electronic Recalls

Philips IntelliVue M3002A Recall Over Alarm Failure Affects 1,913,441 Units (2025)

Potential issue where the IntelliVue monitors did not alarm.

PHILIPS IntelliVue MP80 Recall 1,913,441 Monitors Worldwide for Alarm Failure (2025)

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue MX700 Recall Affects 1,913,441 Monitors Worldwide (2025)

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue MP50 Recall 2025 Over Alarm Failure in 1.9 Million Monitors

Potential issue where the IntelliVue monitors did not alarm.

Knog Blinder 900 and Blinder 1300 Bike Lights Recalled for Fire Hazard (2025)

Olympus HX-400U-30 Recall: 7,803 Endoscopic Ligation Devices Recalled in 2025

Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy.

B. Braun Medical Blood Administration Set Recall 7,344 Units Over Backflow Risk (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B Braun Medical Blood Administration Set Recall 2025 for 24,624 Units Worldwide

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical IV Administration Set Recall Affects 286,400 Units Across Global Pumps (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical Recalls 7,008 IV Administration Sets for Infusomat Space Pumps (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical IV Administration Set Recall 122,232 Units Over Backflow Risk (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical IV Administration Set Recalled for 126,050 Units Over Backflow Risk (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

BBMI IV Administration Sets Recalled in 2025 for Backflow and Occlusion Risk, 20.7 Million Units

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical Recalls 9,500 IV Administration Sets for Backflow and Occlusion Risk (2025 Recall)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B Braun Medical IV Administration Set Recall 11,832 Units Over Backflow Risk (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical IV Administration Set Recalled for Backflow Risk in 65,904 Units (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B Braun Medical IV Administration Set Recall for 4,488 Units in 2025

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

Illumina NextSeq 550Dx Reagent Kits Recalled for Leaky Flow Cells Affecting 11,916 Units Worldwide

Bio Ionic 1-Inch Curling Iron Recalled for Burn Hazard (2025)

Bio Ionic recalls the 1-Inch-Long Barrel Curling Iron model LXT-CL-1.0 with date code 0722-1223. The recall is active as of 2025-10-23. Consumers should stop using the recalled curling iron and contact Bio Ionic for a free replacement.

Lifepro Bioremedy Infrared Sauna Blankets Recalled for Burn Hazard (2025)