Z-0741-03

Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)

Name: Z-0741-03 Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)
Creator: I-Flow Corporation
Published: 2003-03-18
License: https://open.fda.gov/license/

Halyard Health / initiated 2003-03-18 / Terminated

FDA source

I-Flow Corporation began a recall of Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr) on 2003-03-18. The reason FDA records is "Overinfusion due to misassembly". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0741-03
Status: Terminated
Initiated: 2003-03-18
Posted: 2003-04-18
Terminated: 2003-11-20
Recalling firm: Halyard Health
Product: Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)
Reason for recall: Overinfusion due to misassembly.
FDA root cause: Other
Action: 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.
Quantity in commerce: 2638 units
Distribution: Only in France to distributor B. Braun Medical, France
Product codes and lots: Lot numbers 04434366/2A2469 and 04434367/2A2470.

K991513Class IIHomepump C-Series and Homepump C-Series One-Step KvoI-Flow Corp. / cleared 1999-06-21

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)