Impurity - Pro Doc MONTELUKAST SODIUM 5mg
Brand(s)
Last updated
Summary
Product
MONTELUKAST
Issue
Health products - Product quality
What to do
See instructions below.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot number |
|---|---|---|---|---|---|
MONTELUKAST |
Montelukast |
DIN 02379848 |
Tablet (Chewable) |
MONTELUKAST SODIUM 5mg |
637131 |
Issue
Presence of an unspecified impurity near the acceptable concentration limit in the affected lot.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
- Contact the recalling firm if you have any questions about the recall.
- Report any health product related side effects to Health Canada.
- Report any other health product safety complaints to Health Canada.
Additional information
Background
Depth of recall: Distributors and retailers
Details
Original published date: 2022-06-02
Alert / recall type
Health product recall
Category
Health product - Drugs
Companies
PRO DOC LIMITEE
2925 Boulevard Industriel
Laval, QC
H7L 3W9
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-64224