Straumann Jason Membrane (2021-02-04)

Starting date:

February 4, 2021

Posting date:

February 12, 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-74991

Last updated: 2021-02-12

• Reason
• Affected products

Affected Products 

Straumann Jason Membrane

Reason

The listed batches of Jason Membrane distributed to and in Canada, were subjected to a raw material supplier change which has not been sufficiently evaluated. The supplier has introduced a change on the animal tissue sourcing without appropriate notification. After becoming aware of this change, it was determined that it had been implemented without the appropriate amendment notification to Health Canada License No. 101739

Affected products