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WARNING: RECALLED PRODUCT
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APAP Intense

It was found that the medicinal product sample does not meet the specification in the product documentation regarding the appearance parameter, which constitutes a quality defect. Potential effects: possible reduced treatment efficacy or unpredictable drug action.

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APAP Intense
Risk Level
Medium
Manufacturer
US Pharmacia Sp. z o.o. z siedzibą we Wrocławiu
Batch Number
P2009118
EAN Code
05909991430924
Recall Date
17.03.2022
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch P2009118; patients should check the batch number, return the package to the pharmacy, and consult a doctor or pharmacist if in doubt.

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch P2009118 of APAP Intense from the entire country, granted the decision immediate enforceability, and obliged the marketing authorisation holder to car...

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: It was found that the medicinal product sample does not meet the specification in the product documentation regarding the appearance parameter, which constitutes a quality defect. Potential effects: possible reduced treatment efficacy or unpredictable drug action.
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: P2009118

Related

Other Recalled Products