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WARNING: RECALLED PRODUCT
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Gripblocker Express

Cracking of the soft gelatin shell seams and leakage of the capsule fill into the blister pocket were found, creating a real risk to patients’ health through the possibility of taking an incomplete dose and lack of effectiveness of the medicinal product. Potencjalne skutki: lack of treatment effectiveness, worsening or prolongation of disease symptoms.

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Gripblocker Express
Risk Level
Medium
Manufacturer
Przedsiębiorstwo Produkcji Farmaceutycznej Hasco-Lek S.A. z siedzibą we Wrocławiu
Batch Number
010623
EAN Code
05909991187392
Recall Date
29.08.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batches 010623, 020623 and 030623. Check the batch number on the packaging; if you have a product from these batches, return it to the pharmacy or place of purchase. If you...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batches 010623, 020623 and 030623 of GRIPBLOCKER EXPRESS from the market throughout the country, prohibited placing these batches on the market, and granted...

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: Cracking of the soft gelatin shell seams and leakage of the capsule fill into the blister pocket were found, creating a real risk to patients’ health through the possibility of taking an incomplete dose and lack of effectiveness of the medicinal product. Potencjalne skutki: lack of treatment effectiveness, worsening or prolongation of disease symptoms.
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: 010623

Related

Other Recalled Products