Avid Medical, Inc.: Orthopedic Tray

Recall Summary AVID Medical is recalling Halyard Eye Bag Pack kits (Kit Code: UIEB48-01) distributed nationwide because some sealed pouches were shipped without going through the required sterilization process. These orthopedic trays were distributed across all U.S. states and Washington, DC. This is classified as a Class I recall, the most serious type.

Recalling firm
AVID Medical, Inc.
Product
Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
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/2da6a8f4-f3bf-4db8-8740-2818bb2f356a