FDANovember 2, 2015device

OmniPod¿, Insulin Management System (US) Catalog Number: PODZXP420 Product Usage: The OmnniPod¿ Insulin Management System is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin and for the quantitative measur...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Pod's needle mechanism fails to deploy or there is a delay in the deployment of the needle mechanism.

What to do

FDA enforcement status: Terminated

Brands named

insulet

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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