FDA recall record

Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701 recall — FDA Z-1239-2017

The single use devices are provided sterile and do not have an expiration date on the label.

Class IIclassification
Z-1239-2017official record ID
Mar 1, 2017report date

Recall record at a glance

Official recordZ-1239-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSmith & Nephew, Inc.
Report dateMar 1, 2017
Recall initiation dateFeb 2, 2017
Quantity2646
LocationMemphis, TN, United States

Official product description

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

Why the product was recalled

The single use devices are provided sterile and do not have an expiration date on the label.

Distribution information

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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