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WARNING: RECALLED PRODUCT
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Paracetamol Aflofarm

Tests showed that despite shaking, sediment remains at the bottom of the bottle and some doses contain paracetamol outside the specification (e.g. 141.2 mg/5 ml with a limit of 114.0–126.0 mg/5 ml). Potential effects: risk of paracetamol overdose or incorrect treatment efficacy.

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Paracetamol Aflofarm
Risk Level
High
Manufacturer
Aflofarm Farmacja Polska sp. z o.o. z siedzibą w Pabianicach
Batch Number
wszystkie serie (m.in. 04AF0622, 01AF1122, 01AF1022, 02AF1022, 01AF0222, 03AF0622, 01AF0123)
EAN Code
05909991076115
Recall Date
10.07.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use Paracetamol Aflofarm 120 mg/5 ml oral suspension from any batch; check the medicine name on the pack and, if you have this product, return it to a pharmacy or consult a doctor or pharmacist...

Actions Taken

The Chief Pharmaceutical Inspector suspended the marketing of all batches of Paracetamol Aflofarm 120 mg/5 ml oral suspension throughout the country and granted the decision immediate enforceability; ...

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: Tests showed that despite shaking, sediment remains at the bottom of the bottle and some doses contain paracetamol outside the specification (e.g. 141.2 mg/5 ml with a limit of 114.0–126.0 mg/5 ml). Potential effects: risk of paracetamol overdose or incorrect treatment efficacy.
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: wszystkie serie (m.in. 04AF0622, 01AF1122, 01AF1022, 02AF1022, 01AF0222, 03AF0622, 01AF0123)

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