Triton T-700 Traction Unit,
FDA Recall Z-1210-03 · Posted 2003-09-11
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Recalling FirmChattanooga Corp.
Recall StatusTerminated
Product CodeITF
Date Initiated2003-05-30
Date Terminated2004-05-07
Product Quantity18 units
Reason for Recall
Product contains an improper bracket for the transducer.
Firm Action
Notification of the manufacturing defect and recall was initiated by telephone on 05/30/2003 to the domestic accounts and via email to the foreign accounts.
Root Cause
Other
Distribution Pattern
IL, CA, TX, OH, FL, LA, WA, NC and DC
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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