Vanguard XP Tibial Tray 71 mm recall
Vanguard XP Tibial Tray 71 mm Item # 195249
Why was Vanguard XP Tibial Tray 71 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 584220 590500 590510 663160 663180 663170 660420 117730 332670 833200 373020 373040 373030 515030 515020 515040 752090 752070 752080 919240 919230 846510 764370 764380 837780 754480 837770 861200 881500 881510 984430 984400 039230 052240 039240 881530 984390 039220 984420 052260 984410 090340 570960
- Product
- Vanguard XP Tibial Tray 71 mm Item # 195249
- Recalling firm
- Zimmer Biomet, Inc.
- 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)