---
title: "healthmark ProChek-II, Model Number PT-313, PT-201-12 — FDA record Z-3031-2026 | Is It on Recall"
description: "Test manufactured with an expired ingredient which may present as either a false negative or positive."
url: https://isitonrecall.com/recall/fda-device-z-3031-2026-healthmark-prochek-ii-model-number-pt-313-pt-201-12/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# healthmark ProChek-II, Model Number PT-313, PT-201-12 — FDA record Z-3031-2026

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 Jul 29, 2026. 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**: healthmark ProChek-II, Model Number PT-313, PT-201-12
- **Reason**: Test manufactured with an expired ingredient which may present as either a false negative or positive.
- **Classification**: Class II
- **Recalling firm**: Healthmark Industries Co., Inc.
- **Quantity**: 5090 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3031-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3031-2026%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 | PT-313 - Serial/Lot Numbers: 3000535312, 3000535333, 3000536416, 3000536423, 3000537810, 3000537822, 3000542453, 3000545623, 3000550099, 3000550512, 313069, 313072, 313073, 313074, 313075, 313076, 313077, 313078, 313079, 313080, 313081, 313082, 313083, 313084, 313085, 313086, 313087, 313088, 313089, 313090, 313091, 313092, 313093, 313094, 313095, 313096, 313097, 313098, 313099, 313100, 313101, 313102, 313106, 313107; H-PT-201-12 - Serial/Lot Numbers: 7P0110, 7P0111, 7P0113, 7P0122. |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, France, Hong Kong, South Korea.

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

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## Dates in the source

- **Report date**: Sep 2, 2026
- **Recall initiation date**: Jul 29, 2026
- **Center classification date**: Aug 26, 2026

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-3031-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Healthmark Industries Co., Inc. records](https://isitonrecall.com/brand/healthmark-industries-co-inc/)
