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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

16476–16500 of 31567

  • ModerateFDA (Drugs)·D-0140-2024·2023-12-13

    LET Gel Topical Anesthetic Recalled Due to Incorrect Product Formulation

    Right Value Drug Stores is recalling LET Gel topical anesthetic syringes nationwide due to incorrect product formulation. Patients should not use affected syringes and should consult their healthcare provider.

    Product
    LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), Single-use Topical Syringe, 3mL syringe, 10/pack, Rx only, Carie Boyd Pharmaceuticals, 8400 Esters Blvd, Ste# 190, Irving, TX 75063, NDC73271-1003-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0470-2024·2023-12-13

    Intraocular Lens Devices May Not Meet Manufacturing Specifications

    Staar Surgical is recalling 3 units of its EVO+VISIAN Implantable Collamer Lens (phakic toric) due to a potential that devices may not meet specifications. No illnesses or injuries have been reported.

    Product
    EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_12.1. Phakic Toric Intraocular lens.
    Category
    Medical Device
    Distribution
    38 states
  • ModerateFDA (Devices)·Z-0479-2024·2023-12-13

    HeartWare HVAD Implant Kit Instructional Update for Fault Alarms

    The FDA is issuing updated instructions for the HeartWare HVAD ventricular assist device to clarify when controller fault alarms sound and when device components should be replaced. No patient harm has been reported.

    Product
    PUMP 1104 HVAD (HeartWare Ventricular Assist Device) IMPLANT KIT, Model Number 1104
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0506-2024·2023-12-13

    TENS Devices Recalled for Missing Instruction Manual Warnings

    Liberty Medical Solutions is recalling 473 Multi-Mode TENS stimulator units distributed in five states due to missing warnings and contraindications in instruction manuals.

    Product
    Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0137-2024·2023-12-13

    Bupropion Hydrochloride Extended-Release Tablets Recalled for Failed Dissolution

    Sun Pharmaceutical is recalling Bupropion Hydrochloride Extended-Release Tablets 200 mg due to failed dissolution specifications. The recall affects 2,016 bottles with lot HAD0630A distributed nationwide.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0451-2024·2023-12-13

    Blood Culture Identification Panel Quality Control Test Reporting Issue

    BioFire Diagnostics is recalling BIOFIRE Blood Culture Identification 2 (BCID2) Panels due to instrument characteristic changes that cause Candida tropicalis to be detected but reported as 'Not Detected' in quality control testing.

    Product
    BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls, Inc (MMQCI) FilmArray BCID2 Control Panel M416, which is referenced in Quality Control Materials for use with BIOFIRE FILMARRAY and BIOFIRE SPOTFIRE Panels - FLM1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0469-2024·2023-12-13

    EVO VISIAN Intraocular Lens Recalled Due to Specification Concerns

    Staar Surgical Company is recalling EVO VISIAN Implantable Collamer Lens devices due to potential specification defects. Two units distributed across the United States are affected.

    Product
    EVO VISIAN Implantable Collamer Lens REF: VICMO13.2. Phakic Intraocular lens.
    Category
    Medical Device
    Distribution
    38 states
  • ModerateFDA (Devices)·Z-0500-2024·2023-12-13

    Luminex VERIGENE BC-GP Utility Trays Recalled Due to Potential Defects

    Luminex Corporation is recalling 222 kits (4,440 VERIGENE BC-GP Utility Trays) used in blood culture testing due to potentially defective utility trays. The affected lot (062123018C) expires December 20, 2023.

    Product
    Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier), Gram-Positive Blood Culture Nucleic Acid Test, REF 20-011-018, a component of the Luminex VERIGENE BC-GP Utility Kit, REF 20-012-018, containing 20 tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0486-2024·2023-12-13

    Almond and pistachio fudge recalled for undeclared color additives

    BAPS Shayona is recalling Badam Pista Sandwich due to undeclared Yellow #5 and Green 3 color additives. The product was distributed to six states.

    Product
    BAPS SHAYONA Badam Pista Sandwich Almond and pistachio layered fudge Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53009 Contains: Nuts
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0494-2024·2023-12-13

    BAPS Shayona Motichur Ladoo recalled for undeclared Yellow #5 and Yellow #6 dyes

    BAPS Shayona is recalling approximately 674 units of Motichur Ladoo across six states due to undeclared Yellow #5 and Yellow #6 food dyes discovered during an FDA inspection.

    Product
    BAPS SHAYONA Motichur Ladoo Sweet chickpea flour mini-pearls rolled into spheres Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53160 Contains: Milk
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0475-2024·2023-12-13

    HVAD Ventricular Assist Device Instructions Updated for Alarm Clarification

    Heartware, Inc. is updating instructions for the HVAD ventricular assist device to clarify Controller Fault alarm conditions and component useful life. The recall affects 45 units distributed worldwide.

    Product
    HVAD (HeartWare Ventricular Assist Device) STERILE IMPLANT KIT, Model Number 1100
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0481-2024·2023-12-13

    Ventricular Assist Device Instructions Updated for Alarm and Useful Life Clarification

    Heartware is updating instructions for HVAD ventricular assist device implant kits to clarify Controller Fault alarm conditions and troubleshooting steps, as well as useful life information for system components.

    Product
    PUMP 1104 HVAD (HeartWare Ventricular Assist Device) IMPLANT KIT EN JA, Model Number 1104JP
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0487-2024·2023-12-13

    Remington Medical drainage bags recalled due to packaging label date error

    Remington Medical is recalling drainage bags (Lot 2325111) due to errors in the 'Use by Date' and 'Date of Manufacturer' on box labels. Approximately 3,080 units distributed in PA and FL are affected.

    Product
    Remington MEDICAL Drainage Bag, REF 600-D;
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0488-2024·2023-12-13

    Vyaire Flexible Patient Circuit 3100A Distributed Without U.S. Approval

    Vyaire Medical recalled 188 Flexible Patient Circuit 3100A units distributed in Florida that were approved only for use outside the United States. The circuits were mistakenly distributed in the U.S. market.

    Product
    vyaire Flexible Patient Circuit, 3100A, REF 29028-003, intended to be used with the 3100A High Frequency Oscillatory Ventilator (HFOV)
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·23V838000·2023-12-12

    Tesla Model Y Autosteer Recall: Software Update for Control Prominence

    Tesla is recalling 2.03 million 2012-2023 Model S/X/3/Y vehicles with Autosteer due to insufficient control prominence that may allow driver misuse and crash risk. A free OTA software update will be provided.

    Product
    TESLA — 2022 TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V680000·2023-12-10

    2023 Toyota 4Runner Load Capacity Label Correction Recall

    Southeast Toyota Distributors is recalling certain 2023 Toyota 4Runner vehicles due to an incorrect load carrying capacity modification label. The error could result in vehicle overloading and increased crash risk.

    Product
    TOYOTA — 2023 TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V681000·2023-12-10

    GMC Acadia and Cadillac Windshield Detachment Risk Recall

    General Motors is recalling 2023 GMC Acadia vehicles and certain 2024 Cadillac models due to windshields that may not be properly bonded to the vehicle body. A detached windshield during a crash could increase the risk of injury.

    Product
    GMC — 2023 GMC ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V682000·2023-12-10

    2023 Cadillac Lyriq Pedestrian Warning Sounds May Not Activate

    General Motors is recalling certain 2023 Cadillac Lyriq vehicles due to a software defect in the body control module. The pedestrian warning sounds may fail to activate, creating a crash risk.

    Product
    CADILLAC — 2023 CADILLAC LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24048·2023-12-07

    XpressGoods recalls magnetic balls for federal toy safety violations

    XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Colorful Metal Neodymium Magic Magnetic Balls - 8 color, 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24727·2023-12-07

    2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles Fire Hazard Recall

    Segway Powersports is recalling about 1,100 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles because the ignition coil can fail, allowing fuel to enter the exhaust pipe and ignite, creating a fire hazard. One vehicle fire with property damage has been reported.

    Product
    2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V477000·2023-12-07

    Jayco Seneca recreational vehicles recalled for windshield wiper linkage failure

    Jayco is recalling certain 2021-2022 Seneca recreational vehicles because the windshield wiper arms may fail, reducing driver visibility and increasing crash risk. Owners should contact Jayco customer service at 1-800-283-8267 for a free inspection and replacement.

    Product
    JAYCO — 2021 JAYCO SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24043·2023-12-07

    Wet & Forget Xtreme Reach Stain Remover with Hose End Nozzle Recalled

    Wet & Forget USA is recalling about 2.7 million bottles of "Xtreme Reach" Outdoor Mold & Mildew Stain Remover with hose end nozzles. The nozzle clip can dislodge, spraying cleaning solution on users and causing skin and eye irritation.

    Product
    Wet & Forget "Xtreme Reach" Outdoor Rapid Application Moss, Mold, Mildew & Algae Stain Remover with Hose End Nozzle
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V476000·2023-12-07

    Polestar 2 Recalled for Potential Steering Loss Due to Defective Ball Joint

    Polestar is recalling certain 2023 Polestar 2 vehicles due to a defect in the front left lower ball joint that could cause loss of steering control. Owners should contact their dealer for a free inspection and replacement.

    Product
    POLESTAR — 2023 POLESTAR POLESTAR 2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24041·2023-12-07

    Nap Queen Maxima Hybrid Mattresses Recalled for Fire Hazard

    Adven Group LLC is recalling about 1,540 Nap Queen 12-inch Maxima Hybrid Mattresses sold via Amazon, Walmart, and Overstock because they fail to meet federal flammability standards and pose a fire hazard.

    Product
    Nap Queen 12-inch Maxima Hybrid Mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide