FDAClass IIOctober 3, 2018

Biomet Sports Medii cine Juggerknot Long Flex Drill Bit recall

Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for…

Why was Biomet Sports Medii cine Juggerknot Long Flex Drill Bit recalled?

Expiration date incorrectly listed on the label

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?

Lot Numbers: 053940, 545740, 067490, 664610, 165770, 676180, 165830, 688250, 415590, 860050

Product
Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for…
Recalling firm
Zimmer Biomet, Inc.
Quantity
217 units
Distribution
AZ CO FL FL GA LA MA MA MO NY SC TX
Recall date
October 3, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls