Z-0396-2012

OR table TITAN T, Surgical Table. Surgical bed with Orthopedic Accessories

Name: Z-0396-2012 OR table TITAN T, Surgical Table. Surgical bed with Orthopedic Accessories
Creator: Trumpf Medical Systems, Inc.
Published: 2011-01-21
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2011-01-21 / Terminated / root cause: design

FDA source

Trumpf Medical Systems, Inc. began a recall of OR table TITAN T, Surgical Table. Surgical bed with Orthopedic Accessories on 2011-01-21. The reason FDA records is "Product is being recalled due to unintended movement on the Titan Tables". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0396-2012
Status: Terminated
Initiated: 2011-01-21
Posted: 2012-01-11
Terminated: 2012-08-13
Recalling firm: Hill-Rom Inc.
Product: OR table TITAN T, Surgical Table. Surgical bed with Orthopedic Accessories.
Product code: FQO Table, Operating-Room, Ac-Powered
Reason for recall: Product is being recalled due to unintended movement on the Titan Tables.
Root cause tag: design
FDA root cause: Device Design
Action: Trumpf Medical Systems sent an initial notification to customers dated January 24, 2011. A subsequent "URGENT SAFETY NOTICE-UPDATE" letter dated May 26, 2011 was sent to all affected customers. The letter described the product, problem, and actions to be taken by the customers. A Corrective Action Plan includes a software update to be installed by a Trumpf Technical Service Representative. Contact Technical Service at 888-474-9359 for questions regarding this notice.
Quantity in commerce: see line 1.
Distribution: Worldwide Distribution.
Product codes and lots: Material number: 197903, All Serial numbers.

Product code FQO

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 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)