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WARNING: RECALLED PRODUCT
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Risperidone Teva

Testing by the National Medicines Institute (OMCL) showed an out-of-specification result for the release parameter at a defined time point and temperature, meaning the product does not meet quality requirements and concerns a critical parameter affecting the drug’s action. Potential effects: lack of therapeutic efficacy or its disturbance, possible clinical complications.

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Risperidone Teva
Risk Level
Critical
Manufacturer
Teva B.V. z siedzibą w Haarlem, Holandia
Batch Number
wszystkie serie (badana seria: 4201479)
EAN Code
05909991457921
Recall Date
30.12.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the suspended batches. Patients should contact their physician to determine further treatment and any therapy change. Pharmacies and healthcare institutions should not disp...

Actions Taken

The marketing of the medicinal product RISPERIDONE TEVA 37.5 mg for all batches was suspended throughout the country, and the decision was given immediate enforceability after a negative quality test ...

Need Help?

If you feel unwell after consuming this product, contact your doctor or call the poison control center.

FAQ

Frequently Asked Questions

Is this product safe to consume?
No. This product has been recalled due to: Testing by the National Medicines Institute (OMCL) showed an out-of-specification result for the release parameter at a defined time point and temperature, meaning the product does not meet quality requirements and concerns a critical parameter affecting the drug’s action. Potential effects: lack of therapeutic efficacy or its disturbance, possible clinical complications.
What should I do if I already bought this?
Stop using the product immediately. Return it to the store for a full refund. If you consumed it and feel unwell, contact your doctor.
Which batches are affected?
Affected batch numbers: wszystkie serie (badana seria: 4201479)

Related

Other Recalled Products