Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) Recalled by Steris Corporation Due to Correction to update sterilizer software to prohibit the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Steris Corporation directly.
Affected Products
V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)
Quantity: 406
Why Was This Recalled?
Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.
Where Was This Sold?
This product was distributed to 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
About Steris Corporation
Steris Corporation has 109 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report