D-Vapor 3000 M36700Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048675301370), received between May 17, 2024 and May 17, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

1 other recall cover devices cleared under the same FDA submission (K042276); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 17, 2024Fluid/Blood Leak; Detachment of Device or Device Component; Fluid/Blood Leak; Detachment of Device or Device Component

  IT WAS REPORTED THAT - DURING FILLING THE VAPORIZER WITH ANESTHETIC AGENT - THE SUBSTANCE WAS RELEASED AND TWO PERSONS WERE EXPOSED. CURRENTLY, IT CANNOT BE EXCLUDED THAT MEDICAL INTERVENTION WAS REQUIRED TO PREVENT FROM SERIOUS INJURY AND THUS, THIS REPORT IS FILED IN ABUNDANCE OF CAUTION.

  Patient problems: Insufficient Information

  MAUDE report 19339054 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042276. One submission often covers many models, so check the product and lot details in each record.

• Z-1812-2016 · Apr 21, 2016 · Terminated
  Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and Bottles. Catalog # M35500 (D-Vapor) and M36700 (D-Vapor 3000). Anesthesia Vaporizer