FDA recall Z-2525-2019

Zimmer Biomet, Inc. · Class II · device

Product

XP-XP Tibial Tray - Interlok 65 mm Item # 195752

Reason for recall

The locking bar not fully engaging

Distribution

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

Key facts

Status
Terminated
Initiation date
2019-08-15
Report date
2019-09-18
Termination date
2021-04-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2525-2019