Medical Device Recall: Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
Windstone Medical Packaging, Inc. · April 2, 2026
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
US Nationwide distribution in the state of Arizona.
States Affected
NATIONWIDE
Quantity Affected
150 kits (US only)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2066-2026
Status: ongoing
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