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

Recall Z-0827-2015 — Glucose Hexokinase (Liquid) Reagent For the in vitro quantitative determination of Glucose in serum.

U.S. FDA — Device Enforcement · United States · 2014-10-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0827-2015
Date of alert
2014-10-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
JAS Diagnostics Inc.
Product category
device
Product type
Devices
Reported risk: Product is not performing according to specifications. Control 2 does not consistently recover within its assigned range.
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.

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