FDA Device recall Z-0155-2014
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process
- FDA Device
- Class III
- terminated
- Published 2013-11-13
On 2013-11-13 the FDA classified a Class III recall of ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process by Trumpf Medical Systems, citing an odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0155-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-07-24 |
| Published | 2013-11-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Trumpf Medical Systems |
| Distribution | NJ |
Product
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.
Reason
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Identifiers
| code_info | Item No. 1275499, Serial No. 100711351 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0155-2014%22
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