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Trumpf Medical Systems, Inc. recalls TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to
Recalled November 5, 2014 · FDA recall Z-0141-2015 · Trumpf Medical Systems
Hazard
Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes. · FDA Class II
Units
184 units
Sold at
Worldwide Disttribution: US (nationwide) including the states of AL, AZ, CT, FL, GA, IA, IL, IN, KS, MD, MI, MN, MO, NC, ND, NJ, NM, NV, NY, OH, OR, PA, SC, TX, VA, WA and WY: and Internationally to Canada.
Description
Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.
Product
TITAN Operating Room Table 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.
Manufacturer(s)
Trumpf Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →