Genius Knee Cemented Tibial Component Product Usage recall
Genius Knee Cemented Tibial Component Product Usage: Knee replacement component
Why was Genius Knee Cemented Tibial Component Product Usage recalled?
Product mix up
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?
UDI # 09348215020309 Device Model # 121-07-4004 Lot # 77A3F
- Product
- Genius Knee Cemented Tibial Component Product Usage: Knee replacement component
- Recalling firm
- Signature Orthopedics Pty Limited
- Quantity
- 10
- Distribution
- US Nationwide Distribution in the states of FL, NY, and TN
- Recall date
- February 20, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)