Food & Beverages
HIGH
FDA FOOD
Extract Labs Elderberry 20mg CBD Gummies Recalled for Peanut Cross-Contact Risk (19,720 Units) 2025
Extract Labs
Potential peanut
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Health & Personal Care
HIGH
FDA DRUG
B. Braun Medical 3000 mL Saline Irrigation Bags Recalled for Sterility Concerns
Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.
B. Braun Medical Inc.
Lack of
Food & Beverages
HIGH
FDA FOOD
Extract Labs Blue Razz 20mg CBD/THC Gummies Recall 2025 for Peanut Cross-Contact — 19,810 Units
Extract Labs
Potential peanut
Health & Personal Care
HIGH
FDA DRUG
B. Braun Sterile Water for Injection 3000 mL Recall Affects 26,316 Bags Over Sterility Concerns (202
Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.
B Brau Medical Inc.
Lack of
Food & Beverages
HIGH
FDA FOOD
Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV
Shell egg product potentially contaminated with salmonella.
Country Eggs
Shell egg
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DRUG
TopCare Health 70% Isopropyl Alcohol Recall Expands to 60 Bottles Nationwide (2025)
Cross Contamination with Other Products.
TopCare Health
Cross Contamination
Health & Personal Care
HIGH
FDA DRUG
Chlorpromazine Hydrochloride 100 mg Recall Affects 2,003 Cartons Nationwide for Foreign Substance
Presence of a foreign substance.
CHLORPROMAZINE HYDROCHLORIDE
Presence of
Vehicles & Parts
HIGH
NHTSA
Kia 2025 K4 and Sorento Recalled for Engine Fasteners SC349
Kia America, Inc. (Kia) is recalling certain 2025 K4 and Sorento vehicles. The connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power.
Kia
A loss
Health & Personal Care
HIGH
FDA DRUG
AvKare Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Foreign Substance Contamination (2025
Presence of a foreign substance.
AvKare
Presence of
Health & Personal Care
HIGH
FDA DRUG
Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk
Cross Contamination with Other Products.
Kroger
Cross Contamination
Health & Personal Care
HIGH
FDA DEVICE
LeMaitre Vascular Artegraft 10-Unit Recall 2025 for Labeling Errors
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
LeMaitre Vascular
Devices were
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DEVICE
CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle
One lot manufactured with an invalid sterilization cycle.
CooperVision
One lot
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DEVICE
CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)
One lot manufactured with an invalid sterilization cycle.
CooperVision
One lot
Vehicles & Parts
HIGH
NHTSA
Ford 2025-2026 F-Series Recalled for Instrument Panel IPC Start-Up Failure (25S88)
Ford Motor Company (Ford) is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles. The Instrument Panel Cluster (IPC) may fail at startup.
Ford
An instrument
Health & Personal Care
HIGH
FDA DRUG
Ultra Violette Mini Mates SPF 50 Kit Recalled for SPF Variability in 44,497 Tubes (2025)
Ultra Violette Mini Mates SPF 50 kit sold nationwide in the U.S. is recalled. Testing showed SPF results ranging from 4 to 64. The recall is issued by Grace & Fire USA Inc. The public was notified by letter.
ULTRA VIOLETTE MINI MATES
Subpotent/Super-potent Product:
Health & Personal Care
HIGH
FDA DRUG
Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected
Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.
ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN
Subpotent/Super-potent Product:
Health & Personal Care
HIGH
FDA DEVICE
CooperVision MyDay Toric Contact Lenses Recalled for Invalid Sterilization Cycle
CooperVision recalled 4,140 MyDay Toric contact lenses sold nationwide in the United States. The recall cites an invalid sterilization cycle for one lot. Patients should stop wearing the lenses and consult their eye care providers for guidance.
CooperVision
One lot