Recall Z-0155-2014— Trumpf Medical Systems
Class III · Terminated
Class III FDA medical device recall by Trumpf Medical Systems, initiated 2013-07-24, terminated 2014-06-03. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Trumpf Medical Systems
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2013-07-24
- Terminated
- 2014-06-03
- Firm location
- Charleston, SC, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.