What does this decision mean?
An exceedance of the quality specification limit for the parameter "each single impurity" was found in batch No. 02AF1024. The authority states that a risk to human health from keeping this batch on the market, when used in children, cannot be excluded. Potential effects: possible toxic effects or reduced treatment safety.
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A recall means the product may be unsafe. Here is what to do if you have it at home.
Do not eat or use the product
Stop using or consuming it immediately and keep it out of reach of children.
Check the batch number and expiry date
Compare the batch/lot number and the best-before or expiry date with the details in the alert — sometimes only specific batches are affected.
Return it to the shop
You can take the product back to the shop where you bought it. For a safety recall a refund is due even without a receipt.
Get help and report it
If you feel unwell after using the product, contact a doctor. You can also report the case to the relevant authority — GIS, GIF or UOKiK.
General guidance for recalled products in Poland. Always follow the specific instructions in the official alert and from the manufacturer or retailer.
Important Information
• Do not use Kidofen (Ibuprofen), 125 mg, suppositories from batch No. 02AF1024. • Check the batch number on the package; if you have batch 02AF1024, return the product to a pharmacy. • If in doubt or...
• The Chief Pharmaceutical Inspector recalled from the entire Polish market the medicinal product Kidofen (Ibuprofen), 125 mg, suppositories, pack of 10, GTIN 05909990948895, for batch No. 02AF1024. •...
If you feel unwell after consuming this product, contact your doctor or call the poison control center.
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