FDAClass I · Medical device · Recalled May 20, 2026

Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit recall — Windstone Medical Packaging, Inc.

Hazard: 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.

Class I: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2066-2026
Brand: Windstone Medical Packaging
Classification: Class I
Units affected: 150 kits (US only)
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F

Affected products

Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit

Companies & origin

Recalling firm location: Billings, MT, United States
Firm address: 1602 4th Ave N, 59101-1521

Identifying details (verbatim from the notice)

Product codes / lots: Pack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088
Distribution: US Nationwide distribution in the state of Arizona.
Firm notified the public via: E-Mail
FDA event ID: 98741
Recall initiated: April 2, 2026
FDA classified: May 8, 2026
FDA report date: May 20, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 3:00 AM UTC.

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