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WARNING: RECALLED PRODUCT
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Accupro 40

The letter concerned a request for a decision to withdraw the specified batches of medicinal products from the market due to the presence of contamination (N-nitroso-quinapril) above the permitted daily intake limit. Potential effects: possible carcinogenic effects, organ damage, complications of hypertension therapy.

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Accupro 40
Risk Level
Critical
Manufacturer
Pfizer Europe MA EEIG z siedzibą w Belgii
Batch Number
FN6679
EAN Code
05909991080129
Recall Date
25.04.2022
View official statement

Important Information

What You Should Know

Recommendations

Do not use the listed batches of ACCUPRO. Patients should check the batch number on their pack and, if it matches, return the product to the pharmacy and consult their doctor about further treatment.

Actions Taken

Withdrawal of the specified batches of ACCUPRO medicinal products from the market throughout Poland and granting the decision immediate enforceability; the marketing authorisation holder is obliged to...

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 letter concerned a request for a decision to withdraw the specified batches of medicinal products from the market due to the presence of contamination (N-nitroso-quinapril) above the permitted daily intake limit. Potential effects: possible carcinogenic effects, organ damage, complications of hypertension therapy.
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: FN6679

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