Avid Medical, Inc.: Orthopedic Tray
Recall Summary AVID Medical is recalling Halyard Pain Pack orthopedic kits (Kit Code AMPK48-01) distributed nationwide because some sealed pouches were shipped without undergoing the required sterilization process. This is a serious recall because non-sterile surgical instruments can pose infection risks. The affected kits were distributed across all U.S. states and Washington, D.C.
- Recalling firm
- AVID Medical, Inc.
- Product
- Halyard, Pain Pack. Kit Code: AMPK48-01.
- Reason
- Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-30
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of Iowa.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/343d58b0-2ab6-420f-a0e0-30efd4a8dfa5