XP-XP Tibial Tray - Interlok 87 mm recall
XP-XP Tibial Tray - Interlok 87 mm Item # 195760
Why was XP-XP Tibial Tray - Interlok 87 mm 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 790970 984810 984820 202000R 664250R 664280R 685040 885800 716010 873630 903460 960480 960500 201990 202000 664250 664280 400690 394670 394710 293220 183680 394330
- Product
- XP-XP Tibial Tray - Interlok 87 mm Item # 195760
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 90 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)