AVID Medical, Inc. 2026-07-29 Health serious FDA
Health · FDA · Recall #FDA-Z-2772-2026
Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience… Recall
Issued July 29, 2026 · AVID Medical, Inc.
In July 2026, AVID Medical, Inc. recalled the Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience…, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
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 you should do
- 1 Stop using Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact AVID Medical, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- AVID Medical, Inc.
- Category
- Health
- Recall date
- July 29, 2026
- Units affected
- Not reported
- Sold at
- U.S. Nationwide distribution in the state of California.
- Recall number
- FDA-Z-2772-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- AVID Medical, Inc. has 10 recalls in our database, including 1 rated Critical.
- We're tracking 3,707 Health recalls in our database.
- This is the 487th Health recall we've logged in 2026.