TITAN Operating Room Table Patient positioning during surgery — Class II medical device recall Z-0141-2015
Terminated recall by Trumpf Medical Systems, Inc., reported 2014-11-05, distributed nationwide. Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.
| Recall number | Z-0141-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trumpf Medical Systems, Inc., Charleston, SC, United States |
| Recall initiated | 2014-10-09 |
| Classified | 2014-10-27 |
| Reported by FDA | 2014-11-05 |
| Terminated | 2016-03-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 184 units |
Product
TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
Reason for recall
Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.
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-0141-2015. 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.