FDAClass IISeptember 18, 2019

Vanguard XP Tibial Tray 83 mm recall

Vanguard XP Tibial Tray 83 mm Item # 195253

Why was Vanguard XP Tibial Tray 83 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 332760 752520 515140 754520 063070 072460 072440 072510 663350 663360 833240 919270 764460 846570 764450 837820 861240 915690 915700

Product
Vanguard XP Tibial Tray 83 mm Item # 195253
Recalling firm
Zimmer Biomet, Inc.
Quantity
49 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