Product Wiki · Recalls · U.S. FDA — Device Enforcement

PerkinElmer 226 Sample Collection Device — recall Z-2264-2020

U.S. FDA — Device Enforcement · United States · 2017-12-19 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2264-2020
Date of alert
2017-12-19
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
PerkinElmer Health Sciences, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50812589020011
Reported risk: 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.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.