FDA Medical Device Recalls (openFDA)
Ross Products Division Abbott Laboratories: Embrace Enteral Pump
- Recall number
- Z-1141-2007
- Recalling firm
- Ross Products Division Abbott Laboratories
- Product
- Embrace Enteral Pump
- Status
- Terminated
- Initiated
- 2007-06-21
- Posted
- 2007-08-08
- Terminated
- 2012-09-20
- Reason
- Continued use of the pump may cause the door pivot point on the back of the pump to crack or break. This will cause the pump to shut down and stop the initiation of enteral feeding.
- Root cause
- Equipment maintenance
- Action
- Consignees were notified by letter dated 6/25/2007. The firm sent a revised letter on 07/26/2007.
- Quantity
- 9,600 units
- Distribution
- The product was distributed throughout the US.
- Lot, serial or model codes
- List #55335 & 55336
- 510(k) numbers
- ["K031407"]
- 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
- 2026-10-06
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