Reliance Blunt Probe (2018-11-19)

Starting date:

November 19, 2018

Posting date:

December 10, 2018

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-68544

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  Reason
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  Affected products

Affected products

Reliance Blunt Probe

Reason

During a Quality Control inspection of the spherical diameter on the Reliance Blunt Probe, it was detected that parts were not conforming. Specifically, instead of having a spherical diameter, the probe was observed to have 2 radii and a flat surface. Additionally, it was observed that some parts exhibited an edge on the intersection between the radius and the diameter of the probe.

Affected products