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Health product recall

Rave

Starting date:
June 20, 2013
Posting date:
July 17, 2013
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-34671

Recalled products

  1. Rave

Reason

This recall was initiated because this product is unauthorized and contains alkyle nitrate, which is considered a drug in Canada.

Depth of distribution

Retailers in Canada.

Affected products

A. Rave

DIN, NPN, DIN-HIM
Not applicable
Dosage form

Liquid

Strength

Not applicable

Lot or serial number

Not applicable

Companies
Recalling Firm
Kaytel Video Distribution Ltd.
2150 Ward Street,
Saint-Laurent
H4M 1T7
Quebec
CANADA
Marketing Authorization Holder
Not applicable

Date modified: