Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(R)IR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to Complaints have been reported of unintended movement occurring...
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
(R)IR remote control JUPITER, Material no.1219656, Serial number: to (incl.) 102317869. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
Quantity: 3303 total all devices
Why Was This Recalled?
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
Where Was This Sold?
This product was distributed to 25 states: AL, AZ, CA, CT, FL, GA, IL, KS, LA, MD, MI, MS, NH, NJ, NY, NC, OH, OK, PA, RI, SC, TX, VA, WA, WI
About Trumpf Medical Systems, Inc.
Trumpf Medical Systems, Inc. has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report