Z-2513-2019 Class II Terminated
FDA device recall Z-2513-2019 was initiated by Zimmer Biomet, Inc. on August 15, 2019 and is designated Class II. Reason for recall: The locking bar not fully engaging The recall status is terminated (terminated April 16, 2021). Affected quantity: 78 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 18, 2019
- Initiation Date
- August 15, 2019
- Termination Date
- April 16, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 78 units
Product Description
XP-CR Tibial Tray - Interlok 87 mm Item # 195278
Reason for Recall
The locking bar not fully engaging
Distribution Pattern
State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Code Information
Lot Number 966230 262470 587200 274370 274360 274380 274420 715690 274420R 715690R 393650 279080 394490 821380 903430 943440 422480 512580