FDA Medical Device Recalls (openFDA)
Ross Products Division Abbott Laboratories: The Companion ClearStar Pump System, for enteral feeding.
- Recall number
- Z-1142-2007
- Recalling firm
- Ross Products Division Abbott Laboratories
- Product
- The Companion ClearStar Pump System, for enteral feeding.
- Status
- Terminated
- Initiated
- 2007-06-21
- Posted
- 2007-08-07
- Terminated
- 2012-09-26
- Reason
- The transducer adapter bracket on the pump could crack or break and potentially result in under delivery of the enteral product.
- Root cause
- Equipment maintenance
- Action
- Consignees were notified by letter dated 6/25/2007. A revised letter was sent 07/26/2007.
- Quantity
- 27,814
- Distribution
- Worldwide, including USA and Canada.
- Lot, serial or model codes
- List #55238 & 55239
- 510(k) numbers
- K981541
- PMA numbers
- not on file
- Product code
- LZH
- Firm FEI
- 1000136098
- Firm city
- Columbus
- Firm state
- OH
- 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
- 2026-10-14
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