replacement available Recalls

Philips IntelliVue MX600 Patient Monitor Recall 2025 for Alarm Failure

Potential issue where the IntelliVue monitors did not alarm.

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 MP50 Recall 2025 Over Alarm Failure in 1.9 Million Monitors

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue MP2 Monitors Recalled for Alarm Failure in 2025 (1,913,441 Units)

Philips North America is recalling 1,913,441 IntelliVue MP2 patient monitors worldwide. The devices may fail to alarm when critical conditions arise. Hospitals should stop using the monitors and follow Philips recall instructions.

Aizu Olympus OER-Elite Medical Device Recall Affects 6,578 US Units (2025)

Philips IntelliVue MP20 Recall Expands to 1.9 Million Units Over Alarm Failure Risk (2025)

Philips recalls 1.913 million IntelliVue MP20 patient monitors worldwide because the devices may fail to alarm. The issue could prevent critical alerts from sounding. Hospitals should stop using the monitors immediately and follow Philips recall instructions.

Philips IntelliVue MP60 Recall for Alarm Failure Affects 1,913,441 Monitors (2025)

Philips North America is recalling 1,913,441 IntelliVue MP60 patient monitors. The monitors may fail to alarm as designed. Hospitals and clinics using MP60 units should stop using the devices and follow the recall instructions.

Philips IntelliVue MP40 Recall 1.9M Monitors Over Alarm Failure (2025)

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue MP5 M8105A Recall: 1,913,441 Monitors Worldwide Alarm Failure (2025)

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue MX100 Patient Monitors Recalled for Alarm Failure (Z-0861-2026)

Potential issue where the IntelliVue monitors did not alarm.

Blonde Beard's Dojo Asian Wing Sauce Recalled for Undeclared Soy (2025)

STRYKER NICO Myriad Handpiece Recall for 39,148 Units Worldwide (2026)

Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.

Werner Paddles Recalls Stealth & Covert Kayak Paddles Over Drowning Hazard (2025)

This recall involves models Stealth and Covert kayak paddles. The brand name Werner appears on decals on both blades and the model name is printed on the right paddle blade. The paddles are made of black carbon fiber.

Crate & Barrel Recalls Ana Dining Chairs Across 15 SKUs for Fall Hazard (2025)

Grundens Recalls Youth Clipper 282 and Zenith 282 Jackets Over Drawstrings Strangulation Hazard (202

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.

Harppa 5-in-1 Convertible High Chair Recall Expands Over Risk of Fall and Entrapment Hazards (2025)

B Braun Medical Recalls 19,104 IV Administration Sets for Backflow Risk (2025)

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