StrykeProbe Tips (2019-09-26)

Starting date:

September 26, 2019

Posting date:

October 11, 2019

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-71269

Last updated: 2019-10-11

• 
  Reason
• 
  Affected products

Affected Products

StrykeProbe Tips

Reason

Manufacturer became aware that the sheath tube had a sheath hub that was not fully seated on the sheath tube. The sheath being too long poses a potential risk for the distal tip of the sheath to melt.

Affected products