PrecisionGlide Needle (2019-03-21)

Starting date:

March 21, 2019

Posting date:

April 5, 2019

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-69504

Last updated: 2019-04-05

• 
  Reason
• 
  Affected products

Affected Products

PrecisionGlide Needle

Reason

The unit label is printed with the incorrect catalog number and product description on the unit packaging only.

Affected products