Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 241–260 of 1,000 recalls
Siemens Medical Solutions USA, Inc
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the Patient Marking step.
WHPM Inc.
Frm became aware that a customer complaint was reported to US FDA that SARS-CoV-2 Antigen Tests were sold domestically by a pharmacy in California. These Antigen Tests have not received FDA Emergency Use Authorization, nor have these tests been cleared or approved by FDA for commercial distribution in the U.S.