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

Recall Z-1268-2014 — AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum Quantitative determination of Uric Acid in serum.

U.S. FDA — Device Enforcement · United States · 2014-02-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1268-2014
Date of alert
2014-02-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
AMS Diagnostics, LLC
Product category
device
Product type
Devices
Reported risk: Marketing the devices outside 510(k) requirements
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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