Vanguard XP Tibial Tray 79 mm recall
Vanguard XP Tibial Tray 79 mm Item # 195252
Why was Vanguard XP Tibial Tray 79 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 332750 833230 515120 752550 515130 373090 919280 754510 764430 764440 861230 837810 846560 907730 928810 907720 907740 969000 969010 590620 590600 663320 663330 663340 590610 571010 663310
- Product
- Vanguard XP Tibial Tray 79 mm Item # 195252
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 99 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)