FOLLTROPIN-V : affected lots may contain particulate matter
Brand(s)
Last updated
Summary
Product
FOLLTROPIN-V
Issue
Health products - Product quality
What to do
Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
Distribution
National
Affected products
| Brand | Product Name | Market Authorization | Dosage Form | Strength | Lot numbers |
|---|---|---|---|---|---|
| VETOQUINOL | FOLLTROPIN-V | DIN 00867357 | Powder For Solution | FOLLICLE STIMULATING HORMONE (FSH) 400 MG / VIAL | 510125, 510127, 510573, 510574, 713591 & 713592 |
Issue
The vial of sterile diluent in the affected lots may contain particulate matter.
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: Health Care Establishments
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
Vetoquinol N.-A. Inc.
2000 Chemin Georges
Lavaltrie, QC
J5T 3S5
Published by
Health Canada
Audience
General public
Healthcare
Industry
Distribution
National
Recall class
Type II
Recall date
Identification number
RA-78483
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