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

Recall Z-2779-2016 — VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA technique (EnzymeLinked Fluo

U.S. FDA — Device Enforcement · France · 2016-04-15 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2779-2016
Date of alert: 2016-04-15
Country / jurisdiction: France
Risk level: Class III
Risk type: recall
Brand: Biomerieux France Chemin De L'Or
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 1004474560

Reported risk: Due to a packaging error; The kit does not contain the correct number of C1 or C2 control vials.

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.

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.

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