- Recalling firm
- Zimmer, Inc.
- Reason for recall
- Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
- Affected products (lot / model / serial)
- Lot Code: Model No. 110040476 ; UDI-DI (01)00889024682047(17)350531(10)097492 ; Lot Number 097492
- Units affected
- 13 units
- Distribution pattern
- US Nationwide distribution.
- Firm location
- Warsaw, IN, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2531-2026
- Recall initiated
- May 20, 2026
- FDA classification date
- June 23, 2026
- FDA report date
- July 1, 2026
- FDA event ID
- 99045
- Last updated on HTM Vibe
- July 23, 2026