oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

APHTIN

Non-compliant product odor and a decrease in active substance content were found, not meeting quality specifications. Potential effects: lack of treatment efficacy, possible adverse effects related to product degradation.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

APHTIN
Risk Level
Medium
Manufacturer
Laboratorium Galenowe Olsztyn Sp. z o.o.
Batch Number
00617, 00717, 00817, 00118, 00218, 00318, 00418, 00518
Recall Date
26.09.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the withdrawn batches, check the batch numbers; return any possessed packs to a pharmacy; in case of doubts or health problems, consult a doctor or pharmacist.

Actions Taken

Withdrawal from the market throughout the entire country of the specified medicinal product batches and granting 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: Non-compliant product odor and a decrease in active substance content were found, not meeting quality specifications. Potential effects: lack of treatment efficacy, possible adverse effects related to product degradation.
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: 00617, 00717, 00817, 00118, 00218, 00318, 00418, 00518

Related

Other Recalled Products