Z-0668-03

X-ray, Computed Tomography, Model TSX101A

Name: Z-0668-03 X-ray, Computed Tomography, Model TSX101A
Creator: Toshiba American Med Sys Inc
Published: 2003-01-14
License: https://open.fda.gov/license/

Canon Medical Systems USA, Inc. / initiated 2003-01-14 / Terminated

FDA source

Toshiba American Med Sys Inc began a recall of X-ray, Computed Tomography, Model TSX101A on 2003-01-14. The reason FDA records is "Misassembly can cause fire". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0668-03
Status: Terminated
Initiated: 2003-01-14
Posted: 2003-03-21
Terminated: 2005-06-17
Recalling firm: Canon Medical Systems USA, Inc.
Product: X-ray, Computed Tomography, Model TSX101A
Product code: JAK System, X-Ray, Tomography, Computed
Reason for recall: Misassembly can cause fire.
FDA root cause: Other
Action: Letters to consignees were sent 2/12 and 2/13/2003. The letters inform customers that Toshiba America Medical Systems would be making appointments to check and service their machine.
Quantity in commerce: 68
Distribution: Nationwide.
Product codes and lots: None.

Product code JAK

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)