HistoCore PELORIS 3 (2018-05-16)

Starting date:

May 16, 2018

Posting date:

June 1, 2018

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-66926

• 
  Reason
• 
  Affected products

Affected products

HistoCore PELORIS 3

Reason

If operator initiates an operation in second retort or the protocol running concurrently in second retort causes a dialog box to appear when draining first retort at completion of protocol, a software defect may interrupt instrument workflow sequences in the first retort resulting in the impeller continuing to rotate.

Affected products