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WARNING: RECALLED PRODUCT
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Gripblocker Express

A quality defect was found: cracking of the soft gelatin capsule seam and leakage of the fill into the blister pocket, risking intake of an incomplete dose and lack of therapeutic effectiveness. Potential effects: lack of efficacy, persistence or worsening of symptoms.

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Gripblocker Express
Risk Level
Medium
Manufacturer
Przedsiębiorstwo Produkcji Farmaceutycznej Hasco-Lek S.A. z siedzibą we Wrocławiu
Batch Number
040623
EAN Code
05909991187392
Recall Date
14.08.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use capsules from batches 040623, 050623 and 060623; check the batch number on the packaging and, if you have the product, return it to a pharmacy; in case of doubts or lack of treatment effect...

Actions Taken

Batches 040623, 050623 and 060623 of GRIPBLOCKER EXPRESS were withdrawn from the market throughout the country and their placing on the market was prohibited; the decision was given immediate enforcea...

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 quality defect was found: cracking of the soft gelatin capsule seam and leakage of the fill into the blister pocket, risking intake of an incomplete dose and lack of therapeutic effectiveness. Potential effects: lack of efficacy, persistence or worsening of 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: 040623

Related

Other Recalled Products