---
title: "Easy Read App associated with First Response Pregnancy Test Sticks - Intended... — FDA record Z-1350-2023 | Is It on Recall"
description: "Church & Dwight First Response Pregnancy Kits was marketed with the Easy Read App without a new 510k. There is also a potential for Easy Read App to be unable t"
url: https://isitonrecall.com/recall/fda-device-z-1350-2023-easy-read-app-associated-with-first-response-pregnancy-test-sticks-intended-use-of-converting-analog/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Easy Read App associated with First Response Pregnancy Test Sticks - Intended use of converting analog pregnancy test... — FDA record Z-1350-2023

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 Jan 25, 2023. 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**: Easy Read App associated with First Response Pregnancy Test Sticks - Intended use of converting analog pregnancy test results into text pregnant or not pregnant for display on consumer devices (e.g., smart phone, iPad)
- **Reason**: Church & Dwight First Response Pregnancy Kits was marketed with the Easy Read App without a new 510k. There is also a potential for Easy Read App to be unable to reads the test results (i.e., no results reported on the APP screen) or to misread the analog results shown on the pregnancy test stick and may lead to misinterpretation of false positive or false negative tests by the user.
- **Classification**: Class II
- **Recalling firm**: Church & Dwight Inc
- **Quantity**: 780000 downloads
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1350-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1350-2023%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 | All lots with the Easy Read App |

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**: Apr 19, 2023
- **Recall initiation date**: Jan 25, 2023
- **Center classification date**: Apr 7, 2023

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-1350-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Church & Dwight Inc records](https://isitonrecall.com/brand/church-dwight-inc/)
