Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Verify SixCess Challenge Pack. Used to confirm that critical parameters Recalled by Steris Corporation Hopkins Facility Due to Product contains incorrect chemical indicators in packaging.

Date: August 10, 2022
Company: Steris Corporation Hopkins Facility
Status: Terminated
Source: FDA (Device)

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 Hopkins Facility directly.

Affected Products

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

Quantity: 619 boxes

Why Was This Recalled?

Product contains incorrect chemical indicators in packaging.

Where Was This Sold?

This product was distributed to 31 states: AK, AZ, AR, CA, CO, FL, GA, ID, IL, IN, IA, KY, LA, MA, MN, MS, MO, NE, NH, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WY

Affected (31 states)Not affected

About Steris Corporation Hopkins Facility

Steris Corporation Hopkins Facility has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report