---
title: "Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing L... — FDA record Z-0138-2025 | Is It on Recall"
description: "The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the validated summer packaging and may have been exposed to temperatures above 25¿C. Thi"
url: https://isitonrecall.com/recall/fda-device-z-0138-2025-quantimetrix-urine-chemistry-control-set-dipper-urinalysis-dipstick-testing-levels-1-2-6-x-15-ml-ivd/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing Levels 1 & 2 6 X 15 mL-IVD intended as a ... — FDA record Z-0138-2025

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 17, 2024. 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**: Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing Levels 1 & 2 6 X 15 mL-IVD intended as a control for urinalysis reagent strips, microalbumin, and creatinine by listed test methods.
- **Reason**: The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the validated summer packaging and may have been exposed to temperatures above 25¿C. This may lead to delay in patients' results.
- **Classification**: Class II
- **Recalling firm**: Mckesson Medical-Surgical Inc. Corporate Office
- **Quantity**: 1 BOX
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0138-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0138-2025%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 | UDI-DI: 896863002134 |

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

## Distribution

US Nationwide distribution in the state of DC.

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**: Oct 30, 2024
- **Recall initiation date**: Sep 17, 2024
- **Center classification date**: Oct 22, 2024

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-0138-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mckesson Medical-Surgical Inc. Corporate Office records](https://isitonrecall.com/brand/mckesson-medical-surgical-inc-corporate-office/)
