Respironics California Inc Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
Brand
Respironics California Inc
Lot Codes / Batch Numbers
Model Number: V1000
Products Sold
Model Number: V1000
Respironics California Inc is recalling Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000 due to The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.
Recommended Action
Per FDA guidance
A Medical Device Field Correction letter dated 10/26/2007 was sent to all customers who received the Esprit Ventilator. The recall letter informed the customers of the problems identified and the actions to be taken. Customers with questions are instructed to contact Respironics' Customer Service Dept. at (800) 345-6443, select Option#5, then select Option #4.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026