ORBIT PT — Class III medical device recall Z-0155-2014
Terminated recall by Trumpf Medical Systems, reported 2013-11-13, distributed in NJ. An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller col
| Recall number | Z-0155-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trumpf Medical Systems, Charleston, SC, United States |
| Recall initiated | 2013-07-24 |
| Classified | 2013-11-05 |
| Reported by FDA | 2013-11-13 |
| Terminated | 2014-06-03 |
| Distributed | NJ |
| Serial numbers | 100711351 |
| Model numbers | 1275499 |
Product
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.
Reason for recall
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0155-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.