FDAClass IIJune 8, 2022

Ratcheting Screwdriver Handle recall

Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit

Why was Ratcheting Screwdriver Handle recalled?

The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

Model: MWJ128, Ratcheting Screwdriver Handle, all lot codes

Product
Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit
Recalling firm
Tornier, Inc
Quantity
1066 units
Distribution
US Nationwide distribution.
Recall date
June 8, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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