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

Recall Z-2124-2015 — Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wizard¿" gamma counter is intended to detect and count gamma radiation emitted by clinical samples.

U.S. FDA — Device Enforcement · United States · 2015-06-03 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2124-2015
Date of alert
2015-06-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Perkinelmer
Product category
device
Product type
Devices
Reported risk: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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.

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.