---
title: "COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 100... — FDA record Z-2620-2023 | Is It on Recall"
description: "Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance"
url: https://isitonrecall.com/recall/fda-device-z-2620-2023-copan-ref-2u045s01-300ul-transfer-pipette-individually-wrapped-pipettes-1000-pcs/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs. — FDA record Z-2620-2023

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 Jul 14, 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**: COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs.
- **Reason**: Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance
- **Classification**: Class II
- **Recalling firm**: Copan Diagnostics Inc
- **Quantity**: 2,592 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2620-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2620-2023%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 | UDI-50841467100545 / Lot Codes: B104661 B202918 B203404 B203405 B204186 B204187 B204819 B204820 B300133 B300410 B300608 B300647 B300679 B301129 B301133 B301135 B301134 |

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

## Distribution

US: CA OUS: None

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/)

## Dates in the source

- **Report date**: Sep 27, 2023
- **Recall initiation date**: Jul 14, 2023
- **Center classification date**: Sep 20, 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-2620-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Copan Diagnostics Inc records](https://isitonrecall.com/brand/copan-diagnostics-inc/)