Draeger Medical, Inc. recalls
Every recall we track for Draeger Medical, Inc. — 64 in all, from 2018–2024 — plus the complaints and injury reports the public filed about them. 9 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Draeger Medical, Inc. dropped to zero in 2025 (0, down from 5 in 2024). 14% rated “stop using now”.
All FDA recall records for Draeger Medical, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 5 | 13 | 0 | 1 | 19 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 4 | 7 | 0 | 0 | 11 |
| 2022 | 0 | 0 | 1 | 2 | 3 |
| 2023 | 0 | 23 | 2 | 1 | 26 |
| 2024 | 0 | 5 | 0 | 0 | 5 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Draeger Medical, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Draeger Medical, Inc. recalls
17 shown- Use cautionMedical device
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component:
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.
DraegerOct 15, 2024 - Use cautionMedical device
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation
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.
DraegerOct 15, 2024 - Use cautionMedical device
Draeger Medical, Inc. recalls Dr¿ger Perseus A500 Anesthesia Workstation
Draeger Medical recalls Perseus A500 anesthesia workstations that may unexpectedly shut down on battery power, risking patient safety during surgery.
DraegerMar 20, 2024 - Lower riskMedical device
Draeger Medical, Inc. recalls Carina Sub-Acute Care Ventilator
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 MedicalJul 12, 2023 - Use cautionMedical device
Draeger Medical, Inc. recalls Oxylog 3000 Plus emergency and transport ventilator
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.
DraegerJun 12, 2023 - Use cautionMedical device
Draeger Medical, Inc. recalls VentStar Basic (P)180, MP00351
Draeger Medical recalls VentStar Basic (P)180 ventilators due to risk of breathing circuit pieces detaching during use, potentially causing breathing issues.
Draeger MedicalApr 17, 2023 - Lower riskMedical device
Draeger Medical, Inc. recalls NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)
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 MedicalJan 23, 2023 - UnratedMedical device
Draeger Medical, Inc. recalls Drager SafeStar 55, Catalog No. MP01790
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 MedicalMay 16, 2022 - UnratedMedical device
Draeger Medical, Inc. recalls Evita V500 Ventilator with Software 2.51.01 and Lower - intended for the ventilation of adult, pediatric and neonatal
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.
DraegerFeb 14, 2022 - Use cautionMedical device
Draeger Medical, Inc. recalls Draeger Fabius MRI Anesthesia Machine, Catalog Number 8607300
Draeger recalls 26 Fabius MRI Anesthesia Machines with oxygen flow control error that may cause patient oxygenation issues if central oxygen pressure is unstable.
DraegerDec 16, 2021 - Use cautionMedical device
Draeger Medical, Inc. recalls Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for the ventilation of neonatal patients from
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 MedicalSep 10, 2021 - Use cautionMedical device
Draeger Medical, Inc. recalls Critical Care Ventilator, Catalog Number(s): 8422200: Babylog VN600 - Product Usage: used for treating patients who
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 MedicalApr 16, 2021 - Stop using nowMedical device
Draeger Medical, Inc. recalls ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing
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 MedicalJan 29, 2021 - Use cautionMedical device
Draeger Medical, Inc. recalls ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit
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 MedicalDec 21, 2018 - Stop using nowMedical device
Draeger Medical, Inc. recalls Perseus A500 Anesthesia Machine; Cat. no. MK06000 Product V Product Usage: Intended for use in anesthetizing adults,
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.
DraegerMay 24, 2018 - Use cautionMedical device
Draeger Medical, Inc. recalls Carina Ventilator, ventilator. Catalog no. 5704110. Long-term ventilator for treatment in hospitals by a qualified
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.
Draeger MedicalApr 26, 2018 - Use cautionMedical device
Draeger Medical, Inc. recalls Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for
Draeger Medical recalls Fabius MRI anesthesia machines (serial numbers ASKM-0020, ASKM-0011, etc.) due to potential ventilation failure if motor position detection is disturbed or cover is damaged. This could affect patient safety during surgery.
Draeger MedicalMar 1, 2018
Draeger Medical, Inc. recall questions
How many recalls has Draeger Medical, Inc. had?
64 recalls from Draeger Medical, Inc. are on record with U.S. safety agencies, from 2018–2024.
What is the most recent Draeger Medical, Inc. recall?
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component:, dated Oct 15, 2024. Every Draeger Medical, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Draeger Medical, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Draeger Medical, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.