Shigella Sonnei (Phases 1 and 2) Agglutinating Serum (2017-11-21)

Starting date:

November 21, 2017

Posting date:

January 8, 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-65528

• Reason
• Affected products

Affected Products

Shigella Sonnei (Phases 1 and 2) Agglutinating Serum

Reason

An internal technical investigation has determined that Shigella Sonnei (Phases 1 and 2) Agglutinating Serum (lots listed) may fail to agglutinate within the specified minimum reaction time when tested with Shigella Sonnei Phase 2 bacteria.

Affected products