- 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. 110040241 ; UDI-DI (01)00889024681941(17)350602(10)099463 ; Lot Number 099463 Model No. 110040241 ; UDI-DI (01)00889024681941(17)350531(10)099464 ; Lot Number 099464 Model No. 110040241 ; UDI-DI (01)00889024681941(17)350812(10)099465 ; Lot Number 099465 Model No. 110040241 ; UDI-DI (01)00889024681941(17)350707(10)099467 ; Lot Number 099467
- Units affected
- 435 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-2528-2026
- 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