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
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
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 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
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
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
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
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
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
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
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
HIGH
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
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella Controller AIC Recall 2025 Affects 71 Units Across 6 Regions
Specific Automated Impella Controllers (AICs) that have a Pump Driver Circuit Assembly do not meet current specifications. This may lead to decreased pump performance or pump stop and trigger an Impella Failure or Impella Stopped Controller Failure alarm.
Abiomed
Specific Automated
Food & Beverages
HIGH
FDA FOOD
60,630 Hostess Ding Dongs Recalled for Mold Risk — Check Your Best If Use By Dates
Mold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.
The J.M. Smucker
Mold. The
Health & Personal Care
HIGH
FDA DRUG
Carvedilol Tablets 12.5 mg Recall Expanded for NNCI Impurity Above FDA Limit (2025)
The FDA recalls 26,628 cartons of Carvedilol Tablets USP 12.5 mg distributed nationwide. The product fails CGMP standards due to NNCI impurity exceeding FDA limits. Stop using and contact The Harvard Drug Group LLC and Rugby Laboratories for guidance.
Major Pharmaceuticals
CGMP Deviations:
Food & Beverages
HIGH
FDA FOOD
Jessie Lord Bakery Lemon Meringue Pie Recall 136,252 Cases Over Undeclared Yellow #5 (2025)
Jessie Lord Bakery is recalling 136,252 cases of Lemon Meringue Pie sold at retailers in 14 states due to undeclared Yellow #5. The dye was not disclosed on packaging. Consumers should not eat the product and should seek a refund or replacement.
Jessie Lord Bakery
Undeclared Yellow#5
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
Food & Beverages
HIGH
FDA FOOD
Itacate Foods CAMPSITE LENTEJAS Lentil Soup Recalled for Undeclared Yellow Dyes (154 Packages, 2025)
Itacate Foods
Undeclared Yellow
Tag Statistics
Total Recalls
2,229