- Recalling firm
- Zimmer, Inc.
- Reason for recall
- Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
- Affected products (lot / model / serial)
- Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947
- Units affected
- 12
- Distribution pattern
- Refer to the attached ZFA 2026-00088_Initial Consignee List and ZFA 2026-00088_Initial Distribution History containing the distribution and the identification of the affected consignees.
- Firm location
- Warsaw, IN, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2578-2026
- Recall initiated
- May 11, 2026
- FDA classification date
- June 24, 2026
- FDA report date
- July 1, 2026
- FDA event ID
- 99073
- Last updated on HTM Vibe
- July 23, 2026