This site contains information on Vapotherm Inc's voluntary recall of the Vapotherm 2000i humidification device. As part of this voluntary recall and upon receipt at Vapotherm, Inc., devices will undergo a high-level disinfection process. Subsequent to this recall, comprehensive instructions for product disinfection and device use will be provided to the customer with disinfected Vapotherm 2000i units. The information provided with the returned device will also include recommendations for use of single patient disposable components, recommended frequency of cleaning and guidelines for changing the Vapor Transfer Cartridge. In addition, new components will be made available to allow for the use of sterile water with the system and instructions provided for ensuring a closed system is maintained in the patient care environment.
Notification Process:
An official notification will be mailed to your hospital via U.S. Mail.
To Request Instructions for Returning 2000i Units to Vapotherm:
To request instructions for return of 2000i units click the link below and complete the form. You will be contacted by email or phone with instructions for timing, shipping and any other necessary information.
Recall Form