Avid Medical, Inc.: Orthopedic Tray
Recall Summary AVID Medical is recalling Halyard Drape Pack orthopedic trays (Kit Code LMDP36-01) distributed nationwide because some sealed pouches were shipped without completing the required sterilization process. This is a Class I recall, the most serious classification. The affected products were distributed across all U.S. states and Washington, D.C.
- Recalling firm
- AVID Medical, Inc.
- Product
- Halyard, Drape Pack. Kit Code: LMDP36-01.
- 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/a06626ef-324c-43b1-80ef-0c851abcaa74