Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator… — Class II medical device recall Z-0666-2017
Terminated recall by Hamilton Medical, Inc., reported 2016-12-07, distributed nationwide. Oxygen tubing and the oxygen connector of the Hamilton-MR1 could potentially become loose during the preparati
| Recall number | Z-0666-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hamilton Medical, Inc., Reno, NV, United States |
| Recall initiated | 2016-09-26 |
| Classified | 2016-11-28 |
| Reported by FDA | 2016-12-07 |
| Terminated | 2017-03-08 |
| Distributed | Nationwide (US) |
| Quantity | 44 units |
| Model numbers | 161010 |
Product
Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator is intended to provide pressure ventilator support to adults and pediatrics, and optionally infants and neonates. Intended areas of use include: MRI Dept., Intensive, intermediate, emergency and long-term acute care as well as transfer of patients within a hospital.
Reason for recall
Oxygen tubing and the oxygen connector of the Hamilton-MR1 could potentially become loose during the preparation for 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-0666-2017. 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.