Z-0041-2017 Class II Terminated
FDA device recall Z-0041-2017 was initiated by Trumpf Medical Systems, Inc. on Jul 10, 2016 and is designated Class II. Reason for recall: Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters. The recall status is terminated (terminated Mar 2, 2017). Affected quantity: 84 units.
Recall details
- Product Type
- Devices
- Report Date
- Oct 12, 2016
- Initiation Date
- Jul 10, 2016
- Termination Date
- Mar 2, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 84 units
Product description
Stationary Column TruSystem 7599, Material Number 1717020 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient transfer system to the operating theater of from the operating theater to a patient transfer system.
Reason for recall
Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.
Distribution pattern
Worldwide Distribution - US including CA, CT, GA, IL, NC, OR, SC, VA, WI, WY, and Internationally to Australia, Azerbaijan, Brazil, Finland, France, Germany, Hungary, Italy, Luxembourg, Norway, Poland, Russia, Slovakia, and Switzerland
Code information
Serial Numbers - 101863421, 101863427, 101863433, 101875827, 101879148, 101879149, 101882031, 101884650, 101884651, 101884653, 101884654, 101890658, 101890659, 101895636, 101904999, 101907202, 101907203
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0041-2017
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026