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

Starting date:

January 14, 2020

Posting date:

February 14, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-72315

Last updated: 2020-02-14

• Reason
• Affected products

Affected Products

BD PrecisionGlideTM Needle 19GX1-1/2IN

Reason

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.

Affected products