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

Recall Z-1184-2018 — Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator is an in vitro diagnostic product for the calibration of follicle stimulating hormone (FSH), luteinizing hormone (LH), prolactin (PRL), and estradiol (E2) methods on the Dimension Vista System.

U.S. FDA — Device Enforcement · United States · 2017-11-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1184-2018
Date of alert
2017-11-09
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)
00842768026492
Reported risk: An increase in the number of failed calibration events or negative bias with Quality Control (QC) and patient samples when using Dimension Vista LOCI 8 Calibrator lot 7CD076 to calibrate Estradiol (E2) Assay.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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