Z-0155-2014 Class III Terminated
FDA device recall Z-0155-2014 was initiated by Trumpf Medical Systems on Jul 24, 2013 and is designated Class III. Reason for recall: An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column. The recall status is terminated (terminated Jun 3, 2014). Affected quantity: One.
Recall details
- Product Type
- Devices
- Report Date
- Nov 13, 2013
- Initiation Date
- Jul 24, 2013
- Termination Date
- Jun 3, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- One
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.
Distribution pattern
US Distribution: NJ only.
Code information
Item No. 1275499, Serial No. 100711351
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0155-2014
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026