Drug recall
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and…
FDA recall event 99028 · Class I · Hamilton Medical AG
Key facts
| Event ID | 99028 |
|---|---|
| Recall numbers | Z-2463-2026 |
| Recalling firm | Hamilton Medical AG |
| Product type | Devices |
| Products | Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators. |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result in "exhalation obstructed "… |
| Initiation date | May 29, 2026 |
| Report date | Jul 8, 2026 |
| City | Domat/Ems |
| Country | Switzerland |
| FEI number | 3014766741 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: