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

Recall Z-1793-2022 — a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack Steam 3 Inch Length Model Number: LCB053. b. STERIS CORP VERIFY Verify SixCess Sterilization Flash Indicator Strip Steam 2-3/4 Inch Model Number: PCC006. c. STERIS CORP VERIFY Verify Sterilization Biological Indicator Pac

U.S. FDA — Device Enforcement · United States · 2022-05-25 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1793-2022
Date of alert: 2022-05-25
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Mckesson Medical-Surgical Inc. Corporate Office
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00724995161569

Reported risk: Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

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.

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