Aesculap Columbus Revision CoCr 15mm distal and recall
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Why was Aesculap Columbus Revision CoCr 15mm distal and recalled?
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
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: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597
- Product
- Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
- Recalling firm
- Aesculap, Inc.
- Quantity
- 24
- Distribution
- Distributed in FL and MD.
- Recall date
- December 25, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)