FDA Medical Device Recalls (openFDA)
Kinetic Concepts, Inc: KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas
- Recall number
- Z-0583-05
- Recalling firm
- Kinetic Concepts, Inc
- Product
- KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas
- Status
- Terminated
- Initiated
- 2003-06-06
- Posted
- 2005-03-10
- Terminated
- 2008-04-01
- Reason
- Weld failure causes side rail welds to turn upside down or break off of the bed.
- Root cause
- Other
- Action
- The firm initiated the recall by telephone on 06/06/2003. The firm has inspected and corrected the beds.
- Quantity
- 1181 beds
- Distribution
- The beds were distributed nationwide and to Brazil.
- Lot, serial or model codes
- Serial Numbers KASK00001 through KASK01212
- 510(k) numbers
- ["K970468"]
- PMA numbers
- not on file
- Product code
- IOQ
- 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