Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
Class I
- Recalling firm
- Windstone Medical Packaging, Inc.
- Reason for recall
- Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.
- Distribution pattern
- US Nationwide distribution in the state of Arizona.
- State
- MT
- Status
- Ongoing
- Recall number
- Z-2066-2026
- Recall initiated
- April 2, 2026
View on openFDA