Product Wiki · Recalls · Health Canada — Medical Devices

VACUETTE 4 ML FX SODIUM FLUORIDE / POTASSIUM OXAL (2016-04-26) — recall 55260

Health Canada — Medical Devices · Canada · 2016-05-31 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
55260
Date of alert
2016-05-31
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: The 4 mL FX Sodium Fluoride/Potassium Oxalate tube may have no or low additive (Sodium Fluoride and Potassium Oxalate), which can effect analytical results for glucose and lactate.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/vacuette-4-ml-fx-sodium-fluori

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