Atlas FDA

Achillon minimally invasive Achilles tendon suture system

FDA device recall Z-1304-04 · posted 2004-07-31 · Terminated

Recall details

Recalling firm
Wright Medical Technology Inc
Reason for recall
Lack of sterility assurance
Action taken
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
Status
Terminated
Product code
MCZ
Quantity affected
20 units
Distribution
Nationwide
Date initiated
2004-07-02
Date posted
2004-07-31
Date terminated
2005-07-05
Location
Arlington, TN

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