---
title: "Kreatech PapV-16, Flu labeled ISH probe, to detect presence of HPV-16 DNA ins... — FDA record Z-0522-2025 | Is It on Recall"
description: "The DNA fragments for this specific lot number are too large, resulting in potential background around the cells due to suboptimal hybridization. An absence of"
url: https://isitonrecall.com/recall/fda-device-z-0522-2025-kreatech-papv-16-flu-labeled-ish-probe-to-detect-presence-of-hpv-16-dna-inserts-in-human-tissue-mode/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Kreatech PapV-16, Flu labeled ISH probe, to detect presence of HPV-16 DNA inserts in human tissue, Model Number 40V01... — FDA record Z-0522-2025

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 Nov 1, 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**: Kreatech PapV-16, Flu labeled ISH probe, to detect presence of HPV-16 DNA inserts in human tissue, Model Number 40V016V495
- **Reason**: The DNA fragments for this specific lot number are too large, resulting in potential background around the cells due to suboptimal hybridization. An absence of signal could also be observed as a result of the suboptimal hybridization of the larger DNA fragments. The user may interpret potential background as a false positive result and an absence of signal as a false negative result, if proper positive and negative controls are not included.
- **Classification**: Class II
- **Recalling firm**: Kreatech Biotechnology Bv
- **Quantity**: 23 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0522-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0522-2025%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: (01)08718858480241 Lot Number: 00088454 |

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

## Distribution

US States: FL, NY

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

- [Florida](https://isitonrecall.com/state/florida/)
- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Dec 4, 2024
- **Recall initiation date**: Nov 1, 2024
- **Center classification date**: Nov 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-0522-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Kreatech Biotechnology Bv records](https://isitonrecall.com/brand/kreatech-biotechnology-bv/)