Product Wiki · Recalls · Health Canada — Medical Devices

BD PrecisionGlideTM Needle 19GX1-1/2IN (2020-01-14) — recall 63152

Health Canada — Medical Devices · Canada · 2020-02-14 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
63152
Date of alert
2020-02-14
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: This is a non-health/non-safety related risk. The reported current event/issue does not have the potential to cause harm directly and/or indirectly to patients or users or anyone else that comes in contact with the product. In addition, the current event/issue has not led to the identification of a new harm, an increase in the severity of harm, or the occurrence rate of harm, of a previously identified adverse health effect.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bd-precisionglidetm-needle-19g

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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.