PRISMAFLO IIS Blood Warmer (2019-02-28)

Starting date:

February 28, 2019

Posting date:

March 15, 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-69292

• 
  Reason
• 
  Affected products

Affected Products

PRISMAFLO IIS Blood Warmer

Reason

Stihler Electronic GMBH, the manufacturer of PRISMAFLO IIS blood warmers, has identified that damage to the heating profile of the PRISMAFLO blood warmers may result in a hotspot.

Affected products