Vanguard XP Tibial Tray 67 mm recall
Vanguard XP Tibial Tray 67 mm Item # 195247
Why was Vanguard XP Tibial Tray 67 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 332640 833160 514940 372960 372970 514920 752020 752030 919210 764330 754460 884550 837740 764340 861170 884360 887950 935780 935800 953910 968990 953950 928850 936190 953930 953940 861160 663120 660390 663080 663110 584200
- Product
- Vanguard XP Tibial Tray 67 mm Item # 195247
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 74 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)