I-Flow Corporation Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr) Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)
Brand
I-Flow Corporation
Lot Codes / Batch Numbers
Lot numbers 04434366/2A2469 and 04434367/2A2470.
Products Sold
Lot numbers 04434366/2A2469 and 04434367/2A2470.
I-Flow Corporation is recalling Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr) due to Overinfusion due to misassembly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Overinfusion due to misassembly.
Recommended Action
Per FDA guidance
Recall letter was sent to sole distributor, B Braun FRance by email on 3/18/2003. Return of stock and subrecall was requested. Consignee has acknowledged implementing subrecall.
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
IN
Page updated: Jan 10, 2026