---
title: "The failure occurs if a user on the Omnipod 5 iOS application selects and hol... — FDA record Z-0132-2026 | Is It on Recall"
description: "The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying f"
url: https://isitonrecall.com/recall/fda-device-z-0132-2026-the-failure-occurs-if-a-user-on-the-omnipod-5-ios-application-selects-and-holds-down-on-a-manual-ent/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magn... — FDA record Z-0132-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 11, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a single number on the keyboard.
- **Reason**: The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a single number on the keyboard. This causes the single digit number to duplicate. This could result in errors in manual entry of digits - examples: bolus entry, I:C ratio, bolus calculator, prior to starting the bolus insulin delivery. Therefore, this may result in over delivery of insulin which may cause hypoglycemia.
- **Classification**: Class II
- **Recalling firm**: Insulet Corporation
- **Quantity**: 174,013 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0132-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0132-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Omnipod 5 App Software. UDI: 10385083000459. All software versions 2.X.X |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Oct 22, 2025
- **Recall initiation date**: Sep 11, 2025
- **Center classification date**: Oct 10, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0132-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Insulet Corporation records](https://isitonrecall.com/brand/insulet-corporation/)
