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Respironics California Inc: Medical Device Recalls in 2014

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Respironics California Inc in 2014. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2012
2013
2014
2017
  • 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.
  • 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.
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