FDAFDA · Food and drugs·Recall number Z-2264-2020
PerkinElmer 226 Sample Collection Device
Published June 10, 2020 · Recall initiated: December 19, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- PerkinElmer Health Sciences, Inc.
- Distributor
- US distribution in the state of Ohio
- Lot
- UDI: (01)50812589020011(17)200831(10)40020001; Serial Numbers: 06879601-06879700
- Risk classification
- Class III
- Area (FDA)
- device
- Country
- United States
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