Z-0141-2015 Class II Terminated
FDA device recall Z-0141-2015 was initiated by Trumpf Medical Systems, Inc. on Oct 9, 2014 and is designated Class II. Reason for recall: Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes. The recall status is terminated (terminated Mar 23, 2016). Affected quantity: 184 units.
Recall details
- Product Type
- Devices
- Report Date
- Nov 5, 2014
- Initiation Date
- Oct 9, 2014
- Termination Date
- Mar 23, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 184 units
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.
Distribution pattern
Worldwide Disttribution: US (nationwide) including the states of AL, AZ, CT, FL, GA, IA, IL, IN, KS, MD, MI, MN, MO, NC, ND, NJ, NM, NV, NY, OH, OR, PA, SC, TX, VA, WA and WY: and Internationally to Canada.
Code information
TITAN Operating Tables: 1465166, 1228073, 1397903, 4544260.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0141-2015
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026