Product Wiki · Recalls · Health Canada — Medical Devices

BD Veritor Plus Analyzer (2019-03-31) — recall 44546

Health Canada — Medical Devices · Canada · 2019-04-18 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
44546
Date of alert
2019-04-18
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: A limited number of BD Veritor Plus Analyzers are affected by an issue with their background calibration that has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor Plus Analyzer could lead to possible misdiagnosis and inappropriate treatment.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bd-veritor-plus-analyzer-2019-

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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