Drugs & medicalClass I

Draeger, Inc. recalls Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.

A certain component of affected devices was not delivered within specification and contained impurities.

Read the official notice →
Date
2025-12-31
Country
United States
Brand
Draeger
Product
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
Classification
Class I
Units
Worldwide - US Nationwide distribution in the states of AK, CA, FL, IA, KS,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Draeger recalls

  1. 2026-10-07
  2. US
    Drugs & medicalClass I

    Draeger, Inc. recalls VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a resuscitation module.

    Potential cracks in the hose, which could lead to leakage or the hose falling off.

    FDA · DeviceDraeger, Inc.US Nationwide distribution including in the states of IN, AK, AL, AZ, CA, CO,…Official notice →
  3. 2026-06-10
  4. US
    Drugs & medicalClass I

    Draeger, Inc. recalls Atlan A350XL. Model Number: 8621600. anesthesia workstation

    The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

    FDA · DeviceDraeger, Inc.US distribution in WI, AR, MN, WI, CO, MA, PA, AZ, FL, NY, SD, ND.…Official notice →
  5. 2025-12-17
  6. US
    Drugs & medicalClass I

    Draeger, Inc. recalls ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the breathing system and the…

    Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

    FDA · DeviceDraeger, Inc.Worldwide distribution. US states of CA, FL, IL, NY, OH, OK, PA, SC, TX, and…Official notice →
  7. 2025-10-08
  8. US
    Drugs & medicalClass I

    Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product Description: The Atlan…

    The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

    FDA · DeviceDraeger, Inc.Devices were imported from Draegerwerk Ag and Co. KGaA and distributed in the…Official notice →
  9. 2025-08-06
  10. US
    Drugs & medicalClass I

    Draeger, Inc. recalls SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

    Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.

    FDA · DeviceDraeger, Inc.Worldwide - US Nationwide distribution including in the states of AK, AZ, CA,…Official notice →
  11. 2025-04-09
  12. US
    Drugs & medicalClass I

    Draeger, Inc. recalls Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description:…

    The potential for cracks forming in the breathing circuit hose.

    FDA · DeviceDraeger, Inc.Domestic: Nationwide Distribution. International - following countries:…Official notice →
All 7 Draeger recalls →

Other drugs & medical recalls in the United States

  1. 2025-12-31
  2. US
    Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR)…

    When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.

    FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide and the countries of Canada, Germany,…Official notice →
  3. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis…

    Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to…

    FDA · DeviceCareFusion 303, Inc.Worldwide - US Nationwide distribution including in the states of CO, IN, OH,…Official notice →
  4. US
    Drugs & medicalClass I

    Alcon Research LLC recalls Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Numbers: 9903-20, 17188-04, 19762-03, 19203-04, 19203-04,…

    Ophthalmic procedure packs may have incomplete seals affecting sterility.

    FDA · DeviceAlcon Research LLCUS Nationwide distribution in the states of CA, ND, UT.Official notice →
  5. US
    Drugs & medicalClass II

    AGFA Healthcare Corp. recalls Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common Name: DR 800

    It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on the NX workstation when ABS is not enabled.

    FDA · DeviceAGFA Healthcare Corp.U.S. Nationwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    Merck Sharp & Dohme LLC recalls Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ…

    Presence of particulate matter: potential presence of metal particulates in the product.

    FDA · DrugMerck Sharp & Dohme LLCNationwide in the USAOfficial notice →
  7. 2025-12-24
  8. US
    Drugs & medicalClass II

    Abbott Laboratories recalls Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20

    Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues found in the Alinity ci-series…

    FDA · DeviceAbbott LaboratoriesWorldwide distribution: US (nationwide) to states of: AK, AL, AR, AZ, CA, CO,…Official notice →
See all drugs & medical recalls →