PRO-Fluoxetine 10 mg capsule; may exceed the interim acceptable intake limit for N-nitroso-fluoxetine
Brand(s)
Last updated
Summary
Product
PRO-Fluoxetine 10 mg capsule
Issue
Health products - Product quality
What to do
Consult your health care professional if you have any health concerns.
Affected products
| Brand | Product Name | Market Authorization | Dosage Form | Strength | Lot number |
|---|---|---|---|---|---|
| Pro Doc Limitée | PRO-Fluoxetine 10 mg capsule | DIN 02314991 | Capsule | Fluoxetine hydrochloride 10 mg | 651194, 656543, 658509, 659876 |
Issue
Affected lots may exceed the interim acceptable intake limit for N-nitroso-fluoxetine.
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.
Related recalls and alerts
Additional information
Background
Depth of recall: Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
Pro Doc Limitée
2925 Boulevard Industriel
Laval Quebec H7L 3W9 Canada
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type I
Identification number
RA-77659
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