Medical device recalls

Steris Corporation Hopkins Facility recalls Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…

Recall date
August 10, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1736-2022
FDA classification
Class III
Brand / firm
Steris Corporation Hopkins Facility
Sold / distributed
Distribution in the US only - AK, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MN, MO, MS, NE, NH, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, and WY

Why it was recalled

Product contains incorrect chemical indicators in packaging.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.

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