extension Defect Recall

    Winnebago is recalling certain 2024-2025 Ekko recreational vehicles due to damaged tire valve extensions that can cause air loss in the inner tire and overload the outer tire, creating a crash risk. Dealers will replace the extensions free of charge.

    Product
    WINNEBAGO — 2024 WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V533000·2025-04-07

    2024 Porsche Cayenne Front Suspension Control Arm May Crack and Fail

    Porsche is recalling 2,475 2024 Cayenne vehicles due to potentially cracked driver's side front upper control arms that may break and cause loss of steering control.

    Product
    PORSCHE — 2024 PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V452000·2025-04-06

    Certain 2021–2025 Lion LionC School Buses Electrical Hardware Recall

    Lion Electric is recalling 2021–2025 LionC school buses due to loose electrical hardware that could cause short circuits and loss of steering or braking power. Contact Lion customer service at 1-855-546-6706 for free replacement.

    Product
    LION — 2021 LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V336000·2025-04-06

    Mazda MX-5 recalled for Dynamic Stability Control indicator light failure

    Mazda is recalling 2024-2025 MX-5 vehicles where the Dynamic Stability Control indicator light may fail to illuminate due to a software error. This could prevent drivers from being warned of a traction control system failure, increasing crash risk.

    Product
    MAZDA — 2025 MAZDA MX-5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V449000·2025-04-06

    2022-2023 BMW I4 Recalled for High Voltage Battery Charging Unit Failure

    BMW recalls certain 2022-2023 I4, iX, and i760 models due to a defective high voltage battery charging unit that may not have been properly assembled, potentially causing engine stall while driving.

    Product
    BMW — 2022 BMW I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V324000·2025-04-06

    2025 Nissan Frontier rear display may blank in reverse

    The 2025 Nissan Frontier's center information display may show a blank screen in reverse, violating federal rear-visibility standards. This could reduce driver visibility and increase crash risk.

    Product
    NISSAN — 2025 NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V346000·2025-04-05

    2024 Jeep Grand Cherokee: Missing Bumper Foam May Prevent Airbag Deployment

    Certain 2024 Jeep Grand Cherokees may be missing foam in the front bumper, which could prevent the front airbags from deploying during a crash. Dealers will install the foam at no cost.

    Product
    JEEP — 2024 JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V348000·2025-04-05

    2024 Lamborghini Urus Hood Latch May Separate While Driving

    Lamborghini is recalling 2023-2024 Urus Performante and Urus S vehicles because the hood latch striker may separate, causing the hood to open or detach while driving and create a road hazard.

    Product
    LAMBORGHINI — 2024 LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V271000·2025-04-04

    2023 Kia Niro EV Differential Bolt Recall: Loss of Drive Power Risk

    Kia is recalling certain 2023 Niro EV vehicles because differential gear bolts may not be properly tightened, potentially causing loss of drive power or differential lock-up, which can increase crash risk.

    Product
    KIA — 2023 KIA NIRO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V307000·2025-04-04

    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 — 2023 WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V305000·2025-04-04

    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 — 2020 FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25208·2025-04-03

    Polaris RZR Pro R and Pro R 4 recalled for ROPS fastener defect

    Polaris is recalling about 910 RZR Pro R and Pro R 4 recreational off-road vehicles (2022-2025) due to missing or loose fasteners on the rollover protective structure that can fail to protect occupants in a rollover or tip-over.

    Product
    Model Year 2022-2025 RZR Pro R and RZR Pro R 4 Recreational Off-Road Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25204·2025-04-03

    USB-Powered LED Bear Lights Recalled for Fire and Burn Hazards

    Five Below is recalling about 29,000 LED Iridescent Bear Lights because the USB power switch can overheat and melt. The company received 28 reports of overheating, including 6 finger burns and 2 property damage incidents.

    Product
    Room2Room LED Iridescent Bear Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25207·2025-04-03

    Honda Recalls Accessory Heaters for Side-by-Side Vehicles Due to Fire Hazards

    Honda is recalling about 2,340 aftermarket accessory heaters for Pioneer and Talon side-by-side vehicles because they can overheat and catch fire. The company has received three reports of overheating, including two that resulted in fires and vehicle damage.

    Product
    Accessory Heaters for Model Years 2022-2024 Honda Pioneer 1000, 2023-2025 Pioneer 700, and 2022-2024 Honda Talon 1000 Side-by-Side vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide