Health product recall

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

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

ALTIS SINGLE INCISION SLING SYSTEM

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

519650

Companies
Manufacturer

Coloplast A/S

Holtedam 1

Humlebaek

3050

DENMARK