Synthes 4.5 mm LCP Curved Condylar Plate Intended for recall
Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
Why was Synthes 4.5 mm LCP Curved Condylar Plate Intended for recalled?
The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight Condylar Plate is etched with a Curved Condylar Plate part number.
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?
Part No. 02.001.324, lot no. 6900823
- Product
- Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
- Recalling firm
- Synthes USA HQ, Inc.
- Quantity
- 13
- Distribution
- Worldwide Distribution - USA including ID, FL, TN, NY, LA and Internationally to Canada.
- Recall date
- December 4, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)