Inogen, Inc Portable Oxygen Generator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Portable Oxygen Generator
Brand
Inogen, Inc
Lot Codes / Batch Numbers
All codes.
Products Sold
All codes.
Inogen, Inc is recalling Portable Oxygen Generator due to Firm plans to upgrade all units to correct situations that could lead to interuption in oxygen delivery.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm plans to upgrade all units to correct situations that could lead to interuption in oxygen delivery.
Recommended Action
Per FDA guidance
Recall is scheduled to begin August 1st 2005 by letter to customers informing them that the units will be upgraded on a predetermined schedule. Firm estimates completion in 6 months.
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 noticePage updated: Jan 10, 2026