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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 72535

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

Open FDA event record

Event summary

Timeline bucket
November 02, 2015
Product types
Device
Classifications
Class I
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 (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
Recall number
Z-0393-2016
Initiated
November 02, 2015
Classification
Class I
Status
Terminated
Recalling firm
Insulet Corporation
Quantity
26,230.9 boxes

App-derived interpretation

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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

device · product 2 of 2

OmniPod¿, Insulin Management System (OUS) Catalog Number: 14810 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-0394-2016
Recall number
Z-0394-2016
Initiated
November 02, 2015
Classification
Class I
Status
Terminated
Recalling firm
Insulet Corporation
Quantity
5,179.0 boxes

App-derived interpretation

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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Codes: L41908, L41910, F41935

Distribution pattern

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