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WARNING: RECALLED PRODUCT
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Dexapini

Sediment in the form of crystals was found at the bottom of the syrup bottle, not compliant with the quality specification. Failure to determine the cause of crystallization and the risk of disturbed antimicrobial protection and microbiological purity prevent ruling out a risk to patient health. Potential effects: infections, lack of treatment efficacy, health complications.

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Dexapini
Risk Level
High
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A. z siedzibą w Starogardzie Gdańskim
Batch Number
02092024
EAN Code
05909991031619
Recall Date
10.06.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use DEXAPINI syrup from the specified batches; check the batch number on the packaging and, if you have the product, return it to the pharmacy or place of purchase. If any concerning symptoms o...

Actions Taken

The DEXAPINI medicinal product batches 02092024 and 01122024 were withdrawn from the market throughout the country, placing these batches on the market was prohibited, and the decision was given immed...

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: Sediment in the form of crystals was found at the bottom of the syrup bottle, not compliant with the quality specification. Failure to determine the cause of crystallization and the risk of disturbed antimicrobial protection and microbiological purity prevent ruling out a risk to patient health. Potential effects: infections, lack of treatment efficacy, health 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: 02092024

Related

Other Recalled Products