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

13226–13250 of 31489

ModerateFDA (Devices)·Z-2019-2024·2024-06-12
Quality Control Tool Vitamin B12 Range Verifier Recalled by FDA
Ortho-Clinical Diagnostics is recalling VITROS Vitamin B12 Range Verifier Lot 1200 because the product may fail to verify required calibration range. The failure is detectable during use and does not affect actual patient test results.
Product
VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used for the quantitative measurement of v
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0540-2024·2024-06-12
Cephalexin oral suspension recalled for incorrect dose labeling
Bryant Ranch Prepack is recalling 61 bottles of Cephalexin for Oral Suspension due to a back label stating an incorrect dose amount—5g instead of 10g per bottle.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2026-2024·2024-06-12
Surgical imaging device electrical component may intermittently shut off
The O-arm O2 surgical imaging system may experience intermittent electrical failure affecting intraoperative imaging guidance. The recall involves 20 units distributed in the US and internationally.
Product
O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and pediatric patients. Product Number: BI70002000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1284-2024·2024-06-12
Charles Boggini Pink Lemonade Recalled for Undeclared Food Dye
Charles Boggini Pink Lemonade in 1 and 5-gallon sizes is recalled for containing undeclared FD&C Red No. 40. The colorant was not listed on product labels.
Product
Charles Boggini Pink Lemonde; 1 or 5 U.S. Gallons
Category
Food
Distribution
9 states
ModerateFDA (Drugs)·D-0537-2024·2024-06-12
Cephalexin oral suspension recalled for incorrect label dosage amount
Bryant Ranch Prepack is recalling Cephalexin oral suspension (125mg/5mL) due to back label errors stating the dose as 2.5g instead of the correct 5g per bottle. No illnesses have been reported.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0543-2024·2024-06-12
Estradiol transdermal patches recalled for failed quality specifications
Zydus Pharmaceuticals is recalling 13,440 units of Estradiol transdermal patches distributed nationwide due to failed impurities and degradation specifications. No illnesses or injuries have been reported.
Product
ESTRADIOL — ESTRADIOL (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0542-2024·2024-06-12
Estradiol Transdermal Patch Recalled for Failed Chemical Specifications
Zydus Pharmaceuticals is recalling Estradiol Transdermal System patches nationwide due to failed impurities and degradation specifications. The recall affects 21,360 units distributed throughout the United States.
Product
ESTRADIOL — ESTRADIOL (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1947-2024·2024-06-12
Leica HistoCore PEGASUS tissue processor recalled for tissue damage
LEICA BIOSYSTEMS is recalling 141 Leica HistoCore PEGASUS tissue processors due to reagent overfilling that causes poorly processed or damaged biopsy tissue specimens.
Product
Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0544-2024·2024-06-12
TIVICAY HIV medication carton mislabeled with incorrect expiration date
GlaxoSmithKline recalls TIVICAY cartons nationwide with incorrect expiration date on packaging. The carton label shows May 2026, but the correct expiration on the bottle is April 2025.
Product
TIVICAY — TIVICAY (DOLUTEGRAVIR SODIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0536-2024·2024-06-12
Cephalexin Oral Suspension Recalled for Incorrect Labeling and Missing Dosage Information
Bryant Ranch Prepack is recalling Cephalexin oral suspension bottles due to incorrect labeling that states tablet information instead of liquid suspension details and omits the total dose per bottle.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0539-2024·2024-06-12
Cephalexin for Oral Suspension Recalled for Back Label Error
Cephalexin for Oral Suspension is being recalled due to a back label error. The label states 'Each contains' instead of 'Each Bottle contains,' affecting 190 bottles distributed nationwide.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V837000·2024-06-11
PJ TRAILERS LD trailers recalled for incorrectly installed brake axles
PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.
Product
PJ TRAILERS — 2025 PJ TRAILERS LD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V826000·2024-06-11
Winnebago and Itasca Recreational Vehicles Recalled for Hood Bracket Detachment
Winnebago Industries is recalling certain 2014-2025 RVs because hood bracket adhesive may have been incorrectly applied, allowing the bracket to detach and create a crash hazard. Dealers will provide free inspection and repair.
Product
WINNEBAGO — 2025 WINNEBAGO SUNSTAR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V700000·2024-06-10
BMW 750e and multiple 2023-2024 models recalled for steering wheel sensor defect
BMW is recalling certain 2023-2024 models including the 750e due to a faulty ground connection in the steering wheel electrical system. The defect may render the hands-on detection system inoperative, preventing the emergency stopping assistant from engaging and increasing crash risk.
Product
BMW — 2024 BMW 750E
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V728000·2024-06-09
Crossroads and Dutchmen Trailers Recalled for Loose Axle U-Bolts
Keystone RV is recalling 2021-2022 Crossroads Redwood, Dutchmen Voltage, and Yukon trailers for improperly tightened axle U-bolts that may cause loss of vehicle control and crash risk.
Product
CROSSROADS — 2021 CROSSROADS REDWOOD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V640000·2024-06-09
2023 Dodge Durango Shifter Interference Can Cause Sudden Power Loss
Chrysler is recalling certain 2023 Dodge Durango Pursuit vehicles because the shifter may slip out of gear while driving, causing sudden loss of drive power and increasing crash risk.
Product
DODGE — 2023 DODGE DURANGO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V641000·2024-06-09
Jeep Wrangler and Gladiator reverse lights and camera failure recall
Certain 2022-2023 Jeep Wrangler and Gladiator vehicles with manual transmission have a defective gear position sensor that may prevent the rearview camera from displaying and the reverse lights from illuminating, creating a visibility and safety hazard.
Product
JEEP — 2022 JEEP WRANGLER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V729000·2024-06-09
2021-2022 Forest River Travel Trailers: Fresh Water Tank Dislodgement
Forest River is recalling 2021-2022 Ozark, Wildwood, and Salem travel trailers because the fresh water tank may dislodge when full or overfilled, creating a road hazard and increasing crash risk.
Product
FOREST RIVER — 2021 FOREST RIVER OZARK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V655000·2024-06-09
Phoenix Motorcars Transit Buses Recalled for Electrical System Fire Risk
Phoenix Motorcars is recalling certain 2019-2021 800V Catalyst and 2020-2022 ZX5 transit buses. The vehicle software may cause the radiator fan electrical circuit to overheat, increasing fire risk.
Product
PROTERRA — 2020 PROTERRA ZX5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V731000·2024-06-09
Ford F-53 Rear Stabilizer Brackets May Separate from Vehicle
Ford is recalling 2020-2021 F-53 recreational vehicles because rear stabilizer bar attachment brackets may break and separate, creating a road hazard and increasing crash risk. Dealers will inspect and replace the brackets free of charge.
Product
FORD — 2020 FORD F53
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V733000·2024-06-09
2020 Mercedes-Benz CLS450 improperly secured battery defect recall
Mercedes-Benz is recalling 2019-2022 CLS450 and related models. The 12V battery in the trunk may not be properly secured, which could cause electrical failure and disable safety features like the emergency call system, hazard lights, and automatic door locks in a crash.
Product
MERCEDES-BENZ — 2020 MERCEDES-BENZ CLS450
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V730000·2024-06-09
2022 Ford Maverick brake lights may illuminate unintended due to ABS defect
Ford is recalling 2022 Maverick vehicles with an ABS module defect that may cause brake lights to illuminate without driver input. This could confuse other drivers and increase crash risk.
Product
FORD — 2022 FORD MAVERICK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V589000·2024-06-08
2021-2023 Hyundai Elantra HEV unintended acceleration software defect
Hyundai is recalling certain 2021-2023 Elantra HEV vehicles due to a software error in the motor control unit that may cause unintended acceleration after releasing the brake pedal, increasing crash risk.
Product
HYUNDAI — 2021 HYUNDAI ELANTRA HEV
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V655000·2024-06-08
Motorhomes with improperly routed hydraulic lines pose fire risk
REV is recalling 2018-2023 motorhome models from Fleetwood and Holiday Rambler because hydraulic lines may be improperly routed or protected, risking fluid leaks that could cause fires. Dealers will repair free of charge.
Product
FLEETWOOD — 2020 FLEETWOOD BOUNDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V496000·2024-06-07
2021 Nissan Kicks vehicles recalled for power steering defect
Nissan is recalling 2021 Kicks vehicles due to an intermittent electrical connection in the power steering system that can disable power steering assist. Loss of power steering increases steering effort and crash risk.
Product
NISSAN — 2021 NISSAN KICKS
Category
Vehicle
Distribution
Distributed nationwide

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13226–13250 of 31489