Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics — Class II medical device recall Z-2084-2013
Terminated recall by Respironics California Inc, reported 2013-09-04, distributed nationwide. The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making t
| Recall number | Z-2084-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Respironics California Inc, Carlsbad, CA, United States |
| Recall initiated | 2007-10-29 |
| Classified | 2013-08-26 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2013-08-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AU, BD, BR, CA, CL, CO, DE, DZ, EC, EG, ES, FR, GB, GT, HK, IN, IT, JP, KR, MX, MY, PE, PH, PK, RU, TH, TR, TW, VE, VN, ZA |
| Model numbers | V1000 |
Product
Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
Reason for recall
The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark and making the display unreadable.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2084-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.