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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8051–8075 of 114917

  • ModerateFDA (Devices)·Z-2579-2025·2025-09-24

    Fourteen millimetre distraction pins recalled over unvalidated shelf life labeling

    Frontier Devices 14 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 10,960 units are affected.

    Product
    Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 10 single packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0594-2025·2025-09-24

    Quercetin tablets recalled over unapproved drug claims and misbranding on label

    Hi-Tech Pharmaceuticals Quercetin, 120 tablets, lot C1612, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CARDIOVASCULAR HEALTH 120 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02491 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0590-2025·2025-09-24

    Joint supplement recalled over unapproved drug claims on the label

    Hi-Tech Pharmaceuticals Joint-RX dietary supplement, 90 count, lot 503110607, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity Dr Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2585-2025·2025-09-24

    Blood gas EG6+ cartridges recalled for lacking updated premarket clearance

    i-STAT EG6+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 547,250 units are affected.

    Product
    i-STAT EG6+ cartridge. List Number: 03P77-25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2584-2025·2025-09-24

    Blood gas EG7+ cartridges recalled for lacking updated premarket clearance

    i-STAT EG7+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 6,115,950 units are affected.

    Product
    i-STAT EG7+ cartridge. List Number: 03P76-25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2560-2025·2025-09-24

    Lactate slides in 18-slide cartridges recalled over calibration failures delaying results

    VITROS Chemistry Products LAC Slides, catalog 8150112, from coating 0130 and above are recalled because of increased calibration failures on VITROS XT systems, delaying lactate results. 2,320 units are affected.

    Product
    VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slides, for a total of 90 tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0598-2025·2025-09-24

    Taurine powder recalled over unapproved drug claims and misbranding

    PrimeNutrition Taurine, 8.12 oz, lot 710581618, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS ENERGY PRODUCTION PROTEN ANTIOXIDANT PROPERTIES SUPPORTS HEALTHY BLOOD SUGAR LEVELS NET WT. 8.12OZ (250g) DIETARY SUPPLEMENT UPC 6 89466 70601 7 Manufactured by: Prime Nutrition 6015-B Unity Drive…
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2582-2025·2025-09-24

    Blood gas cartridges recalled for lacking clearance covering updated measurement ranges

    i-STAT CG4+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting the updated lactate sample type and pH and PO2 measurement ranges. 9,067,050 units are affected.

    Product
    i-STAT CG4+ cartridge (white). List Number: 03P85-25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2577-2025·2025-09-24

    Twelve millimetre distraction pins recalled over unvalidated shelf life labeling

    Frontier Devices 12 mm Distraction Pins in 10 double packs are recalled because the labeling includes a shelf life that has not been validated. 160 units are affected.

    Product
    Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2025·2025-09-24

    Distraction pins in double packs recalled over unvalidated shelf life labeling

    Frontier Devices 14 mm Distraction Pins in 10 double packs are recalled because the labeling includes a shelf life that has not been validated.

    Product
    Frontier Devices, REF: 301.914S2, 14 mm Distraction Pin, 10 double packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2576-2025·2025-09-24

    Distraction pins in single packs recalled over shelf life that was not validated

    Frontier Devices 12 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 3,790 units are affected.

    Product
    Frontier Devices, REF: 301.912S1, 12 mm Distraction Pin, 10 single packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V635000·2025-09-23

    Blue Bird Recalls Vision Buses Due to Brake Software Defect

    Blue Bird is recalling 2021-2026 Vision school and transit buses because brake software may activate the parking brake unexpectedly, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V636000·2025-09-23

    BMW and Toyota Supra starter relays can corrode and short circuit

    BMW is recalling certain 2019-2022 BMW models and the Toyota Supra because the engine starter relay may corrode, overheat and short circuit. Owners are told to park outside until repaired.

    Product
    BMW — BMW, TOYOTA 230I, 530I, SUPRA, Z4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V634000·2025-09-23

    Porsche Cayenne, Panamera fuel pump fasteners inadequately tightened

    Porsche is recalling certain 2024–2026 Cayenne and Panamera models because fasteners securing the high pressure fuel pump may not be tightened properly, creating a fuel leak risk and potential fire hazard.

    Product
    PORSCHE — PORSCHE CAYENNE, PANAMERA 4 E-HYBRID, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V632000·2025-09-19

    MCI Recalls 2024-2025 Electric Coaches Due to Battery Fire Risk

    Motor Coach Industries is recalling specific 2024 and 2025 electric coaches because a high-voltage battery short circuit could cause a fire.

    Product
    MCI — MCI D45CRTELE, J4500E, D45CRTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V626000·2025-09-19

    Ford Super Duty steering column upper shaft can detach

    Ford is recalling certain 2020-2021 F-250, F-350 and F-450 vehicles because the steering column upper shaft may detach from the steering column, causing a loss of steering control.

    Product
    FORD — FORD F-350 SD, F-250 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V628000·2025-09-19

    Ford Recalls 2020 Expedition and Lincoln Navigator for Fire Risk

    Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a short circuit in the battery junction box can cause an engine fire.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V630000·2025-09-19

    Isuzu and Chevrolet truck fuel heaters can overheat and leak fuel

    Isuzu is recalling certain 2022-2026 FVR, FTR and Chevrolet 6500XD and 7500XD vehicles because the fuel heater may overheat, melting the casing and allowing fuel to leak into the electrical connector.

    Product
    CHEVROLET — CHEVROLET, ISUZU 7500XD, 6500XD, FVR, FTR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V631000·2025-09-19

    New Flyer Recalls Transit Buses Due to High Voltage Battery Fire Risk

    New Flyer is recalling 2019-2025 XE35, XE40, and XE60 transit buses because a high voltage battery short circuit may cause a fire. Owners should park outside and limit charging to 75%.

    Product
    NEW FLYER — NEW FLYER XE35, XE60, XE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09192025-01·2025-09-19

    USDA Issues Public Health Alert for Trader Joe's Turkey Wrap Due to Listeria

    USDA FSIS issued a public health alert for Trader Joe's Turkey Gobbler Wraps produced on September 10, 2025, due to possible Listeria monocytogenes contamination.

    Product
    WCD Kitchen - Minooka — FSIS Issues Public Health Alert for Ready-To-Eat Turkey Wrap Product Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V629000·2025-09-19

    Altec certification labels may list an incorrect axle weight rating

    Altec is recalling certain 2022-2025 Aerial Device, Forestry Body, Service Body and Digger Derrick vehicles because the Gross Axle Weight Rating on the certification label may be incorrect.

    Product
    ALTEC — ALTEC FORESTRY BODY, AERIAL DEVICE, DIGGER DERRICK, SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25469·2025-09-18

    Cotton candy makers recalled after twelve reports of sparking or fire

    About 21,690 Ambiano cotton candy makers, model 836098, are recalled because the heating element can ignite sugar if used without the sugar receptacle. Twelve sparking or fire reports; no injuries.

    Product
    Ambiano Cotton Candy Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide