Z-0585-06

Easypump L T 60-24 infusion pump

Name: Z-0585-06 Easypump L T 60-24 infusion pump
Creator: I-Flow Corporation
Published: 2006-01-17
License: https://open.fda.gov/license/

Halyard Health / initiated 2006-01-17 / Terminated / root cause: sterility

FDA source

I-Flow Corporation began a recall of Easypump L T 60-24 infusion pump on 2006-01-17. The reason FDA records is "The sterile pack may contain the wrong infusion pump inside". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as sterility.

Recall record

Recall number: Z-0585-06
Status: Terminated
Initiated: 2006-01-17
Posted: 2006-03-07
Terminated: 2007-02-05
Recalling firm: Halyard Health
Product: Easypump L T 60-24 infusion pump
Product code: MEB Pump, Infusion, Elastomeric
Reason for recall: The sterile pack may contain the wrong infusion pump inside.
Root cause tag: sterility
FDA root cause: Other
Action: The affected customer has been notified with a Notification letter dated January 17, 2006 via e-mail of Recall Notification Letter, with follow-up confirmation e-mails.
Quantity in commerce: 549
Distribution: France only
Product codes and lots: lot 562857

Product code MEB

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)