FDAClass IIMarch 7, 2018

The 2nd Assist Knee Positioner recall

The 2nd Assist Knee Positioner

Why was The 2nd Assist Knee Positioner recalled?

Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.

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?

Item# 740026

Product
The 2nd Assist Knee Positioner
Recalling firm
Zimmer Biomet, Inc.
Quantity
38,879 units
Distribution
Nationally
Recall date
March 7, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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