Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument recall
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Why was Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument recalled?
The manufacturer informed the recalling firm of a potential laser marking error in size identification on two Columbus 4-IN-1 Femoral Cutting Guide Instruments. The guides are correctly dimensioned, but the laser markings have been incorrectly etched.
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?
NQ083R
- Product
- Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
- Recalling firm
- Aesculap, Inc.
- Quantity
- 2
- Distribution
- Within the US, product was distributed to PA and TN.
- Recall date
- October 24, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)