FDAClass IIFebruary 6, 2013

TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet recall

TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal fixation devices intended to aid in…

Why was TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet recalled?

Thru hole at the tip of the screw is undersized.

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?

Catalog Number: 909668 Lot Number Identification: 716710

Product
TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal fixation devices intended to aid in…
Recalling firm
Biomet, Inc.
Quantity
44 units distributed
Distribution
Worldwide Distribution - USA including CA, FL, IL, AL, OH, KY, TX , and Internationally to Australia, Columbia, Mexico, Netherlands, and Chile.
Recall date
February 6, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls