Vanguard XP Tibial Tray 73 mm recall
Vanguard XP Tibial Tray 73 mm Item # 195250
Why was Vanguard XP Tibial Tray 73 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 590540 590530 590520 663190 590550 663200 907710 117740 332690 833210 752580 373050 373060 515050 752120 515070 752100 752110 754490 764390 861210 837790 936210 764400 846520 928890 907690 936220 936230 954050 928880 936200 954030 907700 063000 062990 570980 584230
- Product
- Vanguard XP Tibial Tray 73 mm Item # 195250
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 84 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)