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Terminated

Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702

FDA Recall Z-1240-2017 · Posted None

Recalling FirmSmith & Nephew, Inc.
Recall StatusTerminated
Product CodeHAB
Date Initiated2017-02-02
Date Terminated2019-09-20
Product Quantity2496

Reason for Recall

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

Firm Action

Smith & Nephew, Inc. initiated recall by letter on 2/2/17 advising of the problem, requesting inspection of inventory and return of product. Contact Smith & Nephews Field Actions Department via email at [email protected] or fax +1-901-566-7975 to return.

Root Cause

Labeling Change Control

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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