# FDA recall Z-2620-2023

> **Copan Diagnostics Inc** · Class II · device recall initiated 2023-07-14.

## Product

COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs.

## Reason for recall

Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance

## Distribution

US: CA OUS: None

## Key facts

- **Recall number:** Z-2620-2023
- **Recalling firm:** Copan Diagnostics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-14
- **Report date:** 2023-09-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Murrieta, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2620-2023

## Citation

> AI Analytics. FDA recall Z-2620-2023. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-2620-2023. Source: US FDA. Licensed CC0.

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