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Terminated

Achillon minimally invasive Achilles tendon suture system

FDA Recall Z-1304-04 · Posted 2004-07-31

Recalling FirmWright Medical Technology Inc
Recall StatusTerminated
Product CodeMCZ
Date Initiated2004-07-02
Date Terminated2005-07-05
Product Quantity20 units

Reason for Recall

Lack of sterility assurance

Firm Action

Wright Medical Technology notified its consignees via email and telephone to ensure that the email was received. The consignees asked to return any in-stock recalled product to Wright Medical Technology.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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