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WARNING: RECALLED PRODUCT
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Gripblocker Express

The quality defect consists of cracking of the soft gelatin capsule seams and leakage of the filling into the blister pocket, creating a real risk to patients’ health due to the possibility of receiving an incomplete dose and lack of treatment effectiveness. Potential effects: lack of treatment efficacy, possible complications of the underlying disease.

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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 capsules from the listed batches. Check the batch number on the packaging and return any affected packs to the pharmacy or consult a pharmacist or doctor about further steps.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of the product from the market throughout the country, prohibited their placing on the market, and granted the decision immediate enfo...

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 quality defect consists of cracking of the soft gelatin capsule seams and leakage of the filling into the blister pocket, creating a real risk to patients’ health due to the possibility of receiving an incomplete dose and lack of treatment effectiveness. Potential effects: lack of treatment efficacy, possible complications of the underlying disease.
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