--- title: "Maquet Critical Care AB Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Maquet Critical Care AB recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/maquet-critical-care-ab/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Maquet Critical Care AB recall records **5** reported ongoing 5 records in this archive. Latest source date Jun 30, 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 Jun 30, 2026 FDA device enforcement ### [GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary ...](https://isitonrecall.com/recall/fda-device-z-2963-2026-getinge-y-sensor-module-servo-u-servo-n-model-number-6693662-part-of-the-servo-u-n-continuous-ventil/) The module did not undergo electrical safety tests and functional tests during production. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, GA, MN, NY. [Official source for GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuou...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2963-2026%22) Jun 24, 2026 FDA device enforcement ### [Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900](https://isitonrecall.com/recall/fda-device-z-2860-2026-flow-anesthesia-machine-flow-i-c20-6677200-flow-i-c30-6677300-flow-i-c40-6677400-flow-i-c20-6888520/) Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperative awareness. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution to the states of AL, AR, CA, CO, DC, DE, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, SC, TX, VA, WA, WV. [Official source for Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 68885...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2860-2026%22) May 30, 2025 FDA device enforcement ### [Servo-u Ventilator System. Model Number: 6688600.](https://isitonrecall.com/recall/fda-device-z-2013-2025-servo-u-ventilator-system-model-number-6688600/) Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier. Class I Reported ongoing Distribution: US Nationwide distribution and Puerto Rico. No international distribution. [Official source for Servo-u Ventilator System. Model Number: 6688600.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2013-2025%22) May 30, 2025 FDA device enforcement ### [Servo-n Ventilator System. Model Number: 6694800.](https://isitonrecall.com/recall/fda-device-z-2014-2025-servo-n-ventilator-system-model-number-6694800/) Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier. Class I Reported ongoing Distribution: US Nationwide distribution and Puerto Rico. No international distribution. [Official source for Servo-n Ventilator System. Model Number: 6694800.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2014-2025%22) May 30, 2025 FDA device enforcement ### [Servo-u MR Ventilator System. Model Number: 6888800.](https://isitonrecall.com/recall/fda-device-z-2015-2025-servo-u-mr-ventilator-system-model-number-6888800/) Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier. Class I Reported ongoing Distribution: US Nationwide distribution and Puerto Rico. No international distribution. [Official source for Servo-u MR Ventilator System. Model Number: 6888800.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2015-2025%22) ## Reasons in these listed records - The module did not undergo electrical safety tests and functional tests during production. - Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperative awareness. - Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier. These examples come from this result page and are not a ranking of every recall reason. ## Checking Maquet Critical Care AB ### Is there a recall on maquet critical care ab right now? This archive contains 5 records, including 5 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 Maquet Critical Care AB](https://isitonrecall.com/check/?q=Maquet%20Critical%20Care%20AB) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)