Atlas FDA

Dynasty Trial Shell 62mm Group G, REF 3300-GG62, Rx only, Non-Sterile, 1 each, Wright Medical Technology, Inc., 5677 Air

FDA device recall Z-2215-2008 · posted 2008-09-17 · Terminated

Recall details

Recalling firm
Wright Medical Technology Inc
Reason for recall
Trials are 2.5mm larger than marked.
Action taken
The firm initiated their recall on May 20, 2008 by issuing a Field Notice to their distributors and followed with telephone calls on May 21 and 22, 2008 requesting the return of the products. The firm then issued letters to their distributors on June 4, 2008 explaining the problem and requesting return of the product from their inventory and from their consignees. The letter included a "fax back" response page to ensure the receipt of the notice. The hospitals were notified of the recall also on June 4, 2008 by means of letters, delivered via Fed Ex, addressed to Hospital Administrators, Risk Managers, and Orthopaedic Department Managers.
Root cause
Component change control
Status
Terminated
Product code
LXH
Quantity affected
128 units
Distribution
Worldwide Distribution --- including USA and Canada.
Date initiated
2008-05-20
Date posted
2008-09-17
Date terminated
2009-01-25
Location
Arlington, TN

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