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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5026–5050 of 113838

  • CriticalFDA (Devices)·Z-0590-2026·2025-12-17

    Frozen chikoo slices recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen chikoo slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·H-0318-2026·2025-12-17

    Peppermint peaches recalled over potential Listeria monocytogenes contamination

    Moonlight Packing is recalling 570 cases of 2 lb Peppermint Peach bags over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.

    Product
    UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORPORATION REEDLEY, CA 93654
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0295-2026·2025-12-17

    Frozen yellow turmeric haldi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen turmeric haldi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Turmeric Yellow Haldi KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0291-2026·2025-12-17

    Frozen diced bottle gourd recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen diced bottle gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Dudhi (Lauki) Diced Bottle Gourd KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0252-2026·2025-12-17

    ErgoStar CM 40 airway connectors recalled after cracks formed in the hose

    Draeger is recalling 14,420 ErgoStar CM 40 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Chikoo Slices KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0591-2026·2025-12-17

    Ventilator airway connectors recalled after cracks formed in the hose

    Draeger is recalling 191,470 ErgoStar CM 45 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.

    Product
    ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
    Category
    Medical Device
    Distribution
    10 states
  • CriticalFDA (Devices)·Z-0902-2026·2025-12-17

    Frozen baby bhindi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen baby bhindi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·25V871000·2025-12-17

    BMW Recalls 2014-2015 Models Due to Head Air Bag Inflator Defect

    BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.

    Product
    BMW — BMW M235I, 228I, 328I, 320I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V875000·2025-12-17

    Autocar Recalls 2024 E-ACTT Tractor for Battery Cable Fire Risk

    Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V876000·2025-12-17

    Wheelchair restraint retractors in converted vans may fail to lock

    Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.

    Product
    CHRYSLER — CHRYSLER, TOYOTA, DODGE VOYAGER, SIENNA HYBRID, GRAND CARAVAN, PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V872000·2025-12-17

    Toyota Highlander third row seat belt anchor may be installed incorrectly

    Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V873000·2025-12-17

    Suzuki Recalls 2025-2026 DR-Z400 Motorcycles for Brake Fluid Leak Risk

    Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.

    Product
    SUZUKI — SUZUKI DR-Z400S, DR-Z400SM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0284-2026·2025-12-17

    Cinacalcet 60 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 15,744 bottles of Cinacalcet Hydrochloride Tablets, 60 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    Deep-brand PREMIUM Select Mixed Vegetables 4 way KEEP FROZEN a) Net Wt. 3.85 LB. (1.75 kg); b) Net Wt. 2 LB (907 g)
    Category
    Drug
    Distribution
    0 states
  • HighNHTSA·25V874000·2025-12-17

    Kia Sportage instrument panel screen may fail due to software error

    Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.

    Product
    KIA — KIA SPORTAGE, SPORTAGE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0224-2026·2025-12-17

    Cinacalcet 30 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2026·2025-12-17

    Adhesive bandages recalled over open package seals that may compromise sterility

    Medline is recalling 1,566,500 Fur Friends Plastic Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, right, modular, L= 68 mm, Taper 10/12. Knee component of limb salvage replacement devices.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·H-0268-2026·2025-12-17

    Curad Quick Strip fabric bandages recalled over compromised package seals

    Medline is recalling 18,000 units of Curad Quick Strip Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Deep-brand Select Arvi Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0281-2026·2025-12-17

    Quick Strip fabric bandages, 1 by 3 inch, recalled over open seals

    Medline is recalling 11,291,800 Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Deep-brand PREMIUM Select Garlic Cloves Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0597-2026·2025-12-17

    Fluoroscopy systems recalled after shipping without the source-to-skin distance spacer

    Philips is recalling 110 Azurion R3.0 systems shipped with a FlexArm stand but without the Source-to-Skin Distance spacer needed to meet the FDA minimum 38 cm requirement.

    Product
    Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM
    Category
    Medical Device
    Distribution
    0 states