Product Wiki · Recalls · Health Canada — Medical Devices

VYSIS SPECTRUM AQUA FISH PROBE KIT (2016-03-23) — recall 54747

Health Canada — Medical Devices · Canada · 2016-04-04 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
54747
Date of alert
2016-04-04
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: It has been recently identified that the Vysis LSI 9q34 SpectrumAqua FISH Probe Kit is no longer meeting Abbott Molecular's product quality specifications for specificity and background. As a result, non-specific fluorescent particles (aqua speckling) and/or background may interfere with signal interpretation.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/vysis-spectrum-aqua-fish-probe

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