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Recall Observatory FDA recall evidence

Device product

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 measurement of glucose in fresh whole capillary blood (in vitro) from the finger.

Z-0393-2016

November 02, 2015

Class I

Product summary

Firm
Insulet Corporation
Event
Event 72535
Status
Terminated
Classification
Class I
Quantity
26,230.9 boxes
Official record key
device-enforcement:Z-0393-2016

Official wording

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

Code information: Lot Codes: L41880, L41881, L41892, L41895,L41897,L41898, L41899,L41900, L41901, L41902, L41903, L41904, L41905, L41906, L41907

Distribution pattern: Worldwide Distribution - US Nationwide and countries of Switzerland, Germany, and Israel.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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