---
title: "1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum tr... — FDA record Z-0942-2026 | Is It on Recall"
description: "Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed."
url: https://isitonrecall.com/recall/fda-device-z-0942-2026-1ml-of-dtt-in-liquid-phase-in-pet-tube-with-capture-cap-in-bulk-sputum-transfer-device-for-wasp-comp/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP\* \*Compatible wit... — FDA record Z-0942-2026

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 Oct 29, 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**: 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP\* \*Compatible with Copan s WASP (Walk-Away Specimen Processor for Microbiology) System
- **Reason**: Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
- **Classification**: Class II
- **Recalling firm**: Copan Italia
- **Quantity**: 122,850 units US
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0942-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0942-2026%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 | UDI:0U020N.A - (01)18053326005036 |

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

## Distribution

US Distribution to states of: CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT

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

- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)

## Dates in the source

- **Report date**: Dec 24, 2025
- **Recall initiation date**: Oct 29, 2025
- **Center classification date**: Dec 18, 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-0942-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Copan Italia records](https://isitonrecall.com/brand/copan-italia/)