Product Wiki · Recalls · Health Canada — Medical Devices

CLINITEK NOVUS 10 AND PRO 10 URINALYSIS CASSETTES (2015-12-21) — recall 54238

Health Canada — Medical Devices · Canada · 2016-01-14 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
54238
Date of alert
2016-01-14
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: Siemens Healthcare Diagnostics has confirmed that certain lots of CLINITEK Novus Urinalysis cassettes may report glucose as "error" for some urine samples and negative quality controls more frequently than expected.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/clinitek-novus-10-and-pro-10-u

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