Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stationary Column TruSystem 7599 Recalled by Trumpf Medical Systems, Inc. Due to Three complaints describing TruSystem tables unexpectedly descending approximately...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Trumpf Medical Systems, Inc. directly.
Affected Products
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.
Quantity: 84 units
Why Was This Recalled?
Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.
Where Was This Sold?
This product was distributed to 10 states: CA, CT, GA, IL, NC, OR, SC, VA, WI, WY
About Trumpf Medical Systems, Inc.
Trumpf Medical Systems, Inc. has 30 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report