Hamilton Medical AG recalls
Every recall we track for Hamilton Medical AG — 14 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Hamilton Medical AG peaked in 2018 (4); 14 since 2017.
All FDA recall records for Hamilton Medical AG since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 3 | 1 | 0 | 4 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 1 | 1 | 0 | 2 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 2 | 0 | 0 | 2 |
| 2026 (to date) | 0 | 2 | 0 | 0 | 2 |
What to do if you have a recalled Hamilton Medical AG product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Hamilton Medical AG recalls
12 shown- Use cautionMedical device
Hamilton Medical AG recalls Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1
Hamilton Medical recalls coaxial breathing circuit sets (REFs 260127-260168) used with C1/T1/MR1 ventilators. Membranes may stick to valves, causing exhalation obstruction and oxygen desaturation if not tested before use.
Hamilton MedicalMay 29, 2026 - Use cautionMedical device
Hamilton Medical AG recalls IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Hamilton Medical recalls IntelliCuff portable blood pressure cuffs with REF 951001 due to potential "Cuff System Leakage" error causing continuous motor operation and pressure failure.
Hamilton MedicalMay 22, 2026 - Use cautionMedical device
Hamilton Medical AG recalls Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1,
Hamilton Medical recalls breathing circuits with possible blue tubing cracks that could cause rebreathing of exhaled gases, leading to respiratory issues. Affected units include specific model numbers and serial lots.
Hamilton MedicalJun 26, 2025 - Use cautionMedical device
Hamilton Medical AG recalls Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ventilator intended to
Hamilton Medical recalls C6 ventilators with specific serial numbers due to a PCB defect that can cause ventilation failure. Affected units may stop working during use, risking interrupted breathing support.
Hamilton MedicalJun 3, 2025 - Use cautionMedical device
Hamilton Medical AG recalls Ventilator HAMILTON-C6, PN: 160021
Hamilton Medical recalls HAMILTON-C6 ventilators with specific software versions due to potential hypoxia if sensor fail mode occurs after patient reconnection. Affected units have UDI 07630002808590 and software versions v1.1.4 to v1.1.6.
Hamilton MedicalMay 15, 2024 - Use cautionMedical device
Hamilton Medical AG recalls HAMILTON-C6, REF: 160021
Hamilton Medical recalls C6 ventilators with software version 1.2.1 due to safety ventilation mode not monitoring patient inputs, risking undetected issues during certain settings.
Hamilton MedicalMar 14, 2023 - Lower riskMedical device
Hamilton Medical AG recalls Hamilton-C6
Hamilton Medical recalls C6 ventilators with serial numbers starting 6093-9590 due to temporary screen blackouts. This may affect patient monitoring but does not cause injury.
Hamilton MedicalSep 22, 2022 - Use cautionMedical device
Hamilton Medical AG recalls HAMILTON-C6 Intensive Care Ventilator, REF: 160021
Hamilton Medical recalls C6 ventilators with serial numbers starting 5663-9590 due to loose status indicator board risking water ingress from disinfectants, potentially causing technical faults and unsafe breathing conditions.
Hamilton MedicalJun 27, 2022 - Use cautionMedical device
Hamilton Medical AG recalls HAMILTON-H900 Humidifier, Models: 950001, 950004
Hamilton Medical recalls H900 humidifiers (models 950001, 950004) with software 1.10c due to delayed low water alarm when chamber is empty, risking undetected water absence during medical ventilation.
Hamilton MedicalJan 5, 2021 - Use cautionMedical device
Hamilton Medical AG recalls HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for
Hamilton Medical recalls G5 ventilators with software versions 2.60 or older due to potential risk of unassisted breathing. Affected units have serial numbers 16192 and lower.
Hamilton MedicalMar 25, 2019 - Use cautionMedical device
Hamilton Medical AG recalls Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and
Hamilton Medical recalls C2 Ventilators due to battery gauge potentially showing higher charge than actual. This could lead to unexpected shutdowns during critical care. Affected units have serial numbers and were sold in hospitals.
Hamilton MedicalMar 12, 2018 - Use cautionMedical device
Hamilton Medical AG recalls Hamilton-C3 Ventilator Unit Product Usage: The HAMILTON-C3 ventilator is intended to provide positive pressure
Hamilton Medical recalls C3 ventilators with potential for unintended shutdown due to control board issues. Affected units may shut down unexpectedly with alarms. Contact for remedy details.
Hamilton MedicalMar 9, 2018
Hamilton Medical AG recall questions
How many recalls has Hamilton Medical AG had?
14 recalls from Hamilton Medical AG are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Hamilton Medical AG recall?
Hamilton Medical AG recalls Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1, dated May 29, 2026. Every Hamilton Medical AG recall is listed on this page, newest first.
What should I do if I have a recalled Hamilton Medical AG product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Hamilton Medical AG recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.