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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3226–3250 of 36538

  • SevereFDA (Devices)·Z-0298-2025·2024-11-20

    FDA Updates POLARx Cryoablation Catheter Instructions for Atrio-esophageal Fistula Risk

    Boston Scientific is updating instructions for POLARx and POLARx FIT cryoablation catheters to address atrio-esophageal fistula risks. The FDA classified this as a Class I recall affecting approximately 20,290 units distributed worldwide.

    Product
    Boston Scientific POLARx BALLOON CATHETER LT 28MM OUS, Material Number M004CRBS2100
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0305-2025·2024-11-20

    Anesthesia workstation piston ventilator may fail before or during use

    Draeger Medical is recalling Atlan A350XL anesthesia workstations due to potential piston ventilator failure that may occur before use or during mechanical ventilation.

    Product
    Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V877000·2024-11-20

    Hyundai Tucson console wiring may allow shifting out of Park unbraked

    Hyundai is recalling certain 2025 Tucson and Santa Cruz vehicles because misrouted console wiring may allow the transmission to shift out of Park without the brake applied.

    Product
    HYUNDAI — HYUNDAI SANTA CRUZ, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E099000·2024-11-20

    Agility Fuel Solutions Recalls CNG Fuel Systems Due to Valve Cracks

    Agility Fuel Solutions is recalling certain CNG fuel systems because manual cylinder valves may develop stress corrosion cracks, causing a natural gas leak that increases fire risk.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E098000·2024-11-20

    Lippert Recalls Fifth Wheel Pin Boxes Due to Fastener Issues

    Lippert is recalling specific Curt Helux Pin Boxes installed in Lippert 5W Chassis because fasteners may be improperly tightened, increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0301-2025·2024-11-20

    Boston Scientific Cryoablation Balloon Catheters Instruction Update for Fistula Risk

    Boston Scientific is updating safety instructions for POLARx cryoablation balloon catheters due to atrio-esophageal fistula risk. The update affects approximately 2,751 units distributed worldwide.

    Product
    Boston Scientific POLARx FIT BALLOON CATHETER LT OUS, Material Number M004CRBS2110
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0290-2025·2024-11-20

    Trilogy Evo O2 Ventilators Recalled for Potential Flow Sensor Malfunction

    Philips Respironics recalled 24,249 Trilogy Evo O2 ventilators because in-line nebulizer configurations may allow aerosol deposits to accumulate on the device's flow sensor, potentially causing inaccurate flow measurements.

    Product
    Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, EE2100X15B, FX2100X15B, ES2100X15B, ND2100X15B, FR2100X14B, IT2100X21B, JP2100X16B, IN2100X19, EU2100X19. Intended for invasive and non-invasive ventilation of pedi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0302-2025·2024-11-20

    Boston Scientific Cryoablation Balloon Catheters Recalled for Fistula Risk

    Boston Scientific is updating instructions for POLARx and POLARx FIT cryoablation balloon catheters due to atrio-esophageal fistula risk. Affected devices were distributed worldwide.

    Product
    Boston Scientific POLARx FIT BALLOON CATHETER LT US, Material Number M004CRBS2160
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0291-2025·2024-11-20

    Philips Trilogy Evo ventilators recall: flow sensor fouling risk

    Philips Respironics is recalling Trilogy Evo ventilators due to potential aerosol deposits on the internal flow sensor, which could cause inaccurate flow measurements during ventilation.

    Product
    Trilogy Evo. Model Numbers: DS2110X11B, UDS2110X11B, RDS2110X11B, CA2110X12B, JP2110X16B, IN2110X15B, DE2110X13B, AU2110X15B, BL2110X15B, EU2110X15B, BR2110X18B, LA2110X15B, EE2110X15B, FR2110X14B, GB2110X15B, ND2110X15B, ES2110X15B, IA2110X15B, IT2110X21B, KR2110X15B, TR2110X15B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0297-2025·2024-11-20

    Boston Scientific POLARx Cryoablation Catheters Instructions Updated for Fistula Risk

    Boston Scientific is updating instructions for POLARx and POLARx FIT cryoablation catheters to address atrio-esophageal fistula risk, a potentially serious complication from ablation procedures. FDA Class I recall affecting 4422 units worldwide.

    Product
    Boston Scientific POLARx BALLOON CATHETER ST 28MM OUS, Material Number M004CRBS2000.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0137-2025·2024-11-20

    Yellow Onion Products Recalled for E. Coli O157:H7 Contamination

    IMPERIALFRESH processed yellow onions are being recalled due to potential E. coli O157:H7 contamination. Products were distributed in Colorado and produced October 8-22, 2024.

    Product
    Item Number PACK/SZ BRAND DESCRIPTION Lot Codes 082076 4/5 LBS IMPERIALFRESH PROC ONION YELLOW JULIENNE 3/8 All lot codes; 170992 4/5 LB IMPERIALFRESH PROC ONION YELLOW DICED 3/8 All lot codes; 258147 4/5LBS IMPERIALFRESH PROC ONION YELLOW JULIENNE 1/4 All lot codes; 259369 1 / 5
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0134-2025·2024-11-20

    Raw Yellow Onions Recalled for Potential E. coli O157:H7 Contamination

    Taylor Farms Colorado is recalling 615 cases of raw yellow onions for potential E. coli O157:H7 contamination. Affected food service facilities are in CO, KS, MO, NE, NM, and UT.

    Product
    raw, yellow onions (whole peeled), intended for food service, packaged into plastic bags (5-lbs)
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0133-2025·2024-11-20

    Raw yellow onions recalled for potential E. coli O157:H7 contamination

    Taylor Farms Colorado is recalling raw yellow onions distributed to food service facilities in six states due to potential E. coli O157:H7 contamination. Use-through dates range from October 16 to November 3, 2024.

    Product
    raw, yellow onions (sliced, diced, slivered, ringed), intended for food service, packaged in plastic bags
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0138-2025·2024-11-20

    Processed Fajita Peppers Recalled for Potential E. coli O157:H7 Contamination

    ImperialFresh processed fajita peppers made by FreshPoint Denver, Incorporated have been recalled due to potential E. coli O157:H7 contamination. Seven cases distributed in Colorado are affected.

    Product
    154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W All lot codes
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0312-2025·2024-11-20

    FHC microTargeting Insertion Tube Set Recalled for Spacer Defect

    FHC, Inc. recalls microTargeting Insertion Tube Set Lot 244517, affecting 40 units distributed domestically. The oversized spacer tube component risks intracranial hemorrhaging during neurosurgical procedures.

    Product
    microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended use is to accurately guide a microelectrode or instrument in the brain during stereotactic functional neurosurgical procedures.
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0292-2025·2024-11-20

    Trilogy Evo Universal Ventilator Recalled Due to Sensor Malfunction Risk

    Trilogy Evo Universal Ventilators (Model DS2000X11B) are recalled because in-line nebulizer configuration in certain locations could cause aerosol accumulation on the internal flow sensor, potentially resulting in inaccurate measurements.

    Product
    Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0357-2025·2024-11-20

    Medline Recalls Non-Sterile Urinalysis Kit Specimen Containers

    Medline Industries is recalling 626,305 urinalysis kits because the specimen containers are labeled sterile but are non-sterile, posing a risk of unnecessary treatment or hospitalization.

    Product
    URINALYSIS KIT 4, SKU DYLAB1021; Component No. 503581
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0404-2025·2024-11-20

    AVID Medical Recalls Halyard Laparoscopy Trays Due to Metal Flakes

    AVID Medical is recalling 42 Halyard Laparoscopy Trays because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.

    Product
    Halyard LAPAROSCOPY TRAY - Medical convenience kits Model Number: LANC006-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0406-2025·2024-11-20

    AVID Medical Recalls Halyard C Section Bundles Due to Metal Flakes

    AVID Medical, Inc. is recalling Halyard C Section Bundles because small metal flakes may detach from sponge forceps and towel clamps, posing a risk of foreign body reactions.

    Product
    Halyard C SECTION BUNDLE - Medical convenience kits Model Number: LANC015-34
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V874000·2024-11-19

    Mercedes-Benz Recalls Vehicles Due to Sunroof Detachment Risk

    Mercedes-Benz is recalling 33,456 vehicles because the glass sunroof panel may not be properly secured and can detach, creating a road hazard.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ CLK320, C320, C280, C240
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V870000·2024-11-19

    BMW Recalls 2025 530i and 540i xDrive for Air Bag Control Unit Defect

    BMW is recalling 2025 530i and 540i xDrive vehicles because the air bag control unit may be manufactured incorrectly, potentially preventing air bags from deploying as intended.

    Product
    BMW — BMW 530I, 540I XDRIVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E097000·2024-11-18

    Limitless Van Recalls Rear Tire Mounts Due to Weld Failure Risk

    Limitless Van is recalling certain rear tire mounts because an improper weld may fail, allowing the mount to detach from the vehicle.

    Product
    EQUIPMENT:MECHANICAL:SPARE TIRE MOUNT/RACK recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V867000·2024-11-18

    KIA EV6 vehicles electric charging control unit damage risk

    Kia is recalling certain 2022–2024 EV6 vehicles because the Integrated Charging Control Unit may become damaged and stop charging the 12-volt battery, resulting in loss of drive power and increased crash risk.

    Product
    KIA — KIA EV6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E096000·2024-11-15

    BMW Recalls Oil Filters for Specific High-Performance Motorcycles

    BMW is recalling specific oil filters for S1000RR, M1000RR/R/XR, and HP4 (Race) motorcycles because vibration can cause them to unscrew, increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION:FILTER/SCREEN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide