PerkinElmer 226 Sample Collection Device — Class III medical device recall Z-2264-2020
Terminated recall by PerkinElmer Health Sciences, Inc., reported 2020-06-10, distributed in OH. PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels th
| Recall number | Z-2264-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | PerkinElmer Health Sciences, Inc., Greenville, SC, United States |
| Recall initiated | 2017-12-19 |
| Classified | 2020-06-04 |
| Reported by FDA | 2020-06-10 |
| Terminated | 2021-03-26 |
| Distributed | OH |
| Quantity | 164,952 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 50812589020011 |
| Serial numbers | 06879601-06879700 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2264-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.