FDAClass IIMarch 1, 2017

Smith & Nephew Dyonics Saw Blade recall

Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706

Why was Smith & Nephew Dyonics Saw Blade recalled?

The single use devices are provided sterile and do not have an expiration date 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?

Batch Numbers: 50439354 50393992 50252777 50208023 50171402 50138054 50103142 50066114 576304

Product
Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706
Recalling firm
Smith & Nephew, Inc.
Quantity
1410
Distribution
Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
Recall date
March 1, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls