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Med Tec Inc recalls Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioni
Recalled June 10, 2020 · FDA recall Z-2243-2020 · Med Tec
Hazard
Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff. · FDA Class II
Units
171 units
Sold at
Worldwide distribution - US Nationwide distribution including in the states of WI, TX, AZ, FL, NE, TN, MA, FL, GA, IN, OR, PA, IL, LA, NH, MS, MI, OH, MN, VA, IA, CA, NC, SC, AK, UT, WA, MO, MT, KS, and WV. The countries of Africa, Colombia, Saudi Arabia, Costa Rica, South Korea, Hungary, Spain, and Italy.
Description
Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff.
Product
Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning.
Manufacturer(s)
Med Tec Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →