Vanguard XP Tibial Tray 69 mm recall
Vanguard XP Tibial Tray 69 mm Item # 195248
Why was Vanguard XP Tibial Tray 69 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 117720 332660 373010 373000 514970 515000 372990 039210 112980 113000 112990 202920 303370 303380 590480 660400 660410 584210 590490 833180 752040 752050 752560 752060 919220 928860 754470 764360 837750 764350 846490 861180 881480 881490 928870 846500 881460 984370 984380 984360 837760 570940
- Product
- Vanguard XP Tibial Tray 69 mm Item # 195248
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 123 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)