Z-1215-03

Triton MP-1 Traction Unit

Name: Z-1215-03 Triton MP-1 Traction Unit
Creator: Chattanooga Corp.
Published: 2003-05-30
License: https://open.fda.gov/license/

Chattanooga Corp Inc / initiated 2003-05-30 / Terminated

FDA source

Chattanooga Corp. began a recall of Triton MP-1 Traction Unit on 2003-05-30. The reason FDA records is "Product contains an improper bracket for the transducer". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1215-03
Status: Terminated
Initiated: 2003-05-30
Posted: 2003-09-11
Terminated: 2004-05-07
Recalling firm: Chattanooga Corp Inc
Product: Triton MP-1 Traction Unit
Product code: INW Table, Mechanical
Reason for recall: Product contains an improper bracket for the transducer.
FDA root cause: Other
Action: Recall notification was initiated by telephone on 05/30/2003 to the domestic accounts and via email to the foreign accounts.
Quantity in commerce: 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
Product codes and lots: Model/Catalogue Nos.: 7961 (120 Volt) and 7963 (220 Volt); Serial Numbers: 4231 - 4246, 6806 - 6809, 6815, 6818 ¿ 6819, 6824, 6851, 6856 ¿ 6859, 6863, 6870 ¿ 6873, 6878 ¿ 6919, 6921 ¿ 6958

Product code INW

K801643Class ITritonChattanooga Group, Inc. / cleared 1980-07-28

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)