FDAFDA · Food and drugs·Recall number Z-2527-2019
XP-XP Tibial Tray - Interlok 59 mm Item # 195750
Published September 18, 2019 · Recall initiated: August 15, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The locking bar not fully engaging
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Zimmer Biomet, Inc.
- Distributor
- 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
- Lot
- Lot Number 206540 057180 206590 206580 206550 030800 206560 457940 457880 457930 457970 457950
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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