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

Verigene Processor SP, Model Numbers 10-0000-07 and 10-0000-07R. Used with assay Luminex, VERIGENE Gram-Negative Blood Culture Nucleic Acid Test, BC-GN, IVD - Product Usage: IVD sample processor, which utilizes a single-use disposable test consumable and a self-contained Verigene Test Cartridge for — recall Z-0477-2021

U.S. FDA — Device Enforcement · United States · 2020-10-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0477-2021
Date of alert
2020-10-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Luminex Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00857573006010
Reported risk: Luminex has determined that three (3) separate test fixtures used by field service engineers to service the VERIGENE SP Processors were procured from unapproved sources and, in some cases, were manufactured using unvalidated processes. These text fixtures were used to calibrate and verify VERIGENE SP devices.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.