Device Recall Penlon Sigma Delta Vaporizer

  • Model / Serial
    All; recalled products are traced by serial numbers D0312-XXXX to D1112-XXXX.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including FL, KY, PA, ND, MN, IL, NJ, TX, TN, and VA. Internationally to Belgium, China, Czech Republic, France, Germany, Switzerland, Australia, Finland, Holland, Lithunia, Malta, Poland, and Slovakia.
  • Product Description
    Delta Vaporizer || An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Penlon, Ltd., Abingdon Science Park, Barton Lane, Abingdon United Kingdom
  • Manufacturer Parent Company (2017)
  • Source
    USFDA