ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 recall
ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number…
Why was ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 recalled?
May have adhesive residue on the posterior surface of the femoral augment, if undetected prior to implantation, soft tissue irritation and/or infection may occur.
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?
Lots: JH9651, JH9649 GTIN: 10603295383178
- Product
- ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number…
- Recalling firm
- DePuy Orthopaedics, Inc.
- Quantity
- 6 units
- Distribution
- US Nationwide distribution in the states of TN, TX.
- Recall date
- February 16, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)