Thio med w/ dex, hem, vit k (10mL) (2018-08-13)

Starting date:

August 13, 2018

Posting date:

August 31, 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-67622

• 
  Reason
• 
  Affected products

Affected products

Thio med w/ dex, hem, vit k (10mL)

Reason

An internal technical investigation has confirmed that the above product, has intermittently failed performance testing during stability studies with various anaerobic microorganisms.

Affected products