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

Recall Z-1179-2014 — Cannabinoids DAU Calibrator Control Level 1 (62.5 ng/mL) This solution is prepared from non-sterile urine and should be handled as potentially infectious. IVD; The Cannabinoids (cTHC also known as THC version c) DAU negative and positive controls are human urine-based liquids and ready to use

U.S. FDA — Device Enforcement · United States · 2014-02-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1179-2014
Date of alert
2014-02-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Lin-Zhi International Inc
Product category
device
Product type
Devices
Reported risk: Product catalog #s 0007c Cannabinoid 37.5 ng/mL Control Level 1 and 0008c Cannabinoid 62.5 Control Level 2 of the lots mentioned may give decreased concentration readings towards the end of their shelf life due to use of dated but unexpired secondary stock used to create the products.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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