FDA Recall Terminated

SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product Usage: The SKINFUSE Rescue Calming Complex is intend to be used to soothe and calm skin (cosmetic). The SKINFUSE LIFT HG is a hydrogel wound dressing to protect against abrasion and friction during the microneedling procedure.

Recall: Z-0660-2020 · Initiated January 18, 2019

Recall

Recall Number
Z-0660-2020
Event Number
84154
Firm
Bellus Medical
FEI Number
3010392991
Product Code
QAI
Status
Terminated
Root Cause
Mixed-up of materials/components
Initiated
January 18, 2019
Terminated
March 5, 2021
Address
5005 LBJ Freeway, Ste 370, Dallas, TX, 75244-6144

Description

SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product Usage: The SKINFUSE Rescue Calming Complex is intend to be used to soothe and calm skin (cosmetic). The SKINFUSE LIFT HG is a hydrogel wound dressing to protect against abrasion and friction during the microneedling procedure.

Reason

Cosmetic Kit was packaged with a mislabel medical product.

Action

On 01/18/2019, the firm notified customers (medical practices) via a telephone and/or email informing them of an incorrect labeling of product and for the physicians to return the product and to dispose of any open products. Affected products contained the Lot Number 16053. In addition, the firm send an "URGENT: Notification to Practice" letter via certified mail to customer and included an "URGENT: Notification to Patients" template letter that physicians were to used to notify their patients of the recall action. Customer were instructed to complete and return an enclosed response form and if there were any questions to contact the Director of Quality & Regulatory at Office Number 888.372.3983 or Direct Number 972.232.2899.

Distribution

US Nationwide distribution.

Quantity

6007