FDA Device recall Z-0141-2015
TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthe…
- FDA Device
- Class II
- terminated
- Published 2014-11-05
On 2014-11-05 the FDA classified a Class II recall of TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthe… by Trumpf Medical Systems, citing unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0141-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-09 |
| Published | 2014-11-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Trumpf Medical Systems |
| Distribution | US |
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
Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.
Identifiers
| code_info | TITAN Operating Tables: 1465166, 1228073, 1397903, 4544260. |
|---|
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-0141-2015%22
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