FDAClass IISeptember 21, 2016

Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar recall

Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar Nail System is intended to provide strong and stable internal fixation with minimal soft tissue…

Why was Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar recalled?

Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.

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 18220930S and Lot Code K836729

Product
Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar Nail System is intended to provide strong and stable internal fixation with minimal soft tissue…
Recalling firm
Stryker Howmedica Osteonics Corp.
Quantity
1 unit in total
Distribution
US distribution to state of: CA.
Recall date
September 21, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls