Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
Philips is recalling certain Azurion 7 B20 X-ray imaging systems because the wired foot switch may fail to start X-ray imaging or may cause it to work intermittently. The recall affects three specific system models distributed nationwide in the U.S. and internationally across numerous countries. This is classified as a Class II recall.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Product
- Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
- Reason
- Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-03-03
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Domestic: Nationwide Distribution; International: Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Botswana, Brazil, Brunei Darussal, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China,...
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/ed00855c-5fea-42ef-bf1e-7585d1b169bc