FDAFDA · Food and drugs·Recall number Z-2084-2013
Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
Published September 4, 2013 · Recall initiated: October 29, 2007
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Respironics California Inc
- Distributor
- USA Nationwide and Worldwide to Algeria, Argentina, Australia, Bangladesh, Brazil, Cambodia, Canada, Chile, Colombia, Ecuador, Egypt, France, Germany, Guatemala, Hong Kong, India, Italy, Japan, Libya, Malaysia, Mexico, Pakistan, Peru, Philippines, Puerto Rico, Russia, South Africa, South Korea, Spain, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Venezuela, and Vietnam.
- Lot
- Model Number: V1000
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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