Fresh Recalls

FDAClass I · Medical device · Recall Z-2066-2026 · Recalled May 20, 2026

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

Agency report date: May 20, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit
Company / brand
Windstone Medical Packaging
Lot / serial / date codes
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.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit

3. Open the official notice or contact

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

Affected products

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
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved August 18, 2026 at 6:00 PM UTC.

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