Anesthetic Vaporizer Recall: Draeger Removes Vapor 2000 And Vapor 3000 Vaporizers
Recall Summary Draeger is recalling certain Vapor 2000 and Vapor 3000 anesthetic vaporizers due to impurities discovered in one of the device components. These vaporizers are used in medical settings to deliver anesthesia during procedures. The recall affects healthcare facilities and surgical centers that use these specific models.
- Recalling firm
- Anesthetic Vaporizer Recall
- Product
- Draeger is removing certain Vapor 2000 and Vapor 3000 Vaporizers due to impurities found within a component.
- Reason
- Draeger is removing certain Vapor 2000 and Vapor 3000 Vaporizers due to impurities found within a component.
- Category
- drug recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-01-16
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/12b326ba-be17-4cea-b25b-26441399e576