Sorenson Medical, Inc. ambIT Ambulatory Infusion Therapy Intermittent Pump Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ambIT Ambulatory Infusion Therapy Intermittent Pump
Brand
Sorenson Medical, Inc.
Lot Codes / Batch Numbers
Catalog Number: 220245. All serial numbers.
Products Sold
Catalog Number: 220245. All serial numbers.
Sorenson Medical, Inc. is recalling ambIT Ambulatory Infusion Therapy Intermittent Pump due to Intermittent Infusion pump may continually dispense medication under certain conditions.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Intermittent Infusion pump may continually dispense medication under certain conditions.
Recommended Action
Per FDA guidance
All direct accounts were contacted by email and phone on 05/03/2006. Distributors were instructed to identify end users for Recalling Firm notification
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL, KS, NJ, PA, WA
Page updated: Jan 10, 2026