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WARNING: RECALLED PRODUCT
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Ibuprofen Dr. Max

A justified suspicion of non-compliance with quality requirements concerned the loss on drying parameter for batch DQ2011, which could indicate deviations in capsule quality, but subsequent analyses showed compliance with the extended specification. Potential effects: no significant health effects for patients.

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Ibuprofen Dr. Max
Risk Level
Low
Manufacturer
Dr. Max Pharma s.r.o. z siedzibą w Pradze
Batch Number
wszystkie serie, w tym badana seria DQ2011
EAN Code
08595566451783
Recall Date
01.08.2025
View official statement

Important Information

What You Should Know

Recommendations

The product may be used according to the package leaflet; in case of any doubts, patients should consult a doctor or pharmacist.

Actions Taken

The Chief Pharmaceutical Inspectorate declared the expiry of decision No. 6/WS/2024 suspending the distribution of Ibuprofen Dr. Max 400 mg soft capsules nationwide, recognizing that all batches do no...

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: A justified suspicion of non-compliance with quality requirements concerned the loss on drying parameter for batch DQ2011, which could indicate deviations in capsule quality, but subsequent analyses showed compliance with the extended specification. Potential effects: no significant health effects for patients.
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, w tym badana seria DQ2011

Related

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