# FDA recall Z-2756-2017

> **PerkinElmer Health Sciences, Inc.** · Class III · device recall initiated 2017-05-31.

## Product

PerkinElmer 226 Sample Collection Device    The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory in Newborn Screening.

## Reason for recall

PerkinElmer 226 Sample Collection Devices Lot Number 317114 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 to the state of : AL

## Key facts

- **Recall number:** Z-2756-2017
- **Recalling firm:** PerkinElmer Health Sciences, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-31
- **Report date:** 2017-08-02
- **Termination date:** 2017-07-27

- **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-2756-2017

## Citation

> AI Analytics. FDA recall Z-2756-2017. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2756-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*