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

Recall Z-2057-2015 — Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers for G5: 159001 and 159002. Software: 159700.. Intensive care ventilation of adult and pediatric patients and optionally infant and neonatal patients.

U.S. FDA — Device Enforcement · United States · 2015-03-24 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2057-2015
Date of alert: 2015-03-24
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hamilton Medical, Inc.
Product category: device
Product type: Devices

Reported risk: Customer reports that the ventilator display can freeze. Ventilation continues but the information is no longer displayed on the screen and the user can no longer operate the device.

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

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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-2057-2015 — Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers for G5: 159001 and 159002. Software: 159700.. Intensive care ventilation of adult and pediatric patients and optionally infant and neonatal patients.

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