--- title: "Draeger Medical, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Draeger Medical, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/draeger-medical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Draeger Medical, Inc. recall records **10** reported ongoing 35 records in this archive. Latest source date Oct 15, 2024. 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 Oct 15, 2024 FDA device enforcement ### [Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicable](https://isitonrecall.com/recall/fda-device-z-0304-2025-brand-name-atlan-product-name-atlan-a350-model-catalog-number-8211500-software-version-not-applicabl/) The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. Class I Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, FL, GA, IA, IL, KY, MA, ME, ND, NE, NH, NJ, NY, OH, PA, TN, TX, WI, WY. International distribution: Argentina, Australia,... [Official source for Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not ap...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0304-2025%22) Oct 15, 2024 FDA device enforcement ### [Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable](https://isitonrecall.com/recall/fda-device-z-0305-2025-brand-name-atlan-product-name-atlan-a350xl-model-catalog-number-8621600-software-version-not-applica/) The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. Class I Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, FL, GA, IA, IL, KY, MA, ME, ND, NE, NH, NJ, NY, OH, PA, TN, TX, WI, WY. International distribution: Argentina, Australia,... [Official source for Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0305-2025%22) Oct 15, 2024 FDA device enforcement ### [Brand Name: Atlan Product Name: Atlan A300 Model/Catalog Number: 8211300 The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates.](https://isitonrecall.com/recall/fda-device-z-0667-2025-brand-name-atlan-product-name-atlan-a300-model-catalog-number-8211300-the-atlan-is-an-anesthesia-wor/) The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. Class I Reported ongoing Distribution: No Atlan A300 or A300XL devices were imported into the US. Devices were direct shipped from Draegerwerk Ag and Co. KGaA to the following countries: Argentina, Australia, Austria... [Official source for Brand Name: Atlan Product Name: Atlan A300 Model/Catalog Number: 8211300 The Atlan is an anesthes...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0667-2025%22) Oct 15, 2024 FDA device enforcement ### [Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neona...](https://isitonrecall.com/recall/fda-device-z-0668-2025-brand-name-atlan-product-name-atlan-a300xl-model-catalog-number-8621400-the-atlan-is-an-anesthesia-w/) The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. Class I Reported ongoing Distribution: No Atlan A300 or A300XL devices were imported into the US. Devices were direct shipped from Draegerwerk Ag and Co. KGaA to the following countries: Argentina, Australia, Austria... [Official source for Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesth...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0668-2025%22) Mar 20, 2024 FDA device enforcement ### [Dr¿ger Perseus A500 Anesthesia Workstation](https://isitonrecall.com/recall/fda-device-z-1512-2024-dr-ger-perseus-a500-anesthesia-workstation/) Unexpected shutdown while operating on battery power. Class I Reported ongoing Distribution: Domestic: Nationwide Distribution; Foreign: Angola, Argentina, Australia, Austria, Bahrain, Belarus, Belgium, Bolivia, Botswana, Brazil, Brunei Dar-se- S, Bulgaria, Canada, Chil... [Official source for Dr¿ger Perseus A500 Anesthesia Workstation](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1512-2024%22) Jul 12, 2023 FDA device enforcement ### [Carina Sub-Acute Care Ventilator](https://isitonrecall.com/recall/fda-device-z-2248-2023-carina-sub-acute-care-ventilator/) Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients. Class I Reported ongoing Distribution: US Nationwide Distribution. [Official source for Carina Sub-Acute Care Ventilator](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2248-2023%22) Jun 12, 2023 FDA device enforcement ### [Oxylog 3000 Plus emergency and transport ventilator](https://isitonrecall.com/recall/fda-device-z-2018-2023-oxylog-3000-plus-emergency-and-transport-ventilator/) Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation. Class I Reported ongoing Distribution: Distributed Nationwide. OUS Distribution: Afghanistan, Algeria, Andorra, Angola, Antigua/Barbados, Argentina, Australia, Austria, Azerbaijan, Bahrain, Belarus, Belgium, Bolivia,... [Official source for Oxylog 3000 Plus emergency and transport ventilator](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2018-2023%22) Apr 17, 2023 FDA device enforcement ### [Seattle PAP Plus, MP02260](https://isitonrecall.com/recall/fda-device-z-1439-2023-seattle-pap-plus-mp02260/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for Seattle PAP Plus, MP02260](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1439-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Basic (P)180, MP00351](https://isitonrecall.com/recall/fda-device-z-1440-2023-ventstar-basic-p-180-mp00351/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Basic (P)180, MP00351](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1440-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Basic (P)250, MP00352](https://isitonrecall.com/recall/fda-device-z-1441-2023-ventstar-basic-p-250-mp00352/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Basic (P)250, MP00352](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1441-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Watertrap (P) 180, MP00361](https://isitonrecall.com/recall/fda-device-z-1442-2023-ventstar-watertrap-p-180-mp00361/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Watertrap (P) 180, MP00361](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1442-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Watertrap (P) 180 w/oLL, MP00362](https://isitonrecall.com/recall/fda-device-z-1443-2023-ventstar-watertrap-p-180-w-oll-mp00362/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Watertrap (P) 180 w/oLL, MP00362](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1443-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Anesthesia WT (P)180, MP00374](https://isitonrecall.com/recall/fda-device-z-1444-2023-ventstar-anesthesia-wt-p-180-mp00374/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Anesthesia WT (P)180, MP00374](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1444-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar breathing bag Set (P) 110, MP00384](https://isitonrecall.com/recall/fda-device-z-1445-2023-ventstar-breathing-bag-set-p-110-mp00384/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar breathing bag Set (P) 110, MP00384](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1445-2023%22) Apr 17, 2023 FDA device enforcement ### [ID Circuit Basic (P) 180, MP01340](https://isitonrecall.com/recall/fda-device-z-1446-2023-id-circuit-basic-p-180-mp01340/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for ID Circuit Basic (P) 180, MP01340](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1446-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Anesthesia (N) 180, MP00333](https://isitonrecall.com/recall/fda-device-z-1447-2023-ventstar-anesthesia-n-180-mp00333/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Anesthesia (N) 180, MP00333](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1447-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Basic (N) 180, MP00353](https://isitonrecall.com/recall/fda-device-z-1448-2023-ventstar-basic-n-180-mp00353/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Basic (N) 180, MP00353](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1448-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Watertrap (N) 180, MP00363](https://isitonrecall.com/recall/fda-device-z-1449-2023-ventstar-watertrap-n-180-mp00363/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Watertrap (N) 180, MP00363](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1449-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Bag Set (N) 110, MP00383](https://isitonrecall.com/recall/fda-device-z-1450-2023-ventstar-bag-set-n-110-mp00383/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Bag Set (N) 110, MP00383](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1450-2023%22) Apr 17, 2023 FDA device enforcement ### [VentStar Coax (P) 150, MP00379](https://isitonrecall.com/recall/fda-device-z-1451-2023-ventstar-coax-p-150-mp00379/) Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. Class I Reported terminated Distribution: Domestic: US Nationwide Distribution. [Official source for VentStar Coax (P) 150, MP00379](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1451-2023%22) ## Reasons in these listed records - The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. - Unexpected shutdown while operating on battery power. - Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients. - Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation. These examples come from this result page and are not a ranking of every recall reason. ## Checking Draeger Medical, Inc. ### Is there a recall on draeger medical, inc. right now? This archive contains 35 records, including 10 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 Draeger Medical, Inc.](https://isitonrecall.com/check/?q=Draeger%20Medical%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)