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

Recall Z-1779-2019 — Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and materials used in the health

U.S. FDA — Device Enforcement · United States · 2019-04-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1779-2019
Date of alert: 2019-04-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Skytron, Div. The KMW Group, Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 14092619

Reported risk: Weld attaching the air heater assembly to the main sterilizer unit has shown signs of fatigue/failure

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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