Product Wiki · Recalls · Health Canada — Medical Devices

NUCLISENS LYSIS BUFFER (2017-07-13) — recall 57235

Health Canada — Medical Devices · Canada · 2017-10-30 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 57235
Date of alert: 2017-10-30
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Following a customer complaint related to coloured eluates for whole blood extractions when using NucliSENS Lysis Buffer ref 200292 - lot 17022802, an R&D investigation showed that the eluate becomes coloured because of the presence of the group heme.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/nuclisens-lysis-buffer-2017-07

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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.

NUCLISENS LYSIS BUFFER (2017-07-13) — recall 57235

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