FDA Medical Device Recalls (openFDA)
Inogen, Inc: Portable Oxygen Generator
- Recall number
- Z-1368-05
- Recalling firm
- Inogen, Inc
- Product
- Portable Oxygen Generator
- Status
- Terminated
- Initiated
- 2005-08-01
- Posted
- 2005-08-12
- Terminated
- 2007-02-13
- Reason
- Firm plans to upgrade all units to correct situations that could lead to interuption in oxygen delivery.
- Root cause
- Other
- Action
- 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.
- Quantity
- 900
- Distribution
- Nationwide
- Lot, serial or model codes
- All codes.
- 510(k) numbers
- ["K032818"]
- PMA numbers
- not on file
- Product code
- CAW
- Firm FEI
- 3004672275
- Firm city
- Goleta
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28