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
StatusOngoing
ReasonDegrading capacitors on the control board of ventilators and spare parts may leak electrolyte onto the control board causing a short circuit on the board and/or the capacitor to lose function and lead to interruption of ventilation.
ProductHamilton-T1, REF: 161009, Intensive Care and Transport Ventilator
Quantity1216 units
DistributionDistribution US nationwide, including Puerto Rico. OUS: Not provided
Initiated2023-07-26
Classified2023-09-20
Recall numberZ-2527-2023
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-2527-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92873/

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