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Health product recall

Vanish (2017-09-22)

Starting date:
September 22, 2017
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
Healthcare Professionals, General Public, Hospitals
Identification number:
RA-64684

Affected products

Vanish

Reason

Affected lot was released to market without adequate testing.

Depth of distribution

Wholesalers and end-users (dental offices) in Ontario

Affected products

Vanish

DIN, NPN, DIN-HIM
NPN 80003435
Dosage form

Liquid

Strength

Sodium Fluoride 5.0%

Lot or serial number

N871667

Companies
Recalling Firm
3M Canada Company
300 Tartan Drive
London
N5V 4M9
Ontario
CANADA
Marketing Authorization Holder
3M Canada Company
300 Tartan Drive
London
N5V 4M9
Ontario
CANADA