FDAClass IIDecember 4, 2013

Synthes 4.5MM TI VA-LCP CRVD Condylar recall

Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER is used for buttressing…

Why was Synthes 4.5MM TI VA-LCP CRVD Condylar recalled?

A plate was inadvertently released to a sales consultant that was restricted for sale.

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 04.124.406S, lot 3771678.

Product
Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER is used for buttressing…
Recalling firm
Synthes USA HQ, Inc.
Quantity
1
Distribution
US Distribution in Colorado.
Recall date
December 4, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls