Esprit V1000 and V200 Ventilators — Class I medical device recall Z-0008-2015
Terminated recall by Respironics California Inc, reported 2014-10-29. A failure of a specific component may prevent the ventilators from operating on AC power or transitioning back
| Recall number | Z-0008-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Respironics California Inc, Carlsbad, CA, United States |
| Recall initiated | 2014-09-17 |
| Classified | 2014-10-21 |
| Reported by FDA | 2014-10-29 |
| Terminated | 2016-09-28 |
| Countries outside the US | AR, CN, EG, HK, HN, ID, IL, IN, IQ, IT, JO, KR, LK, MX, MY, NG, NL, NP, PE, PH, PK, RS, SG, TH, VN, ZA |
| Serial numbers | 123600002, 123600005, 123600011, 123600015, 123600018, 123600023, 123600025, 123600029, 123600030, 123600035, 123600036, 123600038, 123600039, 123600040, 123600042, 123600044, 123600045, 123600049, 123600053, 123600056, 123600059, 123600063, 123600077, 123600078, 123600080 and 475 more |
| Model numbers | V1000, V200 |
Product
Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Generation Power Supply Repair Part (RP)Kits Microprocessor-controlled, electrically powered mechanical ventilators intended for use by qualified medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients as prescribed by a physician.
Reason for recall
A failure of a specific component may prevent the ventilators from operating on AC power or transitioning back to AC power when operating on battery. Additionally, if a battery is not present or is depleted the ventilators will not operate. This failure will cause the loss of ventilator support, which may result in hypercarbia or hypoxemia.
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-0008-2015. 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.