All Product Recalls

Orthofix Recalls FORZA PTC Spacer System Over Labeling Issues

Labeling contains claims that are not consistently present.

GET TESTED INTERNATIONAL AB Recalls 16 Food Intolerance Test Medium Devices (2025)

Distribution without premarket approval/clearance.

Orthofix Recalls CONSTRUX Mini Ti Spacer System Over Labeling Issues

Orthofix U.S. recalled 40,956 units of the CONSTRUX Mini Ti Spacer System on November 3, 2025. Labeling inconsistencies pose potential risks to patients and healthcare providers. Users should stop using the device immediately and follow recall instructions.

Orthofix Recalls CONSTRUX Mini PTC Spacer System Due to Labeling Issues

Labeling contains claims that are not consistently present.

Orthofix Recalls Ti Spacer System Due to Labeling Issues

Labeling contains claims that are not consistently present.

Medtronic MiniMed 780G Insulin Pump Recalled Over Software Issue

A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery.

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

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 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.

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

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.

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

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

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue MX600 Patient Monitor Recall 2025 for Alarm Failure

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.

Nivagen Zinc Oxide Ointment Recalled Due to cGMP Deviations

Philips Ultrasound System Recalled Over Compatibility Issues

Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.

Philips IntelliVue Patient Monitor MX800 Recalled for Alarm Failure

Potential issue where the IntelliVue monitors did not alarm.

Stryker Recalls 39,148 NICO BrainPath BrainPath Shephard's Hook Devices Over Latex Packaging (2026)

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