CLASS II Device recall · Reported 12 Oct 2016 · FDA Enforcement Report

Stationary Column TruSystem recalled by Trumpf Medical Systems

Trumpf Medical Systems is recalling Stationary Column TruSystem 7599, Material Number 1717020 Patient positioning during, distributed in 10 states. The recall was initiated on 10 Jul 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSerial Numbers - 101863421, 101863427, 101863433, 101875827, 101879148, 101879149, 101882031, 101884650, 101884651, 101884653, 101884654, 101890658, 101890659, 101895636, 101904999, 101907202, 101907203
Quantity recalled84 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-0041-2017
FDA event ID
75115
Recalling firm
Trumpf Medical Systems, Charleston, SC
Classification
Class II
Status
Terminated
Recall initiated
10 Jul 2016
FDA classified
5 Oct 2016
Reported
12 Oct 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

10 Jul 2016Recall initiated by company
5 Oct 2016Classified by FDA+87 days
12 Oct 2016Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Product as listed by the FDA

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.

Where it was distributed

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

CaliforniaConnecticutGeorgiaIllinoisNorth CarolinaOregonSouth CarolinaVirginiaWisconsinWyoming

Questions about this recall

Why was it recalled?

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Which lots are affected?

Serial Numbers - 101863421, 101863427, 101863433, 101875827, 101879148, 101879149, 101882031, 101884650, 101884651, 101884653, 101884654, 101890658, 101890659, 101895636, 101904999, 101907202, 101907203

Where was it sold?

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

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 75115

This product is part of a recall event; the main page for the event is Operating Table TruSystem 7000 U, Material Number recalled.

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