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

Recall Z-1018-2017 — Optilite Analyser, Product Code: IE700 Product Usage: The Thermo Scientific Indiko Clinical Chemistry Analyzer is a fully automated random access analyzer used to measure a variety of analytes that may be adaptable to the analyzer depending on the reagent used. The Indiko Glucose (H-K) test syst

U.S. FDA — Device Enforcement · United Kingdom · 2015-05-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1018-2017
Date of alert: 2015-05-13
Country / jurisdiction: United Kingdom
Risk level: Class II
Risk type: recall
Brand: The Binding Site Group, Ltd.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 864000290243

Reported risk: Potential risk of the Optilite lid/cover falling suddenly and causing injury when not placed in the fully open position.

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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