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WARNING: RECALLED PRODUCT
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Accupro 20

the presence of the impurity (N-nitroso-quinapril) above the acceptable daily intake limit. Potential effects: increased risk of toxicity and carcinogenic effects, especially during long-term use.

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Accupro 20
Risk Level
Medium
Manufacturer
Pfizer Europe MA EEIG z siedzibą w Belgii
Batch Number
FM6645
EAN Code
05909990707119
Recall Date
25.04.2022
Category
Medicines & supplements
View official statement

Important Information

What You Should Know

Recommendations

Do not use products from the listed batches, check the batch number on the packaging, and if you have the medicine, consult a doctor or pharmacist and return the packs to a pharmacy.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of ACCUPRO from the market throughout the country and granted the decision immediate enforceability, obliging the marketing authorisat...

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: the presence of the impurity (N-nitroso-quinapril) above the acceptable daily intake limit. Potential effects: increased risk of toxicity and carcinogenic effects, especially during long-term use.
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: FM6645

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