Atlas FDA

Stem Trial, Triathlon Revision Instruments; Non-Sterile; 150 mm length Catalog Numbers: 5566-T-009, 5566-T-010, 5566-T-0

FDA device recall Z-2158-2008 · posted 2008-08-23 · Terminated

Recall details

Recalling firm
Stryker Howmedica Osteonics Corp.
Reason for recall
Triathlon TS Stems Trails may crack, potentially causing fragments of the plastic handle to fragment and break off completely.
Action taken
Urgent Product Recall notification letters were sent to all Stryker Branch/Agency Manager/Quality contacts on May 14, 2008 via Federal Express. The letter requests that consignees examine their inventory and hospital consignment locations to identify the product; and retrieve all affected product lots and return it to their branch or agency warehouse for reconciliation. The letter also states that a Stryker Orthopaedics Customer Service rep should be contacted for alternative products available.
Root cause
Process control
Status
Terminated
Product code
HWT
Quantity affected
Catalog 5566 T-009 to 025: 2625 US, 239 international
Distribution
Worldwide Distribution --- including USA and countries of Australia, Canada, Sweden, Germany, Spain, Portugal, United Kingdom.
Date initiated
2008-05-14
Date posted
2008-08-23
Date terminated
2010-01-26
Location
Mahwah, NJ

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.