Z-0986-05

Magnetic Resonance Imaging Systems; Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart...

Name: Z-0986-05 Magnetic Resonance Imaging Systems; Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart...
Creator: Toshiba American Med Sys Inc
Published: 2005-05-25
License: https://open.fda.gov/license/

Canon Medical Systems USA, Inc. / initiated 2005-05-25 / Terminated

FDA source

Toshiba American Med Sys Inc began a recall of Magnetic Resonance Imaging Systems; Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart VANTAGE on 2005-05-25. The reason FDA records is "Patient information A is displayed with images for patient B". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0986-05
Status: Terminated
Initiated: 2005-05-25
Posted: 2005-07-13
Terminated: 2012-04-05
Recalling firm: Canon Medical Systems USA, Inc.
Product: Magnetic Resonance Imaging Systems; Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart VANTAGE.
Product code: LNH System, Nuclear Magnetic Resonance Imaging
Reason for recall: Patient information A is displayed with images for patient B.
FDA root cause: Other
Action: Firm will have technicians correct each unit by visit. Instructions to them have issued.
Quantity in commerce: 102
Distribution: Nationwide.
Product codes and lots: All.

Product code LNH

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)