RecallRadar

FDA Device recall Z-0929-2015

IR remote control JUC, BUTTON, Material no.1239824, Serial number: to (incl.) 100139854

On 2015-01-14 the FDA classified a Class II recall of IR remote control JUC, BUTTON, Material no.1239824, Serial number: to (incl.) 100139854 by Trumpf Medical Systems, citing complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0929-2015
ClassificationClass II
Statusterminated
Initiated2014-12-03
Published2015-01-14
Last updated2026-09-13 11:53 UTC
CompanyTrumpf Medical Systems
DistributionAL, AZ, CA, CT, FL, GA, IL, KS, LA, MD, MI, MS, NC, NH, NJ, NY, OH, OK, PA, RI, SC, TX, VA, WA, WI

Product

IR remote control JUC, BUTTON, Material no.1239824, Serial number: to (incl.) 100139854. 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.

Reason

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Identifiers

code_info
The operating tables which are operated with the affected remote controls (all serial numbers): Mobile column JUPITER S…The operating tables which are operated with the affected remote controls (all serial numbers): Mobile column JUPITER System U, Material no. 4500113; Mobile column JUPITER System Miyabi U, Material no. 1574977; Operating table column JUPITER SM 360 U, Material no. 1389824; Operating table column JUPITER SF U OCE, Material no. 1622774; Stationary column JUPITER System U, Material no. 4500112; FLOOR MOUNTING COLUMN JUPITER U, Material no. 1276277; Floor mounting column JUPITER 360 U, Material no.1389826; Operating table JUPITER UNIVERSAL U, Material no. 4500170; OR-TABLE JUPITER UNIVERSAL CARBON U, Material no.1223188.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0929-2015%22

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