--- title: "Hamilton Medical AG Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Hamilton Medical AG recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/hamilton-medical-ag/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Hamilton Medical AG recall records **8** reported ongoing 8 records in this archive. Latest source date May 29, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 29, 2026 FDA device enforcement ### [Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.](https://isitonrecall.com/recall/fda-device-z-2463-2026-breathing-circuit-set-coaxial-ref-260127-260128-260167-260168-used-with-hamilton-c1-hamilton-t1-and/) 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 " alarm, which may result in inadequate ventilation, oxygen des... Class I Reported ongoing Distribution: US Nationwide distribution including in the states of KS, WA, VT, TX, WI, AR, OH, PA, CA, CO, ID, AZ, ME, MO, MI, IL, OR, VA, FL, NJ, SD, NY, NM, TN, CT, NE, OK, AL, GA, KY, NH,... [Official source for Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILT...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2463-2026%22) May 22, 2026 FDA device enforcement ### [IntelliCuff, Portable automatic cuff pressure controller REF: 951001](https://isitonrecall.com/recall/fda-device-z-2625-2026-intellicuff-portable-automatic-cuff-pressure-controller-ref-951001/) Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, IL, KY, MA, MI, ND, NE, NE, NY, OH, PA, PR, SD, TX, VA, WA, WI, WV, WY and the country of Canada. [Official source for IntelliCuff, Portable automatic cuff pressure controller REF: 951001](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2625-2026%22) Jun 26, 2025 FDA device enforcement ### [Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.](https://isitonrecall.com/recall/fda-device-z-2167-2025-breathing-circuit-set-coaxial-1-80-m-with-flow-sensor-and-expiratory-valve-set-ref-260128-used-with/) Ventilator coaxial breathing circuit may have a crack in blue tubing, which is used to deliver fresh gas to the patient. The crack will compromise inspiratory and expiratory flows, leading to partial or complete rebreathing of exhaled gases, which could lea... Class I Reported ongoing Distribution: US Nationwide distribution in the states of NH, NY, CT, PA, IL, ME, CO, NC, NJ, UT, TX, GA, SC, VA, IN, SD, MO, OR, TN, MA, AZ, NM. [Official source for Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, u...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2167-2025%22) Jun 3, 2025 FDA device enforcement ### [Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ventilator intended to provide positive pressure ventilatory support to adults and...](https://isitonrecall.com/recall/fda-device-z-2328-2025-hamilton-c6-ref-160021-esm-board-pn-10144626-udi-di-code-76300028pn160021zw-hamilton-c6-is-a-ventila/) A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interr... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ve...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2328-2025%22) May 15, 2024 FDA device enforcement ### [Ventilator HAMILTON-C6, PN: 160021](https://isitonrecall.com/recall/fda-device-z-2020-2024-ventilator-hamilton-c6-pn-160021/) Ventilator may enter sensor fail mode, ventilation may not re-initiate, after patient is reconnected, which may cause hypoxia, if this sequence occurs: 1)User presses O2 enrichment, 2)User disconnects endotracheal tube for open suctioning, 3)Sensor error in... Class I Reported ongoing Distribution: US Nationwide distribution in the states of GA, KY, FL, IN, NV, MI, VA, OR, TX, SC, CA, PA. [Official source for Ventilator HAMILTON-C6, PN: 160021](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2020-2024%22) Mar 14, 2023 FDA device enforcement ### [HAMILTON-C6, REF: 160021](https://isitonrecall.com/recall/fda-device-z-1429-2023-hamilton-c6-ref-160021/) Software error causes, safety ventilation, in which ventilation continues in the "safety ventilation" mode with audible/visible alarm - patient inputs are not monitored, if the following coincide 1) A mode change to an adaptive mode (ASV, APVcmv, APVsimv, I... Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, MA, ID, NC, GA, FL, NV, PA, MO, KS, SC, NY, NM, WY, VA. [Official source for HAMILTON-C6, REF: 160021](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1429-2023%22) Sep 22, 2022 FDA device enforcement ### [Hamilton-C6](https://isitonrecall.com/recall/fda-device-z-0267-2023-hamilton-c6/) Due to a malfunction related to the backlight on the ventilator screen. The screen goes black for approximately 2-3 seconds, but it brightens up again when the backlight switches on again. Class II Reported ongoing Distribution: U.S. Nationwide distribution including in the states of CA, FL, GA, ID, IN, KS, KY, MA, MI, MO, NV, NM, NY, NC, OH, PA, Puerto Rico, SC, TX, VA, WA, WV, WI, and WY. [Official source for Hamilton-C6](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0267-2023%22) Jun 27, 2022 FDA device enforcement ### [HAMILTON-C6 Intensive Care Ventilator, REF: 160021](https://isitonrecall.com/recall/fda-device-z-1525-2022-hamilton-c6-intensive-care-ventilator-ref-160021/) Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety Ventilation (blower runs constantly) o... Class I Reported ongoing Distribution: US nationwide distribution including Puerto Rico. [Official source for HAMILTON-C6 Intensive Care Ventilator, REF: 160021](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1525-2022%22) ## Reasons in these listed records - 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 " alarm, which may result in inadequate ventilation, oxygen desaturation. Advising:... - Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user. - Ventilator coaxial breathing circuit may have a crack in blue tubing, which is used to deliver fresh gas to the patient. The crack will compromise inspiratory and expiratory flows, leading to partial or complete rebreathing of exhaled gases, which could lead to acute hypercapn... - A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interruption of ventilation. These examples come from this result page and are not a ranking of every recall reason. ## Checking Hamilton Medical AG ### Is there a recall on hamilton medical ag right now? This archive contains 8 records, including 8 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Hamilton Medical AG](https://isitonrecall.com/check/?q=Hamilton%20Medical%20AG) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)