FDAClass IISeptember 18, 2019

XP- CR Tibial Tray- Interlok 59mm recall

XP- CR Tibial Tray- Interlok 59mm Item # 195268

Why was XP- CR Tibial Tray- Interlok 59mm 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 004960 262370 130580 004970 130630 130550 130610 130560 130570 004950 130590 279210

Product
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Recalling firm
Zimmer Biomet, Inc.
Quantity
45 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)
Open FDA enforcement record Latest recalls