FDAClass IIMarch 23, 2016

Battery Pack KLS-SD-1000 Single recall: Particulate Matter

Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

Why was Battery Pack KLS-SD-1000 Single recalled?

The sterile battery may contain particulates within the sterile package.

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 509567, K055R

Product
Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
Recalling firm
Pro-Dex Inc
Quantity
1995 total
Distribution
Distributed in FL.
Recall date
March 23, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
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