Respironics California Inc Esprit Ventilator. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Esprit Ventilator.
Brand
Respironics California Inc
Lot Codes / Batch Numbers
Serial numbers: VS300430, VS3004361, VS3004335, VS3004301, VS3004327, VS3004353, VS3004377, VS3004366, VS3004328, VS3004337, VS3004357, VS3004385, VS3004369, VS3004295, VS3004310, VS3004292, VS3004305, VS3004381, VS3004296, VS3004299.
Products Sold
Serial numbers: VS300430, VS3004361, VS3004335, VS3004301, VS3004327, VS3004353, VS3004377, VS3004366, VS3004328, VS3004337, VS3004357, VS3004385, VS3004369, VS3004295, VS3004310, VS3004292, VS3004305, VS3004381, VS3004296, VS3004299.
Respironics California Inc is recalling Esprit Ventilator. due to Valves may stick in the closed position due to manufacturing error.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Valves may stick in the closed position due to manufacturing error.
Recommended Action
Per FDA guidance
Uninstalled ventilators were returned for change of the inhalation module. Otherwise, service technicians replaced the module in the field. Recall is complete.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CO, GA, IL, MI, NJ, NY, NC, OH, PA
Page updated: Jan 10, 2026