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

Recall Z-0170-2014 — HAMILTON-C2 Ventilator: Manufactured by Hamilton Medical AG CH-7402 Bonaduz, Switzerland; Imported and distributed by Hamilton Medical, Inc. Reno, NV 89502 The HAMILTON C2 ventilator is intended to provide positive pressure ventilatory support to adults, pediatrics, infants and neonates depe

U.S. FDA — Device Enforcement · United States · 2013-09-26 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0170-2014
Date of alert: 2013-09-26
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hamilton Medical, Inc.
Product category: device
Product type: Devices

Reported risk: Manufacturer defined limits for improperly functioning loudspeakers of the HAMILTON C2 alarm system were exceeded.

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.

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