VENLAFAXINE XR: out of specification
Brand(s)
Last updated
Summary
Product
VENLAFAXINE XR 75mg
Issue
Health products - Product quality
What to do
Consult your healthcare provider prior to discontinuing use of the affected product, or for any health concerns.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
VENLAFAXINE XR |
VENLAFAXINE XR |
DIN 02339250 |
Capsule (extended release) |
Venlafaxine (Venlafaxine Hydrochloride) 75mg |
2505003230 |
Issue
Dissolution is out of specification in the affected batch.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product, 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: Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
Pro-Doc Lté.
2925 boul. Industriel,
Laval, Qc,
H7L 3W9
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Recall date
Identification number
RA-81722
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