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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

2851–2875 of 36527

SevereFDA (Food)·F-0572-2025·2025-03-05
Mombo's Vanilla Soft Serve Ice Cream Mix Recalled for Undeclared Egg Allergen
Arizona Foods Group is recalling Mombo's Vanilla Soft Serve Ice Cream Mix because it may contain egg, an undeclared allergen. Consumers with egg allergies should not consume this product.
Product
FOOD SERVICE - Mombo s Vanilla Soft Serve Ice Cream Mix, frozen & thawed for Ice cream machines. Packaged in a half gallon carton 64 oz and placed in cases of 6-units. Shelf-life is 18 months frozen / 30 days thawed refrigerated. Carton is a plain white carton with a sticker
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0579-2025·2025-03-05
Gerber Baby Soothe 'n' Chew Teething Sticks Recalled for Choking Risk
Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Banana flavor are recalled nationwide due to complaints of infant choking. All lots in both 1.59 oz and 3.2 oz packages are affected.
Product
Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
Category
Food
Distribution
46 states
SevereNHTSA·25V143000·2025-03-05
Airstream Recalls Classic Travel Trailers Due to Fire Risk
Airstream is recalling certain Classic travel trailers because the sofa footrest switch wiring may overheat, increasing the risk of a fire.
Product
AIRSTREAM — AIRSTREAM CLASSIC
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1196-2025·2025-03-05
Ventec VOCSN Ventilators Recalled Due to Incorrect Service Parts
Ventec Life Systems recalled VOCSN Multi-Function Ventilators (30 units in CA, NY, MO) due to incorrect parts used during service. Defects may cause unexpected shutdown or impaired respiratory monitoring and support.
Product
VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000, PRT-01185-002
Category
Medical Device
Distribution
3 states
SevereFDA (Food)·F-0577-2025·2025-03-05
Garden Salad Recalled for Undeclared Peanut Allergen in Florida and Georgia
FRESHPOINT CENTRAL FLORIDA, INC. is recalling Garden Salad 5 oz packages due to undeclared peanut allergen. The affected product was distributed in Florida and Georgia.
Product
Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300
Category
Food
Distribution
2 states
SevereNHTSA·25V138000·2025-03-03
Motiv Recalls School Buses Due to Throttle Position Sensor Defect
Motiv Power Systems is recalling certain 2017-2023 school buses because a loose throttle position sensor wire may cause a loss of drive power.
Product
MOTIV — MOTIV F-59 BEV CHASSIS SCHOOL BUS, E-450 BEV CHASSIS SCHOOL BUS, F-53 BEV CHASSIS SCHOOL BUS, F-59 SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V131000·2025-02-28
Ford Recalls 2022-2024 F-150 Lightning Vehicles Due to Battery Fire Risk
Ford is recalling 2022-2024 F-150 Lightning electric trucks because a manufacturing defect in the high-voltage battery cells may cause an internal short circuit, increasing the risk of a fire.
Product
FORD — FORD F-150 LIGHTNING BEV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V126000·2025-02-28
Ford EcoSport front half shafts can disconnect from the transmission
Ford is recalling certain 2021-2022 EcoSport vehicles because the front axle half shafts may disconnect from the transmission, causing a loss of drive power and a possible rollaway.
Product
FORD — FORD ECOSPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V127000·2025-02-28
Ford Maverick control modules may miss a low 12-volt battery
Ford is recalling certain 2022 Maverick vehicles previously repaired under 24V-590, because the body and powertrain control modules may fail to detect a change in 12-volt battery state of charge.
Product
FORD — FORD MAVERICK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V135000·2025-02-28
Mercedes Sprinter parking brake bracket welds can fail causing rollaway
Daimler Vans is recalling certain 2024 Mercedes-Benz Sprinter vehicles because the parking brake cable bracket welds may fail and disengage the parking brake, failing FMVSS 105.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V125000·2025-02-28
Audi Q4 e-tron on-board charger failure can cut drive power
Volkswagen is recalling certain 2024-2025 Audi Q4 e-Tron and 2024 ID.4 vehicles because the on-board charger may fail and stop charging the 12-volt battery, causing a loss of drive power.
Product
AUDI — AUDI, VOLKSWAGEN Q4 E-TRON, Q4 SPORTBACK E-TRON, ID.4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V130000·2025-02-28
Ford Recalls 2021-2022 Mustang Mach-E for Battery Contactor Overheating Risk
Ford is recalling 2021-2022 Mustang Mach-E vehicles previously repaired under recall 22V-412 because high voltage battery contactors may overheat, potentially causing loss of drive power and increasing crash risk.
Product
FORD — FORD MUSTANG MACH E
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V129000·2025-02-28
Mercedes-Benz Recalls Hybrid AMG Models Due to Software Error
Mercedes-Benz is recalling 2,943 hybrid AMG vehicles because a software error may cause the high-voltage starter alternator control unit to fail, resulting in a loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GT63 S E, AMG GLC63 S E 4MATIC+ COUPE, AMG S 63 E, AMG GT 63 S E COUPE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V133000·2025-02-28
Ford hybrids can shift into neutral unexpectedly losing drive power
Ford is recalling certain 2022-2024 Maverick, 2022 Escape and 2021-2022 Lincoln Corsair vehicles previously repaired under 24V-330, because hybrid powertrain software may shift the vehicle into neutral unexpectedly.
Product
FORD — FORD, LINCOLN MAVERICK, ESCAPE, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V132000·2025-02-28
Ford trucks may fail to apply electric trailer brakes
Ford is recalling certain 2021-2022 F-150, 2022 Maverick, Expedition, Navigator and Super Duty vehicles previously repaired under 22V-193, because a towed trailer's electric brakes may not apply.
Product
FORD — FORD, LINCOLN F-550 SD, F-350 SD, F-450 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·25157·2025-02-27
Gas boilers recalled for carbon monoxide poisoning risk; two deaths reported
Triangle Tube is recalling approximately 60,000 Prestige and Aerco Esteem gas boilers due to carbon monoxide release hazard. Two deaths and 25 CO leak incidents have been reported.
Product
Prestige Solo, Prestige Excellence, and Aerco Esteem condensing gas boilers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25159·2025-02-27
Goal Zero Solar Series Combiner Cables Recalled for Fire Hazard
Goal Zero LLC is recalling about 530 Solar Series Combiner Cables that can malfunction with Nomad-series solar panels and pose a fire hazard. The company has received two reports of fires involving property damage.
Product
Goal Zero Solar Series Combiner Cables for Solar Panels
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25165·2025-02-27
TRUBLUE auto belay systems recalled due to fall hazard risk
Head Rush Technologies is recalling approximately 410 TRUBLUE auto belay devices sold online from May 2023 through December 2024 because they can fail to retract, posing a fall hazard. One incident resulted in a fractured leg.
Product
TRUBLUE iQ and TRUBLUE iQ+ Auto Belays
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V121000·2025-02-27
Motorhome exhaust tips can detach letting fumes into the cabin
REV Recreation Group is recalling certain 2022-2025 Fleetwood and Holiday Rambler motorhomes because the engine exhaust tip may detach, allowing exhaust fumes to enter the cabin.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER SOUTHWIND, INVICTA, ADMIRAL, VACATIONER
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1070-2025·2025-02-26
Vascular Tack Endovascular System recalled for deployment and migration risks
Spectranetics' Intact Vascular Tack Endovascular System may fail to deploy properly or migrate in blood vessels, potentially causing ischemia and requiring additional intervention.
Product
Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm), 150cm, REF: 154150041; Tack, 4F Gen 1.5, 150cm CE, REF: 154150042; Tack, 4F Gen 1.5, 90cm CE, REF: 154090042 (6F, 3.5 - 6.0mm), 135cm, REF: 15613
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1152-2025·2025-02-26
Philips Allura Xper Patient Table Mattress Defect Fall Risk
Philips is recalling the Allura Xper FD10C patient examination table due to a mattress defect that may allow patients to fall from the table. The device was distributed worldwide.
Product
Allura Xper FD10C; Catalog number: 722001
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1144-2025·2025-02-26
Allura Xper FD20 Fluoroscopy Table Mattress Issue Causes Fall Risk
Philips recalls Allura Xper FD20 fluoroscopy patient tables due to a mattress issue that may cause patients to fall during procedures.
Product
Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1143-2025·2025-02-26
Philips Allura Xper Fluoroscopy Device Patient Table Mattress Fall Risk
Philips Medical is recalling certain Allura Xper FD10/10 fluoroscopy systems because the patient table mattress could cause patients to fall during procedures. The recall affects devices worldwide.
Product
Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1158-2025·2025-02-26
Philips Azurion 7 B20 imaging system patient fall hazard from table mattress
Philips Azurion 7 B20 imaging systems are recalled because the patient table mattress may allow patients to fall. This FDA Class I recall affects 1,314 units distributed worldwide.
Product
Azurion 7 B20; Catalog numbers: (1) 722068, (2) 722226, (3) 722236.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1148-2025·2025-02-26
Philips Allura Xper FD20/10 Imaging System Patient Table Mattress Fall Risk
Philips is recalling the Allura Xper FD20/10 imaging system due to a defect in the patient table mattress that could allow patients to fall during procedures. The Class I recall affects 87 units distributed globally, including 22 in the US.
Product
Allura Xper FD20/10; Catalog numbers: 722029
Category
Medical Device
Distribution
Distributed nationwide

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