Data Foundry

Medical device recalls 2014

Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The… — Class II medical device recall Z-0485-2015

Terminated recall by Respironics California Inc, reported 2014-12-03, distributed nationwide. If the power supply fan mounting screws are installed incorrectly, the ends of the screws may touch the power

Recall numberZ-0485-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRespironics California Inc, Carlsbad, CA, United States
Recall initiated2014-10-29
Classified2014-11-27
Reported by FDA2014-12-03
Terminated2016-06-07
DistributedNationwide (US)
Countries outside the USAE, AR, AU, BG, BR, CA, CL, CN, CO, EC, EG, ES, GB, GR, HK, IN, IT, KR, LB, MX, MY, PA, PE, PH, PK, SA, SG, TH, TR, TW, VE, VN, ZA
Serial numbersVS3000536, VS3000538, VS3000542, VS3000553, VS3000563, VS3000570, VS3000574, VS3000576, VS3000584, VS3000604, VS3000614, VS3000631, VS3000637, VS3000638, VS3000641, VS3000644, VS3000675, VS3000918, VS3000921, VS3000922, VS3000923, VS3000924, VS3000927, VS3000930, VS3000931 and 475 more

Product

Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators are microprocessor-controlled, electrically powered mechanical ventilators. Intended for use by medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients.

Reason for recall

If the power supply fan mounting screws are installed incorrectly, the ends of the screws may touch the power supply printed circuit board assembly (PCBA) and short to ground. This may prevent the ventilator to switch to battery power if AC power is disrupted.

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-0485-2015. 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.