XP-XP Tibial Tray - Interlok 59 mm recall
XP-XP Tibial Tray - Interlok 59 mm Item # 195750
Why was XP-XP Tibial Tray - Interlok 59 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 206540 057180 206590 206580 206550 030800 206560 457940 457880 457930 457970 457950
- Product
- XP-XP Tibial Tray - Interlok 59 mm Item # 195750
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 50 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)