Steris Corporation Hopkins Facility: Medical Device Recall in 2022 - (Recall #: Z-1736-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class III

Date Initiated: August 10, 2022

Date Posted: September 21, 2022

Recall Number: Z-1736-2022

Event ID: 90763

Reason for Recall:

Product contains incorrect chemical indicators in packaging.

Status: Terminated

Product Quantity: 619 boxes

Code Information:

UDI-DI (GTIN): 10724995088955 Item Number: LCC003, Lot 3411228A

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated