AVID Medical, Inc. 2024-11-20 Health serious FDA
Health · FDA · Recall #FDA-Z-0454-2025
Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02 Recall
Issued November 20, 2024 · AVID Medical, Inc.
In November 2024, AVID Medical, Inc. recalled the Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
What you should do
- 1 Stop using Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02 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
- November 20, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-0454-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- AVID Medical, Inc. has 9 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.