Vanguard XP Tibial Tray 75 mm recall
Vanguard XP Tibial Tray 75 mm Item # 195251
Why was Vanguard XP Tibial Tray 75 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 833220 919250 919260 936260 764410 764420 837800 936240 846540 861190 928760 936250 954020 846530 928770 953990 928800 954000 928790 590580 571000 663280 590570 663250 663260 663270 590590 663240 663300 590560 332710 515110 373070 373080 515090 752140 752130 332740 754500
- Product
- Vanguard XP Tibial Tray 75 mm Item # 195251
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 110 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)