Product Wiki · Recalls · Health Canada — Medical Devices

BD Vacutainer Sodium Fluoride Tube (2019-06-14) — recall 59761

Health Canada — Medical Devices · Canada · 2019-08-30 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
59761
Date of alert
2019-08-30
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: BD is conducting a voluntary medical device recall for a lot of BD Vacutainer Fluoride Tubes for Blood Alcohol Determinations. A small portion of this lot has been confirmed to have no additive within tube.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bd-vacutainer-sodium-fluoride-

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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