PerkinElmer Health Sciences, Inc. recalls PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a mediu…
- Recall date
- May 31, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2756-2017
- FDA classification
- Class III
- Brand / firm
- PerkinElmer Health Sciences, Inc.
- Sold / distributed
- US Distribution to the state of : AL
Why it was recalled
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.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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.
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