Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 83 mm Item # 195277
- Recall date
- August 15, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2512-2019
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- 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
Why it was recalled
The locking bar not fully engaging
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
XP-CR Tibial Tray - Interlok 83 mm Item # 195277
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