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
Get notified
Receive emails about new and updated recall and safety alerts.