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Health product recall

Pramipexole by Pro Doc Ltd. (2016-07-19)

Starting date:
July 19, 2016
Posting date:
July 27, 2016
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-59572

Affected products

Pramipexole

Reason

This lot of Pramipexole 1mg tablets may contain 0.5 mg tablets of Pramipexole.

Depth of distribution

Wholesalers and pharmacists in Québec

Affected products

Pramipexole

DIN, NPN, DIN-HIM
DIN 02325829
Dosage form

Tablet

Strength

1mg

Lot or serial number
  • 493270
Companies
Recalling Firm
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
Quebec
CANADA
Marketing Authorization Holder
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
Quebec
CANADA