suffocation risk Recalls

Siemens MRI Recall: 18 MAGNETOM Skyra Fit BioMatrix Systems Recalled Over Helium Vent Blockage Risk

Siemens MAGNETOM Skyra fit MRI Recalled for Ice Blockage Risk in 30 Units (2025)

Chlorpromazine Hydrochloride 25 mg Tablets Recalled Nationwide Over Foreign Substance in Packaging

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

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.

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

Cross Contamination with Other Products.

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.

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.

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.

Frontier Devices 301.916S1 16 mm Distraction Pin Recall Expanded (2025)

Labeling includes shelf life that has not been validated.

Frontier Devices Recalls 2,700 REF 301.914S1 14 mm Distraction Pins (2025)

Labeling includes shelf life that has not been validated.

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.

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.

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 Recalls 160 301.912S2 12 mm Distraction Pin Over Unvalidated Shelf-Life Labeling (Z

Labeling includes shelf life that has not been validated.

Bard Peripheral Vascular Venclose DigiRF Generator Recall Affects 1,725 Units Worldwide

Mercedes-Benz GLC 350E 4MATIC Recall for Steering Fasteners Affects 2023-2026 Models

Mercedes-Benz USA recalls 2025 GLC 350E 4MATIC and related EQE/GLC models due to a loose steering coupling bolt. The defect may loosen the steering rack, risking loss of control. Dealers will tighten bolts at no charge. MBUSA notified owners on Oct 6, 2025.

Itacate Foods LLC Recalls CHARGE-UP CHILAQUILES for Undeclared Yellow #5 and Yellow #6

Itacate Foods LLC recalls 566 packages of CHARGE-UP CHILAQUILES distributed to multiple U.S. states for undeclared Yellow #5 and Yellow #6 color additives. The recall is active as of September 24, 2025. No injuries are reported in the recall notice.

Boston Scientific Pacemakers Recall 28,911 U128 ACCOLADE, VISIONIST VALITUDE CRT-P Devices (2025)

Boston Scientific Pacemakers Recall 1,380 Units Over Software Safety Issue