# FDA recall Z-2264-2020

> **PerkinElmer Health Sciences, Inc.** · Class III · device recall initiated 2017-12-19.

## Product

PerkinElmer 226 Sample Collection Device

## Reason for recall

PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.

## Distribution

US  distribution in the state of Ohio

## Key facts

- **Recall number:** Z-2264-2020
- **Recalling firm:** PerkinElmer Health Sciences, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-19
- **Report date:** 2020-06-10
- **Termination date:** 2021-03-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Greenville, SC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2264-2020

## Citation

> AI Analytics. FDA recall Z-2264-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2264-2020. Source: US FDA. Licensed CC0.

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