FDA Device recall Z-2084-2013
Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
- FDA Device
- Class II
- terminated
- Published 2013-09-04
On 2013-09-04 the FDA classified a Class II recall of Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000 by Respironics California, citing the power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2084-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2007-10-29 |
| Published | 2013-09-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Respironics California |
| Distribution | US |
Product
Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
Reason
The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.
Identifiers
| code_info | Model Number: V1000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2084-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.