FDA Medical Device Recalls (openFDA)
Kinetic Concepts, Inc: TriaDyne I and TriaDyne II Powered Adjustable Hospital Beds
- Recall number
- Z-0748-03
- Recalling firm
- Kinetic Concepts, Inc
- Product
- TriaDyne I and TriaDyne II Powered Adjustable Hospital Beds
- Status
- Terminated
- Initiated
- 2000-04-11
- Posted
- 2003-04-18
- Terminated
- 2003-12-16
- Reason
- Battery Failure/ Outgassing
- Root cause
- Other
- Action
- Service centers were notified of the new battery maintenance policy on 4/11/2000 in a Technical Bulletin and again on 9/11/2000. Non-service center customers were notified by letter in October 2002.
- Quantity
- 915 units
- Distribution
- Nationwide
- Lot, serial or model codes
- All Serial Numbers
- 510(k) numbers
- not on file
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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