Z-2408-2026 Class II Ongoing
FDA device recall Z-2408-2026 was initiated by AVID Medical, Inc. on April 30, 2026 and is designated Class II. Reason for recall: Inadvertent distribution of sealed pouches that had not undergone validated sterilization. The recall status is ongoing. Affected quantity: 224 kits.
Recall Details
- Product Type
- Devices
- Report Date
- June 17, 2026
- Initiation Date
- April 30, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 224 kits
Product Description
Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Reason for Recall
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Distribution Pattern
US Nationwide distribution in the state of Iowa.
Code Information
Kit Code: AMTS70-01. UDI-DI: 10809160469972. Lot Number: AMTS70-01. Expiration Date: 9/2/2028.