PlainRecalls
FDA Devices Moderate Class II Terminated

XP-CR Tibial Tray - Interlok 79 mm Item # 195276

Reported: September 18, 2019 Initiated: August 15, 2019 #Z-2511-2019

Product Description

XP-CR Tibial Tray - Interlok 79 mm Item # 195276

Reason for Recall

The locking bar not fully engaging

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
319 units
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
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
XP-CR Tibial Tray - Interlok 79 mm Item # 195276. Recalled by Zimmer Biomet, Inc.. Units affected: 319 units.
Why was this product recalled?
The locking bar not fully engaging
Which agency issued this recall?
This recall was issued by the FDA Devices on September 18, 2019. Severity: Moderate. Recall number: Z-2511-2019.