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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66425

2 recalled-product records grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
September 27, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Insulet Corporation

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

OmniPod Insulin Management System Starter Kit; Model Reference Number: SKT-UST400 (Starter Kit) Product Usage: The Starter Kit (SKT-UST400) is provided to users as an introduction to the OmniPod Insulin Management System prior to initiating care. It includes the Personal Diabetes Manager (PDM) with two AAA alkaline batteries, a USB cable, a Users Guide, a Soft Carrying Case, a Troubleshooting guide, a Warranty Registration Card, and two Alcohol Pads. The OmniPod 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. The glucose measurements should not be used for the diagnosis of or screening for diabetes. The PDM glucose meter is intended for single-patient use and should not be shared. Abbott FreeStyle test strips are used with the built-in FreeStyle meter for the quantitative measurement of blood glucose in fresh whole capillary blood from the finger, upper arm and palm. Abbott Freestyle Control Solutions are used to verify that the meter and test-strips are working together properly and that the test is performed correctly.

Z-0165-2014
Recall number
Z-0165-2014
Initiated
September 27, 2013
Classification
Class II
Status
Terminated
Recalling firm
Insulet Corporation
Quantity
1,719 starter kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Alcohol Prep Pads contained within the kit are not properly labeled.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Alcohol Prep Pads contained within the kit are not properly labeled.

Code information

Lot Numbers: L13483, L13485, L13478, & L13481

Distribution pattern

Worldwide Distribution - USA Nationwide and the country of Israel.

device · product 2 of 2

OmniPod Insulin Management Product Demonstration Kit; Model Reference Number: (PDK-ZXP490) Product Usage: The Demonstration Kit (PDK-ZXP490) is an alternate kit provided to potential patients by healthcare professionals for patients to experience what wearing a Pod may feel like prior to purchase. Each Demonstration Kit includes a UST400 brochure, one Alcohol Pad, and a Pod. The OmniPod 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. The glucose measurements should not be used for the diagnosis of or screening for diabetes. The PDM glucose meter is intended for single-patient use and should not be shared. Abbott FreeStyle test strips are used with the built-in FreeStyle meter for the quantitative measurement of blood glucose in fresh whole capillary blood from the finger, upper arm and palm. Abbott Freestyle Control Solutions are used to verify that the meter and test-strips are working together properly and that the test is performed correctly.

Z-0166-2014
Recall number
Z-0166-2014
Initiated
September 27, 2013
Classification
Class II
Status
Terminated
Recalling firm
Insulet Corporation
Quantity
5,050 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Alcohol Prep Pads contained within the kit are not properly labeled.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Alcohol Prep Pads contained within the kit are not properly labeled.

Code information

Lot Numbers: L13470

Distribution pattern

Worldwide Distribution - USA Nationwide and the country of Israel.

Field note

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