Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1736-2022 — Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.

U.S. FDA — Device Enforcement · United States · 2022-08-10 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1736-2022
Date of alert: 2022-08-10
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Steris Corporation Hopkins Facility
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10724995088955

Reported risk: Product contains incorrect chemical indicators in packaging.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1736-2022 — 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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