ATTUNE Revision CRS Femoral LT SZ 5 Cemented recall
ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee
Why was ATTUNE Revision CRS Femoral LT SZ 5 Cemented recalled?
There may be burrs on the extraction hole threads.
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 HC1179, GTIN Number 10603295042181; Lot Number HC1183, GTIN Number 10603295042181
- Product
- ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee
- Recalling firm
- DePuy Orthopaedics, Inc.
- Quantity
- 2 units
- Distribution
- The products were distributed to the following US states: FL, MO, and PA.
- Recall date
- May 16, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)