cpsc regulated Recalls

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 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.

Hyundai Recalls 2025-2026 Santa Fe and Tucson for Engine Fastener Issue

Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Tucson and Santa Fe vehicles. The connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power and engine damage, possibly resulting in an oil leak.

GORE ACUSEAL Vascular Graft Recall Affects 52,306 Devices Worldwide (2025)

Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV

Shell egg product potentially contaminated with salmonella.

Chlorpromazine Hydrochloride 100 mg Recall Affects 2,003 Cartons Nationwide for Foreign Substance

Presence of a foreign substance.

TopCare Health 70% Isopropyl Alcohol Recall Expands to 60 Bottles Nationwide (2025)

Cross Contamination with Other Products.

AvKare Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Foreign Substance Contamination (2025

Presence of a foreign substance.

Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk

Cross Contamination with Other Products.

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.

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.

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

One lot manufactured with an invalid sterilization cycle.

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.

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 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.

CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)

One lot manufactured with an invalid sterilization cycle.

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.

GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)

Frontier Devices 301.914S1 Distraction Pin Recall: 10,960 Units Due to Labeling Issue

Labeling includes shelf life that has not been validated.

Taylor Farms Retail Salad Kit Recalled for Undeclared Sesame and Soy Allergens (2025)

Undeclared allergens (sesame and soy).