Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2066-2026 — Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F

U.S. FDA — Device Enforcement · United States · 2026-04-02 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2066-2026
Date of alert
2026-04-02
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Windstone Medical Packaging, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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