Data Foundry

Medical device recalls 2023

Hamilton-C1 — Class I medical device recall Z-2525-2023

Ongoing recall by Hamilton Medical, Inc., reported 2023-09-27, distributed nationwide. Degrading capacitors on the control board of ventilators and spare parts may leak electrolyte onto the control

Recall numberZ-2525-2023
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmHamilton Medical, Inc., Reno, NV, United States
Recall initiated2023-07-26
Classified2023-09-20
Reported by FDA2023-09-27
DistributedNationwide (US)
Quantity164 units
Reason classespackaging, device malfunction
UPC / GTIN / UDI-DI07630002800747, 07630002813426
Serial numbers24177, 24196, 24216, 24217, 24219, 24247, 24250, 24324, 24360, 24370, 24431, 24460, 24467, 24480, 24487, 24511, 24523, 24552, 24556, 24557, 24558, 24561, 24564, 24565, 24571 and 139 more
Model numbers161001

Product

Hamilton-C1, REF: 161001, Portable Intensive Care Ventilator

Reason for recall

Degrading 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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2525-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.