Product Wiki · Recalls · Health Canada — Medical Devices

DRUGCHECK DRUG SCREEN CUP (2016-03-30) — recall 55259

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

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Agency
Health Canada — Medical Devices
Recall identifier
55259
Date of alert
2016-05-31
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: Affected lots of EDIs drugs of abuse tests have shown reduced reactivity for up to three (3) of the nineteen (19) benzodiazepine compounds for which specificity information is provided in the product insert. Specific compounds for which there may be reduced reactivity include clonazepam, nordiazepam and lorazepam. The test continues to perform as expected for other drugs.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/drugcheck-drug-screen-cup-2016

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