MED-RX IV Kit (2018-12-17)

Starting date:

December 17, 2018

Posting date:

January 9, 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-68666

• 
  Reason
• 
  Affected products

Affected products

MED-RX IV Kit

Reason

Incorrect product in package. Product should have been packaged with Tegaderm 1683 (PN: BX1683) instead of Tegaderm 9525hp (PN:BX9525HP).

Affected products