Trumpf Medical Systems Recalls Stationary Column TruSystem 7599 Operating Tables
Trumpf Medical Systems is recalling 84 Stationary Column TruSystem 7599 units because they may unexpectedly descend approximately 20 centimeters.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device defect that poses a risk of harm (unexpected descent) but the source text does not report any injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Trumpf Medical Systems, Inc. is recalling 84 units of the Stationary Column TruSystem 7599, Material Number 1717020. These medical devices are used for patient positioning during surgery, ranging from anesthesia induction to recovery, and for patient transport on the operating table top.
The recall was initiated due to three complaints describing the TruSystem tables unexpectedly descending approximately 20 centimeters. This defect poses a risk of patient injury if the table height changes unexpectedly during use.
The affected units were distributed worldwide, including in the United States (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. Specific serial numbers are listed in the official recall notice. Healthcare facilities should contact Trumpf Medical Systems for instructions on how to address the defect.
The recalled product
- 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…
- Manufacturer
- Trumpf Medical Systems, Inc.
- Category
- Medical Device — Operating Table
- Affected units
- 84
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (17)
- Serial Numbers - 101863421
- 101863427
- 101863433
- 101875827
- 101879148
- 101879149
- 101882031
- 101884650
- 101884651
- 101884653
- 101884654
- 101890658
- 101890659
- 101895636
- 101904999
- 101907202
- 101907203
Distribution
Part of a larger recall action
This product is one of 4 recalled by Trumpf Medical Systems, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
Same manufacturer · Trumpf Medical Systems, Inc.
See all →- ModerateTrumpf Medical Systems Recalls Surgical Camera Systems Due to Emission Issues
FDA (Devices) · 2018-03-07
- HighTrumpf Medical Systems Recalls Operating Room Table Tops for Cable Pinching
FDA (Devices) · 2016-11-16
- HighTrumpf Medical Systems Recalls Floor Mounting Columns for Unexpected Descent
FDA (Devices) · 2016-10-12
- SevereTrumpf Medical Systems Recalls TruSystem Mobile Operating Columns
FDA (Devices) · 2016-10-12
- HighTrumpf Medical Systems Recalls TruSystem Operating Tables Due to Unexpected Descent
FDA (Devices) · 2016-10-12
Same hazard · unexpected descent
See all →- HighPhilips CT Systems Patient Support Table May Descend Unexpectedly
FDA (Devices) · 2025-10-01
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