Recall Z-0141-2015— Trumpf Medical Systems, Inc.
Class II · Terminated
Class II FDA medical device recall by Trumpf Medical Systems, Inc., initiated 2014-10-09, terminated 2016-03-23. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Trumpf Medical Systems, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-10-09
- Terminated
- 2016-03-23
- Firm location
- Charleston, SC, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.