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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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)

12701–12725 of 31488

  • ModerateFDA (Drugs)·D-0595-2024·2024-07-17

    Micafungin injection vials recalled for cross-contamination

    Zydus Pharmaceuticals is recalling Micafungin for injection (100 mg/vial, Lot #L300220) due to potential cross-contamination with other products. Approximately 12,720 vials distributed nationwide in the USA and Puerto Rico are affected.

    Product
    Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1725-01 (vial), NDC 70710-1725-06 (outer box).
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2339-2024·2024-07-17

    Braun Thermoscan PRO 6000 Recall: Outdated Instructions on Included CD

    Braun Thermoscan PRO 6000 ear thermometers may have been shipped with outdated Instructions for Use on an included CD. Approximately 265,647 units were distributed globally.

    Product
    Braun Thermoscan¿ PRO 6000 Ear Thermometer
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0589-2024·2024-07-17

    Suntegrity IMPECCABLE SKIN Sunscreen Foundation Recalled for Manufacturing Deviations

    Suntegrity IMPECCABLE SKIN sunscreen foundation is being recalled due to Current Good Manufacturing Practice (CGMP) deviations. The recall involves 8,202 tubes distributed nationwide and internationally.

    Product
    IMPECCABLE SKIN - IVORY — IMPECCABLE SKIN - IVORY (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V862000·2024-07-12

    2022-2023 Tesla Model S and X Door Latch Safety Defect Recall

    Certain 2022-2023 Tesla Model S and X vehicles may have cabin doors that unlock during a crash due to a door latch defect. Tesla is providing a free over-the-air software update to fix the issue.

    Product
    TESLA — 2022 TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V860000·2024-07-12

    Airstream Basecamp Travel Trailers Recalled for Failing Spare Tire Bracket

    The spare tire carrier bracket on certain 2012-2023 Airstream Basecamp travel trailers may experience metal fatigue and break, causing the spare tire to detach and become a road hazard. Airstream is providing free replacement and reinforcement of the bracket.

    Product
    AIRSTREAM — 2023 AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24302·2024-07-11

    Best Lighting Products LED High Bay Light Fixtures Recalled for Fire Hazard

    Best Lighting Products is recalling approximately 710,600 LED High Bay Light Fixtures because plastic pins securing the LED board can degrade, allowing the energized board to come loose and pose a fire hazard. Three fires have been reported.

    Product
    LED High Bay Light Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24303·2024-07-11

    TonGass Pool Drain Covers Recalled for Entrapment Hazard

    TonGass 8-inch round pool drain covers do not meet Virginia Graeme Baker Pool and Spa Safety Act standards and pose an entrapment hazard to swimmers and bathers. About 1,650 units sold on Amazon from September 2023 through June 2024 are affected.

    Product
    TonGass pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24301·2024-07-11

    Children's Pajama Sets Recalled for Burn Hazard and Flammability Violation

    JUVENNO KIDS is recalling about 18,620 children's button-up pajama sets sold on Temu.com because they violate federal flammability standards for sleepwear and pose a burn injury risk to children. No injuries have been reported.

    Product
    Children's Button-up Short-Sleeve/Shorts Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24300·2024-07-11

    Children's Lace Nightgowns Recalled for Burn Hazard

    Lovely Angel children's lace nightgowns sold on Temu.com violate federal flammability standards for sleepwear, posing a burn injury risk to children. About 4,360 units were sold between June 2023 and May 2024.

    Product
    Lovely Angel Children's Lace Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V839000·2024-07-11

    2022-2023 Chevrolet Express and GMC Savana transmission software defect

    GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.

    Product
    GMC — 2023 GMC SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24298·2024-07-11

    Atomi Smart Heaters recalled for fire and burn hazards

    Atomi Smart Heaters can turn on without user input, creating fire and burn risks. About 99,400 units sold nationwide are affected; consumers should stop use immediately and follow refund instructions.

    Product
    Atomi Smart Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V843000·2024-07-11

    2024 Hyundai Santa Fe sunshade switch defect increases injury risk

    Hyundai is recalling 34,964 units of the 2024 Santa Fe and Santa Fe Hybrid with faulty switch knobs that may not retract, creating an injury risk.

    Product
    HYUNDAI — 2024 HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24299·2024-07-11

    Claire's and Icing Stores Halloween Witch Hats Burn Hazard Recall

    Claire's and Icing stores are recalling about 5,700 Halloween witch hats sold nationwide from July through December 2023. The hats violate federal flammability requirements and pose a risk of burn injuries.

    Product
    Halloween Witch Hats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24296·2024-07-11

    Children's Pajama Sets Recalled for Flammability Hazard

    About 45,300 children's two-piece pajama sets sold on Temu.com violate federal flammability standards for sleepwear, posing a burn risk to children. Consumers should immediately stop using the garments and contact Fashion Online for a refund.

    Product
    Children's Long-Sleeve/Pants Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24297·2024-07-11

    Metal-framed Armchairs Recalled for Fall and Injury Hazards

    Ross Stores is recalling about 1,600 metal-framed armchairs because the chair legs can bend or break, posing fall and injury hazards. The company has received five reports of broken legs, four of which resulted in minor injuries.

    Product
    Metal-framed Armchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0585-2024·2024-07-10

    RAM IT Horny Goat Weed Dietary Supplement Recalled for Undeclared Sildenafil

    Integrity Products recalls RAM IT Horny Goat Weed dietary supplement capsules nationwide because they contain undeclared sildenafil, a prescription drug not listed on the label.

    Product
    RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0586-2024·2024-07-10

    Horny Goat Weed Capsules Recalled for Undeclared Sildenafil

    To the Moon Capsules are being recalled nationwide because they contain undeclared sildenafil, a prescription pharmaceutical. The product was marketed without FDA approval.

    Product
    To the Moon Capsules, Horny Goat Weed, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2024·2024-07-10

    Megadyne MEGA 2000 Patient Return Electrode recalled for burn risk

    Megadyne is recalling the MEGA 2000 Patient Return Electrode due to identified potential risk of patient burns. Use is now restricted to patients aged 12 or older.

    Product
    Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode Model/Catalog Number: 0800 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega 2000, Adult, For Patients Weighing over 25lbs. (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1432-2024·2024-07-10

    Thyroid Supplement Recalled for Potential Salmonella Contamination

    Penn Herb Company is recalling Nature's Wonderland brand Thyroid Formula due to potential Salmonella contamination. Fifty-one bottles were distributed across nine states.

    Product
    Nature's Wonderland brand Thyroid Formula 60 Veg Capsules UPC: 715486893205. Packaged in White PET 150cc bottle with security closure
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·22V816000·2024-07-10

    2021 Hyundai Santa Fe Hybrid seat belt pretensioners may explode in crash

    Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.

    Product
    HYUNDAI — 2021 HYUNDAI SANTA FE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2250-2024·2024-07-10

    Reusable Patient Return Electrode Recalled Due to Burn Risk

    MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrodes are recalled due to an identified risk of patient burns. Use should be restricted to patients aged 12 or older.

    Product
    Brand Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Model/Catalog Number: 0835 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Dual Cord, Adu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2249-2024·2024-07-10

    MEGADYNE MEGA SOFT Reusable Patient Return Electrode Recalled for Burn Risk

    Megadyne Medical recalls MEGA SOFT reusable patient return electrodes (Model 0830) due to identified burn risk. Use is restricted to patients aged 12 and older.

    Product
    Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Model/Catalog Number: 0830 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Single Cord, Adult, For
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2227-2024·2024-07-10

    Medline Birthing Room Pack surgical kits recalled due to weak sterile seals

    Medline is recalling approximately 12,588 sterile surgical kits used for childbirth procedures because weak seals on Pure Pouch components may fail and compromise sterility.

    Product
    Sterile convenience kit: Medline Birthing Room Pack, Pack #DYNJ38429D, containing a Pure Pouch component Sterile Sharp/Blunt Scissors 5.5", Reorder #65945 and containing a Pure Pouch component Sterile 5.5" Episiotomy Scissors, Reorder #67645.
    Category
    Medical Device
    Distribution
    Distributed nationwide