Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)
GE Medical Systems
If a
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,434
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Health & Personal Care
HIGH
FDA DEVICE
Abbott i-STAT CG8+ Cartridge Recall 2025: 8,962,450 Units
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Abbott Point Of Care i-STAT EG7+ Cartridges Recalled Over 6.1 Million Units in 2025
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Abbott i-STAT CG8+, EG7+, EG6+ Cartridges Recalled in 2025 Over Missing 510(k) Clearance
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.916S1 16 mm Distraction Pin Recall Expanded (2025)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.914S2 14 mm Distraction Pin Recalled for Unvalidated Shelf Life (High Risk)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Vehicles & Parts
HIGH
NHTSA
Chevrolet Corvette 2025 Recall for Fuel System Fire Risk After Refueling Spill
General Motors, LLC (GM) is recalling certain 2023–2026 Chevrolet Corvette vehicles equipped with a left-side radiator/fan combination. Excess fuel may spill into the vehicle fuel-filler pocket during refueling and leak onto an ignition source.
Chevrolet
A fuel
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices Recalls 160 301.912S2 12 mm Distraction Pin Over Unvalidated Shelf-Life Labeling (Z
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices Recalls 2,700 REF 301.914S1 14 mm Distraction Pins (2025)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Food & Beverages
HIGH
FDA FOOD
Latitude 36 Foods Honey Balsamic Dressing Recalled for 46,800 Units in 2025
Product contains undeclared Soy and Sesame
Latitude 36 Foods
Product contains
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Abbott i-STAT CG4+ Cartridge Recall: 9,067,050 Units Across U.S. With 510(k) Clearance Issue (2025)
Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.912S1 12 mm Distraction Pin Recall Expanded to 3,790 Units (Rx Only)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Food & Beverages
HIGH
FDA FOOD
Taylor Farms Retail Salad Kit Recalled for Undeclared Sesame and Soy Allergens (2025)
Undeclared allergens (sesame and soy).
Taylor Farms Retail
Undeclared allergens
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.914S1 Distraction Pin Recall: 10,960 Units Due to Labeling Issue
Labeling includes shelf life that has not been validated.
Folsom Metal Products
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls 828 Valve Pack-LF Cannula Kits DYNJ0415366P and DYNJ0415366Q (2025)
The kits contain certain lots of cannula products where the catheter may not retain its shape.
Medline Industries
The kits
Health & Personal Care
HIGH
FDA DEVICE
Bard Peripheral Vascular Venclose DigiRF Generator Recall Affects 1,725 Units Worldwide
Bard Peripheral Vascular
Software version
Food & Beverages
HIGH
FDA FOOD
Itacate Foods CAMPSITE LENTEJAS Lentil Soup Recalled for Undeclared Yellow Dyes (154 Packages, 2025)
Itacate Foods
Undeclared Yellow
Health & Personal Care
HIGH
FDA DRUG
96 Bottles of Sulfamethoxazole and Trimethoprim Tablets Recalled for Micro-Organism Contamination
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
Health & Personal Care
HIGH
FDA DRUG
Baxter Acetaminophen Injection 1000 mg/100 mL Recall for Discoloration
Baxter Healthcare’s Acetaminophen Injection 1000 mg/100 mL is recalled. The nationwide recall covers 13,000 containers with lot 24A27G66 and expiring 12/31/2025. The FDA lists discoloration as the hazard. Stop using and contact Baxter or a healthcare provider.
Baxter Healthcare Corporation
Discoloration