Health product recall

Aldara P (2020-07-13)

Starting date:
July 13, 2020
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-73579

Last updated: 2020-07-20

Summary

  • Product: Aldara P

Reason

The pump delivery by weight is out of specification in the affected lot.

Depth of distribution

Retailers

Affected products

Aldara P

DIN, NPN, DIN-HIM

DIN 02239505

Dosage form

Cream

Strength

Imiquimod 5%

Lot or serial number

7000450

Companies

Recalling Firm
Bausch Health Canada Inc
2150 Boulevard St-Elzéar
Laval
H7L 4A8
Quebec
CANADA
Marketing Authorization Holder
Bausch Health Canada Inc
2150 Boulevard St-Elzéar
Laval
H7L 4A8
Quebec
CANADA