FDA Medical Device Recalls (openFDA)
Sorenson Medical, Inc.: ambIT Ambulatory Infusion Therapy Intermittent Pump
- Recall number
- Z-1188-06
- Recalling firm
- Sorenson Medical, Inc.
- Product
- ambIT Ambulatory Infusion Therapy Intermittent Pump
- Status
- Terminated
- Initiated
- 2006-05-03
- Posted
- 2006-07-01
- Terminated
- 2006-08-09
- Reason
- Intermittent Infusion pump may continually dispense medication under certain conditions.
- Root cause
- Other
- Action
- All direct accounts were contacted by email and phone on 05/03/2006. Distributors were instructed to identify end users for Recalling Firm notification
- Quantity
- 72 pumps
- Distribution
- Worldwide distribution (including-states of IL, KS, NJ, PA, WA. , countries of Germany, Malaysia, New Zealand, Slovenia.
- Lot, serial or model codes
- Catalog Number: 220245. All serial numbers.
- 510(k) numbers
- ["K033425"]
- PMA numbers
- not on file
- Product code
- FRN
- Firm FEI
- 1000117099
- Firm city
- West Jordan
- Firm state
- UT
- 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