Bayer Medical Care, Inc.: Injector And Syringe, Angiographic
- Recalling firm
- Bayer Medical Care, Inc.
- Product
- MEDRAD Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;
- Reason
- Some devices may not have been properly sterilized due to a manufacturing sterilization issue.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-07-31
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/f0e2122c-77b4-4085-af41-75c28c353c55