United StatesThe Halyard STANDARD LINE INSERTION PACK convenience kit (Model/Catalog PVHM234-01, UDI‑DI 10809160416761; lots 1597314 exp. 8/31/2026 and 1599022 exp. 5/31/2026) sold by AVID Medical, Inc. in California (112 kits) is affected. It was recalled because defects in the silicone seal may cause “doming” from improper sealing, potentially resulting in fluid occlusion or leakage.
What's being recalled
Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
Recalling firm: AVID Medical, Inc., Toano, VA, United States.
How to identify it
Model/Catalog Number: PVHM234-01. UDI-DI: 10809160416761. Lot Numbers (Expiration date): 1597314 (8/31/2026), 1599022 (5/31/2026).
The hazard
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
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
U.S. Nationwide distribution in the state of California.
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)