FDA Medical Device Recalls (openFDA)
Kinetic Concepts, Inc: TransportAir, Accessory to an Air Bed, Auxiliary Blower Unit, manufactured by Kinetic Concepts, Inc.
- Recall number
- Z-0718-03
- Recalling firm
- Kinetic Concepts, Inc
- Product
- TransportAir, Accessory to an Air Bed, Auxiliary Blower Unit, manufactured by Kinetic Concepts, Inc.
- Status
- Terminated
- Initiated
- 1997-06-01
- Posted
- 2003-04-10
- Terminated
- 2003-07-08
- Reason
- Battery out-gassing due to battery over charging and/or secondary failure mode of deep-discharge.
- Root cause
- Other
- Action
- In approximately November 1997 the firm implemented the TransportAir retrograde for all active units.
- Quantity
- 4264
- Distribution
- Nationwide
- Lot, serial or model codes
- Serial numbers 0550037 through 0559399.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- INX
- Firm FEI
- 1625774
- Firm city
- San Antonio
- Firm state
- TX
- 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