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Draeger Vapor 3000 Anesthetic Vaporizer Recalled Due to Impurities

Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.

Official notice
DraegerHealth & Personal CareMedical DevicesModel No. M36500UDI-DI: 04048675301363Serial No. ASUK-1181

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
November 24, 2025
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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.

  1. Recall announced

    November 24, 2025

  2. Reported by FDA DEVICE

    December 31, 2025

  3. RecallRadar source check

    January 7, 2026

  4. 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

  1. Check the model number on your device to see if it is M36500.
  2. Review the list of serial numbers associated with the recall.
  3. 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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Brand
Model Numbers
Model No. M36500
UDI-DI: 04048675301363
Serial No. ASUK-1181
ASUK-1186
ASUK-1187
+15 more
Affected States
ALL
Report Date
December 31, 2025
Recall Status
ACTIVE

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