ALTIS SINGLE INCISION SLING SYSTEM (2021-01-22)

Starting date:

January 22, 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-74981

Last updated:
2021-02-12

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  Reason
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  Affected products

Affected Products 

ALTIS SINGLE INCISION SLING SYSTEM

Reason

This communication is to inform you that Coloplast has discontinued sales for the Altis Single Incision Sling system within the Canadian market. The decision and discontinuation action are not related to any product or safety concerns.

Affected products