Halyard LAVH PACK (Model/Catalog USAR053-11) containing Clearify Visualization System (5303907), UDI/DI 10809160372357, Lot No. 1669869, expiration 4/30/2027 — 40 packs distributed in Texas. The kit is being recalled because a component was subjected to EO sterilization contrary to the manufacturer recommendation, which may have led to the component leaking.
What's being recalled
Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
Recalling firm: AVID Medical, Inc., Toano, VA, United States.
How to identify it
UDI/DI: 10809160372357, Lot No.: 1669869, Expiration Date: 4/30/2027
The hazard
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
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 TX.
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)