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

Recall Z-1327-2020 — OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565

U.S. FDA — Device Enforcement · United Kingdom · 2019-07-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1327-2020
Date of alert
2019-07-29
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)
05051700017565
Reported risk: There is a potential that users may experience difficulty validating the calibration of the kit. This is indicated by kit control values reporting outside the specified ranges. This could result in potential false patient results which could cause a delay until repeat testing is performed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.