Health CanadaType I
RIVA-Fluoxetine 10 mg capsule; may exceed the interim acceptable intake limit fo...
Published: July 3, 2025Recall ID: 77668Category: generalCountry: Canada
Reason for Recall / Hazard
Product quality
Product Description & Identification
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.
Affected Products
RIVA-Fluoxetine 10 mg capsule
Additional Source Details
| Field | Value |
|---|---|
| N I D | 77668 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/riva-fluoxetine-10-mg-capsule-may-exceed-interim-acceptable-intake-limit-n-nitroso |
| Issue | Product quality |
| Title | RIVA-Fluoxetine 10 mg capsule; may exceed the interim acceptable intake limit for N-nitroso-fluoxetine |
| Product | RIVA-Fluoxetine 10 mg capsule |
| Archived | 0 |
| Category | Drugs |
| Last updated | 2025-07-03 |
| Organization | Drugs and health products |
| Recall class | Type I |
| 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. |