Omnipod 5 App recalled due to a software error which occurs when users input bolus amounts below 1 unit without adding a zero before the decimal point.

2024 Medical Device Recalls

On December 13, 2023, Getinge / Atrium Medical Corporation notified affected customers of a nationwide recall (medical device correction) for certain Atrium Express Dry Suction Dry Seal Chest Drains in response to a voluntary medical device recall initiated by a supplier, Nurse Assist. On November

Listing of Medical Device 2024 Safety Communications

This device has significantly changed since FDA authorization, and the safety and effectiveness of the modified device has not been established.

Herpes simplex virus-2 serological tests can produce false reactive results especially if a person has a low risk of infection or if test results are near the test’s cut-off.

The FDA posts letters to health care providers about the safe use of medical devices.