Home/Recalls/FDA-Z-2066-2026
FDA DevicesClass I

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

Published: May 20, 2026Recall ID: Z-2066-2026Category: devicesCountry: US
US
Medical DeviceFDA DevicesUSUS

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

Recalling Firm: Windstone Medical Packaging, Inc.

Reason for Recall / 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.

Product Description & Identification

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 with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F

Additional Source Details

FieldValue
CityBillings
StateMT
Event id98741
Address 11602 4th Ave N
Code infoPack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088
Postal code59101-1521
Report date20260520
Product typeDevices
Product quantity150 kits (US only)
Reason for recallAffected 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260402
Initial firm notificationE-Mail
Center classification date20260508

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Overview

  • Recalling FirmWindstone Medical Packaging, Inc.
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS Nationwide distribution in the state of Arizona.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: Windstone Medical Packaging, Inc. - Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F

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