Steris Corporation recalls V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)

Recalled March 7, 2018 · FDA recall Z-0772-2018 · Steris

Hazard

Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle. · FDA Class II

Units

406

Sold at

Distributed in 44 states: AL, AK, AZ, AR, CA, CO, DE, FL, GA, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY; Puerto Rico, and the following countries: Algeria, Australia, Azerbaijan, Bahrain, Brazil, Brunei Darussalam, Bulgaria, Canada, Chile, Colombia, Costa Rica, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Hong Kong, Hungary, India, Israel, Italy, Republic of Korea, Kuwait, Latvia, Malaysia, Mexico, Morocco, Myanmar, Panama, Peru, Philippines, Poland, Portugal, Qatar, Saudi Arabia, South Africa, Spain, Switzerland, Thailand, Turkey, United Arab Emirates, and Vietnam.

Description

Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.

Product

V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)

Manufacturer(s)

Steris Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →