Teva Octreotide for injectable suspension recalled due to potential drug quality issues
What the notice records
| Product | All strengths of Teva Octreotide for Injectable Suspension Kit (DIN 02503751, 02503778 and 0253786) with the lot numbers noted below. |
|---|---|
| Issue | Product quality |
| What you should do | If you have an affected product, do not use it. Speak to your health care professional immediately to obtain an alternative or replacement product. If you are unsure whether your product is affected, check with your pharmacy. Seek medical attention if you have used this product and are experiencing symptoms of infection, or other unexpected symptoms or side effects.Return affected product(s) to the pharmacy where it was purchased for proper disposal.Consult a health care professional if you have used the affected product and have health concerns.Contact Teva Canada Limited by calling toll-free at 1-800-268-4127, option 3, or by email at [email protected], if you have questions about this recall.Report any health product-related side effects or complaints to Health Canada. |
| Category | Drugs |
| Publishing body | Communications and Public Affairs Branch |
| Class | Class not stated |
| Last updated | 2026-01-13 |
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