Atlas FDA

Triton T-700 Traction Unit,

FDA device recall Z-1210-03 · posted 2003-09-11 · Terminated

Recall details

Recalling firm
Chattanooga Corp.
Reason for recall
Product contains an improper bracket for the transducer.
Action taken
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
Status
Terminated
Product code
ITF
Quantity affected
18 units
Distribution
IL, CA, TX, OH, FL, LA, WA, NC and DC
Date initiated
2003-05-30
Date posted
2003-09-11
Date terminated
2004-05-07
Location
Hixson, TN

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Related 510(k) clearances

RecordFirmDate
TRITON (K801643)Chattanooga Group, Inc.1980-07-28