United StatesMedical Action Industries Inc. Pack Cath BHH (REF BHCA49K, Sterile EO, Rx Only, 5/Case), UDI 20809160490294, lots 342509, 346066, 338434, 339423, 337365, 335489, 336189 and 336789 — 2,030 kits distributed in Arizona — are affected. The kits were recalled because a syringe’s rotating adapter may unwind during use, resulting in a loose connection or full disconnection between the syringe and the manifold.
What's being recalled
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Recalling firm: Medical Action Industries, Inc. 306, Arden, NC, United States.
How to identify it
UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
The hazard
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
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 distribution to state of: AZ OUS: None
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)