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

Recall Z-2407-2020 — Utak NR Trace Elements Serum Control, 5 ml, REF 66816. The responsible firm on the label is UTAK LABORATORIES, INC., Valencia, CA. Control for in vitro diagnostics.

U.S. FDA — Device Enforcement · United States · 2020-03-20 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2407-2020
Date of alert
2020-03-20
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Utak Laboratories Inc
Product category
device
Product type
Devices
Reported risk: The product has an incorrect reference value for cadmium and an incorrect expected 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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