Data Foundry

Medical device recalls 2016

Stationary Column TruSystem 7599 — Class II medical device recall Z-0041-2017

Terminated recall by Trumpf Medical Systems, Inc., reported 2016-10-12, distributed in CA, CT, GA, IL, NC, OR, SC, VA…. Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Recall numberZ-0041-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTrumpf Medical Systems, Inc., Charleston, SC, United States
Recall initiated2016-07-10
Classified2016-10-05
Reported by FDA2016-10-12
Terminated2017-03-02
DistributedCA, CT, GA, IL, NC, OR, SC, VA, WI, WY
Countries outside the USAU, BR, CH, DE, FI, FR, HU, IT, LU, NO, PL, RU, SK
Quantity84 units
Serial numbers101863421, 101863427, 101863433, 101875827, 101879148, 101879149, 101882031, 101884650, 101884651, 101884653, 101884654, 101890658, 101890659, 101895636, 101904999, 101907202, 101907203

Product

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0041-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.