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

17576–17600 of 27769

HighFDA (Devices)·Z-2101-2023·2023-07-12
Giraffe OmniBed neonatal incubator recall due to incorrect secondary latch installation
GE HealthCare is recalling Giraffe OmniBed neonatal incubators with potentially incorrect secondary latches on bedside panels. An incorrect latch type may have been installed on northeast and/or northwest panels of affected units.
Product
Giraffe OmniBed, with the following Model Numbers: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, 6650-0094-901, 6650-0001-9901, 6650-0029-901, 6650-0080-901, 6650-0032-901, 6650-0077-901, 6650-001-901, 6650-0006-901, 6650-0129-901, 6650-0063-902, 6650-0130-901, 6650
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2079-2023·2023-07-12
Dermal Repair Scaffold Recalled Due to Endotoxin Testing Issues
TEI Biosciences is recalling PriMatrix Meshed dermal repair scaffolds due to endotoxin testing failures. The recall affects 33,277 units distributed nationwide.
Product
PriMatrix Meshed; Dermal Repair Scaffold; Rx Only; Sizes 20x25 cm (1:1), 3x3 cm (2:1), 4x4 cm (2:1), 5x5 cm (2:1), 6x6 cm (2:1), 8x12 cm (2:1), and 8x8 cm (2:1).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2058-2023·2023-07-12
Treadmill recalled for drive PCB malfunction causing unexpected acceleration
Full Vision Inc recalls 95 TRACKMASTER GE T2100-ST2 treadmills with a defective drive PCB that may misread signals, causing the equipment to unexpectedly stop, reverse, or accelerate forward.
Product
TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2072-2023·2023-07-12
SurgiMend 2.0 Collagen Matrix Recalled for Endotoxin Testing Issues
TEI Biosciences is recalling SurgiMend 2.0 collagen matrices nationwide due to possible out-of-specification endotoxin test results from issues with in-process and finished goods testing procedures.
Product
SurgiMend 2.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x20 cm, 20x25cm, 10x15cm Semi-Oval,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1229-2023·2023-07-12
Pearl Milling Company Corn Meal Mix Recalled for Undeclared Milk
Pearl Milling Company Self-Rising Yellow Corn Meal Mix bags may contain undeclared milk, posing a risk to people with milk allergies. Approximately 91,760 bags were distributed across multiple US states.
Product
Pearl Milling Company Self-Rising Yellow Corn Meal Mix Net Wt 80 oz (5 lb) UPC 3000057380 packaged in paper bag with printed label
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2086-2023·2023-07-12
Medical procedure packs recalled for compromised package seals
DeRoyal Industries is recalling 4,225 custom medical procedure packs nationwide because outer package seals may be open or compromised, potentially affecting sterility of the surgical materials inside.
Product
Custom medical procedure packs labeled as: a) OPEN HEART TRACECART, REF '53-1941; b) CARDIAC CATH PACK, REF '89-10045; c) SHOULDER PACK, REF '89-10115; d) MINOR ORTHO PACK, REF '89-10213; e) TOTAL KNEE PACK PGYBK, REF '89-10505; f) ANTERIOR HIP PACK PGYBK, REF '89
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1074-2023·2023-07-12
Breader Product Recalled Due to Potential Salmonella Contamination
Newly Weds Foods is recalling B50413 Breader X3 products due to potential Salmonella contamination. No illnesses have been reported.
Product
B50413 BREADER X3 50.00 BAG
Category
Food
Distribution
0 states
HighFDA (Food)·F-1024-2023·2023-07-12
Cricket Creek Farm Berkshire Bloom Cheese Recalled for Improper Pasteurization
Cricket Creek Farm Berkshire Bloom Cheese has been recalled because it was not properly pasteurized. Batch #076 (140 units) was distributed in New York, Massachusetts, and Connecticut.
Product
Cricket Creek Farm brand Berkshire Bloom Cheese
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2105-2023·2023-07-12
Stryker Infinity Alignment Frame Distal Sub-Assembly Recalled for Manufacturing Defect
Wright Medical Technology is recalling the Stryker Infinity Alignment Frame Distal Sub-Assembly due to manufacturing defects that prevent proper assembly. The pin sleeve holes were manufactured too narrow, preventing insertion of pin sleeves and proper device configuration.
Product
Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2080-2023·2023-07-12
PriMatrix Ag Dermal Repair Scaffold Recalled for Endotoxin Testing Issues
TEI Biosciences is recalling 1,689 units of PriMatrix Ag dermal repair scaffolds distributed nationwide due to potential endotoxin testing deficiencies. Testing procedures may not have been conducted reliably.
Product
PriMatrix Ag; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2099-2023·2023-07-12
BD Synapsys Informatics Solution risks patient data mis-association
The BD Synapsys Informatics Solution may incorrectly associate patient demographic data under specific conditions when the system operates near capacity during rapid manual result processing.
Product
BD Synapsys Informatics Solution, Catalog Number 444150
Category
Medical Device
Distribution
15 states
HighFDA (Food)·F-1035-2023·2023-07-12
Newly Weds Foods Batter Mix Recalled for Possible Salmonella Contamination
Newly Weds Foods, Inc. has recalled batter mix products that may contain Salmonella. Consumers should not use affected products and should consult the FDA for details.
Product
A29365 BATTER MIX X2 50.00 BAG
Category
Food
Distribution
0 states
HighFDA (Food)·F-1223-2023·2023-07-12
Cargill Tripotassium Citrate Monohydrate Recalled for Potential Metal Contamination
Cargill is recalling Tripotassium Citrate Monohydrate in 50 lb. bags due to potential metal contamination. The product was distributed to manufacturers and distributors across multiple states and Canada.
Product
Cargill Tripotassium Citrate Monohydrate packaged in 50 lb. paper bag. Product item: SKU 100105392, TPC GNLR 50LB BG KH FCC
Category
Food
Distribution
13 states
HighFDA (Drugs)·D-0895-2023·2023-07-12
Losartan Potassium Tablets Recalled for Blue Plastic Contamination
Strides Pharma Inc. is recalling Losartan Potassium Tablets, 25 mg, due to the presence of blue plastic pieces embedded in tablets from lot 7901903A. No illnesses or injuries have been reported.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V785000·2023-07-10
Spartan K2 RV Chassis Recalled for Undersized Air Brake Reservoir
Shyft Group is recalling certain 2021-2023 Spartan K2 RV Chassis due to undersized air brake supply reservoirs that may fail to provide sufficient air for proper brake operation, increasing crash risk.
Product
SPARTAN — 2022 SPARTAN K2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V784000·2023-07-10
2023 Thor Motor Coach Magnitude and Omni Motorhomes Recalled for Seat Belt Label Error
Thor Motor Coach is recalling certain 2023 Magnitude and Omni motorhomes because the occupant capacity label incorrectly lists seat belt quantity. Occupants could be transported without sufficient available seat belts.
Product
THOR MOTOR COACH — 2023 THOR MOTOR COACH MAGNITUDE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V623000·2023-07-09
2023-2024 Alfa Romeo Tonale plug-in hybrid electric vehicles recalled for fire risk
Chrysler is recalling 2023-2024 Alfa Romeo Tonale and Dodge Hornet plug-in hybrid electric vehicles. Improperly tightened battery and high voltage connector cables can overheat and cause fires while parked or driving.
Product
ALFA ROMEO — 2023 ALFA ROMEO TONALE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V703000·2023-07-09
2016-2023 Kia Sorento and Sportage tow hitch electrical fire hazard recall
Kia is recalling certain 2016-2023 Sorento and 2017-2022 Sportage models with factory or dealer-installed tow hitch harnesses. Moisture and debris on the harness module can cause an electrical short and fire while parked or driving.
Product
KIA — 2016 KIA SORENTO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V702000·2023-07-09
Tesla Model 3 window automatic reversal system may pinch occupants
Tesla recalls 2017–2022 Model 3, 2020–2022 Model Y, and 2021–2022 Model S/X vehicles whose automatic window reversal system may fail to detect obstructions and pinch occupants. A free software update will fix the issue.
Product
TESLA — 2020 TESLA MODEL 3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V622000·2023-07-09
2023-2024 BMW Models Recall: Front Passenger Knee Air Bag Deployment Failure
BMW is recalling certain 2023 BMW XM and 2024 BMW X5, X6, X7, and Alpina XB7 vehicles because the front passenger knee air bag may not deploy as intended, increasing injury risk in a crash.
Product
BMW — 2023 BMW XM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V559000·2023-07-08
2024 Forest River Sierra and Sandpiper Braking System Defect
Forest River is recalling certain 2024 Sierra and Sandpiper fifth wheels due to backwards axle installation that reduces braking ability and increases crash risk. Dealers will reinstall the axle at no cost.
Product
FOREST RIVER — 2024 FOREST RIVER SIERRA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V677000·2023-07-08
Power Steering Pump Defect in 2021 Autocar Xpeditor Vehicles
Autocar is recalling 2021 Xpeditor and certain 2020-2021 Legend vehicles due to a power steering pump defect that can cause loss of power steering assist and increase crash risk.
Product
AUTOCAR — 2021 AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V509000·2023-07-07
2022 Kia Sorento and Telluride recalled for spare tire brake defect
Kia is recalling 2022 Sorento and Telluride vehicles with an incorrect spare tire that can impair the anti-lock braking and traction control systems. These defects increase the risk of a crash.
Product
KIA — 2022 KIA SORENTO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V469000·2023-07-07
Newmar motorhomes recalled for defective seat belt mounting brackets
Newmar is recalling certain 2019–2023 motorhomes because modified seat belt mounting brackets can fail to properly restrain occupants in a crash, violating federal safety standards.
Product
NEWMAR — 2023 NEWMAR BAY STAR SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V468000·2023-07-07
2023 Toyota Tundra Spare Tire Carrier May Detach Due to Insufficient Welds
Toyota is recalling certain 2023 Tundra, Tundra Hybrid, and Sequoia Hybrid vehicles due to insufficiently welded spare tire carrier assemblies that may break and allow the spare tire to detach, increasing crash risk.
Product
TOYOTA — 2023 TOYOTA TUNDRA
Category
Vehicle
Distribution
Distributed nationwide

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17576–17600 of 27769