# FDA recall Z-2066-2026

> **Windstone Medical Packaging, Inc.** · Class I · device recall initiated 2026-04-02.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-2066-2026
- **Recalling firm:** Windstone Medical Packaging, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-02
- **Report date:** 2026-05-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Billings, MT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2066-2026

## Citation

> MORVS. FDA recall Z-2066-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-2066-2026. Source: US FDA. Licensed CC0.

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