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

Recall Z-0397-2017 — Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)

U.S. FDA — Device Enforcement · United States · 2016-10-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0397-2017
Date of alert
2016-10-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Healthcare Diagnostics, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10699201
Reported risk: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen Tubes- negative bias with plasma vs. serum samples
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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