United StatesThe Custom Convenience Kit containing Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes), Angio Pack part numbers AMS6908E (UDI‑DI B098AMS6908E0, lot 214875) and AMS6908F (UDI‑DI B098AMS6908F0, lots 215436, 225001, 226706, 234088) distributed in Arizona is affected. It was recalled because the rotating adapter can unwind during use, which may cause a loose connection or full disconnection between syringe and manifold and could result in biohazard exposure, blood loss, infection, or air embolism.
What's being recalled
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., Billings, MT, United States.
How to identify it
Pack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088
The 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.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the state of Arizona.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)