Z-0987-03

3D Ceiling Suspension

Name: Z-0987-03 3D Ceiling Suspension
Creator: Siemens Medical Solutions USA, Inc
Published: 2003-04-15
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2003-04-15 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of 3D Ceiling Suspension on 2003-04-15. The reason FDA records is "the back up safety catch may not function properly". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0987-03
Status: Terminated
Initiated: 2003-04-15
Posted: 2003-07-10
Terminated: 2005-04-11
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: 3D Ceiling Suspension
Product code: IZF System, X-Ray, Tomographic
Reason for recall: the back up safety catch may not function properly
FDA root cause: Other
Action: Letters dated 4/15/03 and 4/23/03 were issued to the accounts along with instructions on how to fix the problem.
Quantity in commerce: 3504 units
Distribution: The product was shipped nationwide to medical facilities.
Product codes and lots: all serial numbers

Product code IZF

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)