REMISOL ADVANCE (2021-07-15)

Starting date:

July 15, 2021

Posting date:

July 29, 2021

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-76101

Last updated: 2021-07-30

• Reason
• Affected products

Affected Products 

REMISOL ADVANCE

Reason

Beckman Coulter discovered an issue with the DiffPad feature of Remisol Advance versions 2.0 And 2.1. Whenever keyboard settings are configured to numerical values there is a chance that additional cell counts are added while performing a manual differential

Affected products