FDAClass IIMarch 1, 2017

Smith & Nephew Dyonics Saw Blade recall

Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701

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: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485

Product
Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
Recalling firm
Smith & Nephew, Inc.
Quantity
2646
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