FDAClass IIFebruary 8, 2017

Cannulated Drill bit 2.0mm and 2.6 mm recall

Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.

Why was Cannulated Drill bit 2.0mm and 2.6 mm recalled?

The product is being recalled due to incidence and reports of the product breaking during surgery.

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?

Device Listing: D267957

Product
Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.
Recalling firm
Flower Orthopedics Corporation
Quantity
N/A
Distribution
Distributed throughout the United States
Recall date
February 8, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
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