TemporaryFDAOngoing
Can cause harm that is usually temporary.
MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;
Check the device or its packaging for
Catalog number: FLEXS-150-QFT; UDI-DI: 00616258022895; Affected material number: 87078825; Affected batch number: 8688750;
- Why
- Some devices may not have been properly sterilized due to a manufacturing sterilization issue.
- Distributed
- US Nationwide distribution.
- Company
- Bayer Medical Care, Inc.
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-3147-2026 · retrieved 11 September 2026
Read the official notice