Atlas FDA

Triton MP-1 Traction Unit

FDA device recall Z-1215-03 · posted 2003-09-11 · Terminated

Recall details

Recalling firm
Chattanooga Corp.
Reason for recall
Product contains an improper bracket for the transducer.
Action taken
Recall notification 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
INW
Quantity affected
96
Distribution
Nationwide. TX, CO, MD, VA, FL, PA, NJ, NY, IN, OH, MI, MO, AL, NV, IL, CA, NM, AR, LA, NE, WA, NC, A, NH, and OK
Date initiated
2003-05-30
Date posted
2003-09-11
Date terminated
2004-05-07
Location
Hixson, TN

Monitor recalls programmatically

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

Related 510(k) clearances

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