Every recall we track for Draeger Medical, Inc. — 64 in all — plus the complaints and injury reports the public filed about them.
Draeger recalls Atlan A300 anesthesia workstations with model 8211300 due to potential piston ventilator failure before use or mechanical ventilation failure during use. Affected units have specific serial numbers.
Draeger Medical recalls Atlan A350 anesthesia workstations with model 8211500 due to risk of piston ventilator failure before or during use. Affected units have specific serial numbers listed in the recall.
Draeger recalls Atlan A350XL anesthesia workstations with model 8621600 due to risk of piston ventilator failure before or during use. Affected units have specific serial numbers listed in the recall.
Draeger recalls Atlan A300XL anesthesia workstations (model 8621400) due to potential piston ventilator failure before use or mechanical ventilation failure during use. Affected units have specific serial numbers.
Draeger Medical recalls Perseus A500 anesthesia workstations that may unexpectedly shut down on battery power, risking patient safety during surgery.
Draeger Medical recalls pediatric ventilators due to chemical emissions exceeding safe levels during long-term use. Affected units may pose health risks for children.
Draeger recalls Oxylog 3000 Plus ventilators that may stop working when switching from battery to AC power. Affected units have specific catalog numbers and serials. Contact for repair or replacement.
Draeger Medical recalls Ventstar Coax 230 devices due to risk of breathing circuit detachment during ventilation. All units are affected.
Draeger Medical recalls VentStar Basic 180 ventilators due to risk of breathing circuit pieces detaching during ventilation. All units are affected.
Draeger Medical recalls Anesthesia Circuit Kit Coax 1 (MP02730) due to glued connections that can become loose, potentially causing partial or complete detachment during ventilation. All units are affected.
Draeger Medical recalls Ventstar Coax 180 devices due to risk of breathing circuit detachment during ventilation. All units are affected.
Draeger Medical recalls Anesthesia Circuit Kit Coax 3 (MP02732) due to glued connections that may become loose, causing partial or complete detachment during ventilation. All units are affected.
Draeger Medical recalls VentStar Basic (P)250 ventilators due to risk of breathing circuit detachment from loose connections during ventilation. All units are affected.
Draeger Medical recalls ID Circuit Basic (P) 18:00 models with loose breathing circuit connections that may detach during ventilation, causing breathing issues. Affected units include all lots sold.
Draeger Medical recalls Ventstar Coax MP033: Glued connections may become loose during ventilation, causing partial or complete detachment of breathing circuit pieces. All units affected.
Draeger Medical recalls VentStar Anesthesia 180 models due to risk of breathing circuit detachment during use. Affected units have specific serial numbers and were sold in the U.S. Learn how to check and what to do.
Draeger Medical recalls VentStar Watertrap 180 models due to risk of breathing circuit parts detaching during ventilation. Affected units have specific serial numbers and were sold from 2013 onward.
Draeger Medical recalls VentStar Watertrap 180 models due to risk of breathing circuit detachment during ventilation. Affected units have specific UDI-DI numbers and all lots.
Draeger Medical recalls Anesthesia Set Coax 180 (MP03384) due to potential loose breathing circuit connections that could detach during use. All units are affected.
Draeger Medical recalls VentStar Anesthesia WT (P)180 models due to risk of breathing circuit detachment during use. Affected units may require repair or replacement to prevent injury.
Draeger Medical recalls Seattle PAP Plus devices with model MP02260 sold before March 20, 2023. Glued breathing circuit connections can become loose, causing partial or complete detachment of pieces during ventilation.
Draeger Medical recalls Set2Go Ventilation 12 (A) units due to risk of breathing circuit parts detaching during ventilation. All units are affected. Contact for remedy.
Draeger Medical recalls VentStar Basic (P)180 ventilators due to risk of breathing circuit pieces detaching during use, potentially causing breathing issues.
Draeger Medical recalls NovaStar TS anti-asphyxia valve reusable sets with magnet risk for medical devices and implants. Affected models include sizes S, M, L with specific material numbers and lot numbers.
Draeger Medical recalls NovaStar TS elbow sets with magnets that could interfere with medical implants and devices. Affected units have specific material numbers and lot numbers.
Draeger Medical recalls SafeStar 55 oxygen monitors with possible filter blockage due to manufacturing error. Affected units have specific catalog and lot numbers. No remedy stated in recall notice.
Draeger Medical recalls Babylog VN500 ventilators with software 2.51.01 due to cybersecurity vulnerabilities affecting neonatal and pediatric patients.
Draeger Medical recalls Evita V500 ventilators with software 2.51.01 and lower due to cybersecurity vulnerabilities. All units are affected; no specific remedy is provided in the recall notice.
Draeger recalls 26 Fabius MRI Anesthesia Machines with oxygen flow control error that may cause patient oxygenation issues if central oxygen pressure is unstable.
Draeger Medical recalls Evita V500 ventilators with CO2 measurement software 2.51 or lower. This version may cause brief pauses in breathing support for up to 8 seconds, potentially affecting patient safety.
Draeger Medical recalls Babylog VN500 ventilators with CO2 measurement software 2.51 or lower. This version may cause brief pauses in breathing support for neonatal patients, risking loss of pressure support for up to 8 seconds.
Draeger Medical recalls Babylog VN800 ventilators from 2019-2020 due to software problems causing incorrect oxygen levels and ventilation restarts. Affected units may need repair or replacement.
Draeger Medical recalls Evita V800 ventilators from 2019-2020 with software issues that may cause incorrect oxygen levels or ventilation restarts. Affected units require immediate attention to prevent patient harm.
Draeger Medical recalls Evita V600 ventilators (2019-2020 models) due to software problems causing incorrect oxygen alarms and ventilation restarts. Affected units may need repair or replacement.
Draeger Medical recalls Babylog VN600 ventilators from 2019-2020 due to software problems causing incorrect oxygen alarms and ventilation restarts. Affected units may need repair or replacement.
Draeger Medical recalls VentStar Basic (N) 180 breathing circuits due to risk of Y-piece detachment causing ventilation leaks. All units are affected.
Draeger recalls VentStar Anesthesia 180 breathing circuits due to potential Y-piece detachment causing ventilation leaks. All units are affected. Contact for return instructions.
Draeger Medical recalls VentStar Watertrap 180 breathing circuits due to potential detachment causing breathing leaks. All units are affected; contact for remedy.
Draeger Medical recalls ID Circuit Basic (N) 180 breathing circuits due to potential detachment causing ventilation leaks. All units are affected. Contact for replacement.
Draeger Medical recalls VentStar Anesthesia WT(P) 180 breathing circuits without water traps due to potential short circuit from incorrect assembly. These single-use sets may cause electrical issues during anesthesia procedures.
Draeger Medical recalls ID Circuit Basic 250 breathing circuits without water traps due to potential short circuits from incorrect assembly. These single-use anesthesia sets may cause electrical issues during medical procedures.
Draeger Medical recalls VentStar Basic 180 breathing circuits without water traps due to potential short circuits. These single-use sets may cause incorrect connections or electrical issues during anesthesia delivery.
Draeger Medical recalls VentStar Basic 180 breathing circuits without water traps due to potential short circuits. These single-use sets may cause incorrect connections or electrical issues during anesthesia.
Draeger Medical recalls VentStar Basic 25:00 breathing circuits without water traps due to potential short circuits. These single-use anesthesia sets may cause incorrect connections or electrical issues during use.
Draeger Medical recalls ID Circuit Watertrap 18:00 (P) 180 breathing circuits without water traps due to potential short circuits. All units are affected.
Draeger Medical recalls VentStar Basic 250 breathing circuits without water traps due to potential short circuits. These single-use sets risk incorrect connections and electrical issues. Affected units lack water traps for condensate collection.
Draeger Medical recalls VentStar Watertrap 18:00 (P) 180 breathing circuits without water traps due to potential incorrect connections causing short circuits. All units are affected.
Draeger Medical recalls ID Circuit Basic 180 breathing circuits without water traps due to potential short circuits. These single-use anesthesia sets may cause incorrect connections or electrical issues during use.
Draeger Medical recalls Apollo anesthesia machines (cat. 8605310) due to potential risk of delivering 100% N2O causing patient hypoxia. Affected units may need immediate action to prevent serious injury.
Draeger Medical recalls Fabius GS MRI anesthesia machines due to potential risk of hypoxic patient mixtures from N2O dosing errors. This could lead to patient death if a fault occurs in the S-ORC module.
Draeger recalls Fabius GS Premium anesthesia machines (cat. 8607000) due to potential risk of hypoxic patient mixtures from N2O dosing errors. This could lead to serious harm or death during surgery.
Draeger Medical recalls Fabius GS Tiro anesthesia machines (cat. 8606000) due to potential risk of hypoxic patient mixtures from faulty N2O dosing. This could lead to serious injury or death during surgery.
Draeger Medical recalls Perseus A500 anesthesia machines due to potential risk of delivering 100% nitrous oxide, which could cause patient hypoxia and death. Affected units have specific model numbers and were sold for medical use.
Draeger Medical recalls specific Carina Ventilators due to potential breathing gas contamination from corroded valve assemblies. Affected units have serial numbers starting with ASKM or ASKN. Contact for remedy details.
