Draeger, Inc. recalls
Every recall we track for Draeger, Inc. — 22 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Draeger, Inc. peaked in 2025 (19); 22 since 2017. 5% rated “stop using now”.
All FDA recall records for Draeger, 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 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 5 | 13 | 1 | 19 |
| 2026 (to date) | 1 | 2 | 0 | 0 | 3 |
Most common reasons for Draeger, Inc. recalls
What to do if you have a recalled Draeger, 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, Inc. recalls
7 shown- Stop using nowMedical device
Draeger, Inc. recalls VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a
Draeger recalls 1,063,643 VentStar Resus Neo neonatal breathing circuits due to potential hose cracks causing leakage or disconnection. Stop using immediately.
DraegerSep 3, 2026 - Use cautionMedical device
Draeger, Inc. recalls Atlan A350XL. Model Number: 8621600. anesthesia workstation
Draeger recalls Atlan A350XL anesthesia workstations with model 8621600 due to potential piston ventilator failure before use or mechanical ventilation failure during use. Affected units have specific serial numbers listed in the recall notice.
DraegerMay 7, 2026 - Lower riskMedical device
Draeger, Inc. recalls Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
Draeger recalls unheated anesthetic vaporizers with specific serial numbers due to impure components that may not meet calibration standards. Affected units include models M35054 with serial numbers starting ASUK-0421 to ASUK-1532.
DraegerNov 24, 2025 - Use cautionMedical device
Draeger, Inc. recalls ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the
Draeger recalls ErgoStar CM 60 airway connectors with model MP01860 due to reported hose cracks that could cause injury during mechanical ventilation.
DraegerNov 10, 2025 - Use cautionMedical device
Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product
Draeger Inc. recalls Atlan A350 anesthesia workstations with model 8211500 due to potential piston ventilator failure before use or mechanical ventilation failure during use.
AtlanSep 9, 2025 - Lower riskMedical device
Draeger, Inc. recalls SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
Draeger recalls SafeStar 90 Plus filters due to potential CO2 curve increases during gas sampling. Affected units include all lots of model MP05785.
DraegerJun 16, 2025 - Lower riskMedical device
Draeger, Inc. recalls Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable
Draeger Inc. recalls VentStar Flex 220 breathing circuits (model MP00355) due to potential cracking. This could lead to breathing gas leaks during use. Affected units were sold starting in 2020.
VentStarMar 12, 2025
Draeger, Inc. recall questions
How many recalls has Draeger, Inc. had?
22 recalls from Draeger, Inc. are on record with U.S. safety agencies, from 2025–2026.
What is the most recent Draeger, Inc. recall?
Draeger, Inc. recalls VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a, dated Sep 3, 2026. Every Draeger, Inc. recall is listed on this page, newest first.
Why are Draeger, Inc. products recalled?
The most common reasons on record: The potential for cracks forming in the breathing circuit hose. (7).
What should I do if I have a recalled Draeger, 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, 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.