FDA Device recall Z-2756-2017
PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and tra…
- FDA Device
- Class III
- terminated
- Published 2017-08-02
On 2017-08-02 the FDA classified a Class III recall of PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and tra… by Perkinelmer Health Sciences, citing 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 withi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2756-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-05-31 |
| Published | 2017-08-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Perkinelmer Health Sciences |
| Distribution | AL |
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
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.
Identifiers
| code_info | lot numbers 317113 and 317114 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Perkinelmer Health Sciences
- PerkinElmer 226 Sample Collection Device
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All Perkinelmer Health Sciences recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2756-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.