- Recalling firm
- Windstone Medical Packaging, Inc.
- 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.
- Affected products (lot / model / serial)
- Pack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088
- Units affected
- 150 kits (US only)
- Distribution pattern
- US Nationwide distribution in the state of Arizona.
- Firm location
- Billings, MT, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2066-2026
- Recall initiated
- April 2, 2026
- FDA classification date
- May 8, 2026
- FDA report date
- May 20, 2026
- FDA event ID
- 98741
- Last updated on HTM Vibe
- July 24, 2026