Hamilton Medical AG recalls Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamil…

A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interruption of ventilation.

URGENT: Medical Device Correction letters were emailed to customers on 06/06/2025, 06/20/2025, and 07/07/2025, informing them that due to damage to the capacitor in the ESM-Board within the Hamilton-C6 ventilator the capacitor could, over time, lead to a loss of its function due to oxidation of similar degradation processes. Customers are instructed to: 1. Review their Hamilton-C6 ventilators and check for the serial number within the scope mentioned in the letter. 2. for affected ventilators must have the ESM-Boards replaced. The replacement will be organized by the local partner as per servicing protocol. Note - the Hamilton-C6 ventilators do not need to be removed from use/service. These devices were tested prior to release and no test will be able to detect if the ESM board will fail in the future. 3. Keep the recall notice within the respective ventilator's data records. For questions or assistance, contact Technical Support at 1-800-426-6331 option 2 or email reno.techsupport@hamiltonmedical.com

• FDA enforcement recordOfficial FDA database entry for Z-2328-2025
• FDA 510(k) clearance · K201658The device's official FDA premarket clearance record
• FDA device classification · CBKOfficial FDA classification for this device type
• CFR regulation · 21 CFR 868.5895The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Hamilton Medical AGSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.