Reported Jan 14, 2015 · Terminated

IR remote control JUPITER U, Material no. 4500120, Serial number: to (incl.) 102306940. Patient positioning during…

Trumpf Medical Systems, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Trumpf Medical Systems, Inc. · 1046 Legrand Blvd · Charleston, SC · 29492-7672

Is this the product you have?

  • IR remote control JUPITER U, Material no. 4500120
  • Serial numberto (incl.) 102306940. 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
Lot codes and dates

9 of 9 products

Products covered by this recall
#Product as published
1Mobile column JUPITER System U, Material no. 4500113
2Mobile column JUPITER System Miyabi U, Material no. 1574977
3Operating table column JUPITER SM 360 U, Material no. 1389824
4Operating table column JUPITER SF U OCE, Material no. 1622774
5Stationary column JUPITER System U, Material no. 4500112
6FLOOR MOUNTING COLUMN JUPITER U, Material no. 1276277
7Floor mounting column JUPITER 360 U, Material no.1389826
8Operating table JUPITER UNIVERSAL U, Material no. 4500170
9OR-TABLE JUPITER UNIVERSAL CARBON U, Material no.1223188.
Amount recalled
3303 total all devices

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 23, 2016 · Data as of Sep 19, 4:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.