Trumpf Medical Systems, Inc. recalls (R)Cable remote control JUPITER, Material no.1219655, Serial number: to (incl.) 101998119. Patient positioning during s…
- Recall date
- December 3, 2014
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0925-2015
- FDA classification
- Class II
- Brand / firm
- Trumpf Medical Systems, Inc.
- Sold / distributed
- Worldwide Distribution - USA including AL, AZ, CA, CT, FL, GA, IL, KS, LA, MD, MI, MK, MS, NC, NH, NJ, NY, OH, OK, PA, RI, SC, TX, VA, WA, WI and Internationally to Canada.
Why it was recalled
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
(R)Cable remote control JUPITER, Material no.1219655, Serial number: to (incl.) 101998119. 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.
Get recall alerts
Free email alert whenever Trumpf Medical Systems, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Trumpf Medical Systems, Inc.