FDA Device recall Z-2264-2020
PerkinElmer 226 Sample Collection Device
- FDA Device
- Class III
- terminated
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class III recall of PerkinElmer 226 Sample Collection Device by Perkinelmer Health Sciences, citing 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 wit….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2264-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-12-19 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Perkinelmer Health Sciences |
| Distribution | OH |
Product
PerkinElmer 226 Sample Collection Device
Reason
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.
Identifiers
| code_info | UDI: (01)50812589020011(17)200831(10)40020001; Serial Numbers: 06879601-06879700 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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All Perkinelmer Health Sciences recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2264-2020%22
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