FDA Device recall Z-1736-2022
Verify SixCess Challenge Pack
- FDA Device
- Class III
- terminated
- Published 2022-09-21
On 2022-09-21 the FDA classified a Class III recall of Verify SixCess Challenge Pack by Steris Hopkins Facility, citing product contains incorrect chemical indicators in packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1736-2022 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2022-08-10 |
| Published | 2022-09-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Steris Hopkins Facility |
| Distribution | 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, WY |
Product
Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.
Reason
Product contains incorrect chemical indicators in packaging.
Identifiers
| code_info | UDI-DI (GTIN): 10724995088955 Item Number: LCC003, Lot 3411228A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1736-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.