FDA Device recall Z-0030-2014
Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900
- FDA Device
- Class II
- terminated
- Published 2013-10-30
On 2013-10-30 the FDA classified a Class II recall of Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900 by Perkin Elmer Health Sciences, citing some devices may be contaminated on the back side of the device with glue in the blood application area.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0030-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-05 |
| Published | 2013-10-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Perkin Elmer Health Sciences |
| Distribution | OH |
Product
Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the collection of demographic information.
Reason
Some devices may be contaminated on the back side of the device with glue in the blood application area.
Identifiers
| code_info | Job number: 313119, Item Lot number: Ohio HEA 2518, Serial numbers: 06132903 - 06198900. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0030-2014%22
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