Hamilton Medical recalls

Hamilton Medical has 34 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 8 Jul 2026. 21 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls34since 2013
Last 12 months2reported
Class I1853% of total
Ongoing21latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 18 53%Class II 15 44%Class III 1 3%

By year

Ongoing hamilton medical recalls

21 active

All hamilton medical recalls, newest first

34 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIIntelliCuff, Portable automatic cuff pressure controller recalledHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IBreathing circuit set, coaxial recalled by Hamilton Medical AGHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IHamilton C6 recalled by Hamilton Medical AGHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IBreathing circuit set, coaxial, 1.80 m, with flow sensor recalledHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IVentilator Hamilton-C6, PN recalled by Hamilton Medical AGHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IHamilton-T1, REF: 161009, Intensive Care and Transport Ventilator recalledHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IHamilton-T1, REF: MSP161339/02, ESM Shielding Set, Spare Part recalledHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IHamilton-C1, REF: 161001, Portable Intensive Care Ventilator recalledHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IHamilton-MR1, REF: 161010, Intensive Care Ventilator recalledHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IHamilton-T1, REF: 161006, Intensive Care and Transport Ventilator recalledHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IHamilton C1/T1/MR1 recalled by Hamilton MedicalHamilton MedicalPackaging DefectsNationwide
DeviceCLASS IHamilton C1 Ventilator recalled by Hamilton MedicalHamilton MedicalDevice Malfunction50 states
DeviceCLASS IHamilton C2 Ventilator Is intended to provide positive recalledHamilton MedicalDevice Malfunction50 states
DeviceCLASS IHamilton T1 Ventilator recalled by Hamilton MedicalHamilton MedicalDevice Malfunction50 states
DeviceCLASS IHamilton C3 Ventilator recalled by Hamilton MedicalHamilton MedicalDevice Malfunction50 states
DeviceCLASS IIHamilton-C6, REF recalled by Hamilton Medical AGHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IIHamilton-C6 recalled by Hamilton Medical AGHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IHamilton-C6 Intensive Care Ventilator recalled by Hamilton Medical AGHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IIIHamilton-H900 Humidifier recalled by Hamilton Medical AGHamilton MedicalDevice Malfunction6 states
DeviceCLASS IHamilton-G5, with software versions less than or equal recalledHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IIHamilton-C1 Ventilator Unit recalled by Hamilton Medical AGHamilton MedicalPotency & Assay9 states
DeviceCLASS IIHamilton-C3 Ventilator Unit recalled by Hamilton Medical AGHamilton MedicalPotency & Assay9 states
DeviceCLASS IIHamilton-C3 Ventilator Unit Intended to provide ventilator recalledHamilton MedicalDevice Malfunction30 states
DeviceCLASS IIHamilton-C2 Ventilator Unit Intended to provide ventilator recalledHamilton MedicalDevice Malfunction30 states
DeviceCLASS IIIntellicuff Standalone (PN 951001) Used to continuously recalledHamilton MedicalOtherIL, TX
DeviceCLASS IIHamilton-MR1 Ventilator recalled by Hamilton MedicalHamilton MedicalOtherNationwide
DeviceCLASS IIHamilton G5 recalled by Hamilton MedicalHamilton MedicalDevice MalfunctionNV
DeviceCLASS IHamilton-G5 Ventilator recalled by Hamilton MedicalHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IIHamilton-G5 Ventilators recalled by Hamilton MedicalHamilton MedicalDevice MalfunctionNationwide
DeviceCLASS IIInfant Flow Sensor, single use, (3.1m) recalled by Hamilton MedicalHamilton MedicalLabeling ErrorsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.