BD MAX assays (2019-07-19)

Starting date:

July 19, 2019

Posting date:

August 9, 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-70653

Last updated: 2019-08-09

• 
  Reason
• 
  Affected products

Affected Products

BD MAX assays

Reason

BD has discovered that approximately 1.4% of the foil bags containing Master Mix and extraction tubes for BD MAX Assays may not have been sealed properly.

Affected products