XP-CR Tibial Tray - Interlok 73mm recall
XP-CR Tibial Tray - Interlok 73mm Item # 195274
Why was XP-CR Tibial Tray - Interlok 73mm recalled?
The locking bar not fully engaging
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Number 553880 590760 663690 553880R 590750 663670 262430 513080 663720 513080R 472990 938180 578980 090230 159280 676320 258090 043920 066220 206850 322110 352860 841550 917740 966760 283230 374810 283240 996010 352850 352850R 429270 851300 383710 041300 585600 076010 469520 578970 599150 600800 600800R 279040 450360 672600 374090 943410 712580 121150 018040 821330 121140 199740 218670 717190 308100 308110 502840 513070 571040 502840R 513070R 571040R
- Product
- XP-CR Tibial Tray - Interlok 73mm Item # 195274
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 327 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
- Recall date
- September 18, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)