Quick Facts at a Glance
- Recall Date
- November 24, 2025
- Hazard Level
- HIGH
- Brand
- Draeger
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Draeger
- Product type
- Anesthetic Vaporizer
- Model numbers
- Model No. M36500, UDI-DI: 04048675301363, Serial No. ASUK-1181, ASUK-1186, ASUK-1187, ASUK-1196, ASUK-1197, ASUK-1198 +12 more
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 24, 2025
Reported by FDA DEVICE
December 31, 2025
RecallRadar source check
January 7, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
A certain component of affected devices was not delivered within specification and contained impurities.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Draeger, Inc. or your healthcare provider for instructions. Notification method: Letter
About This Product
The Draeger Vapor 3000 is an unheated, calibrated anesthetic vaporizer used in medical settings for delivering anesthetic gases to patients. Healthcare providers typically use this device during surgical procedures to ensure patient safety.
Why This Is Dangerous
The vaporizer is recalled due to a component that contains impurities and does not meet the required specifications, which may compromise patient safety during anesthesia delivery.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall may cause disruption in medical settings that rely on the Draeger Vapor 3000 for anesthetic administration, potentially delaying procedures and impacting patient care.
Practical Guidance
How to identify if yours is affected
- Check the model number on your device to see if it is M36500.
- Review the list of serial numbers associated with the recall.
- Contact Draeger, Inc. if you are uncertain about your device's status.
Where to find product info
The model number and serial numbers are usually located on the device's label or in the product documentation.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks.
If the manufacturer is unresponsive
- Document your communications with Draeger, Inc.
- Follow up with customer service if you do not receive a response within a week.
- Consider filing a complaint with the FDA if issues persist.
How to prevent similar issues
- Always check for recalls on medical devices before use.
- Ensure devices have necessary certifications and meet safety standards.
- Consult healthcare professionals for alternative devices if recalls are announced.
Documentation advice
Keep records of your purchase, correspondence with Draeger, and any incident reports related to the device.
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Product Details
The recall affects the Draeger Vapor 3000 anesthetic vaporizer, model number M36500. These devices were distributed worldwide, including across 13 U.S. states such as California and New York. The quantity recalled is 188 units.
Key Facts
- Recall date: November 24, 2025
- 188 units recalled globally
- Impurities in a critical component
- Class I recall indicates high risk
- Immediate cessation of use required
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Safety Guide
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