RegWardenFDA facility compliance records
Recall

Class I — Hamilton Medical Inc

Recalling firmHAMILTON MEDICAL, INC.
Registered facilityHAMILTON MEDICAL, INC. (the firm's only registered facility)
ClassificationClass I
StatusTerminated
ReasonAnalysis of a customer complaint has shown that during ventilation of small pediatric patients with high airway resistance and low lung compliance, the oxygen consumption of a Hamilton T1 ventilator with software versions 1.1.2 and lower must be calculated using a larger margin than originally expected.
ProductHAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON T-1 Ventilator is intended to provide positive pressure ventilatory support to adults and pediatrics
Quantity97 total ventilators; 69 of part number 161005 and 28 of part number 161006
DistributionUS Nationwide Distribution including the country of Switzerland.
Initiated2012-12-19
Classified2013-01-31
Terminated2014-04-22
Recall numberZ-0741-2013
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class I recall — Hamilton Medical Inc (Z-0741-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/64117/

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