oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

Triderm

The occurrence of incorrect information on the outer packaging regarding the repackaging site and the name of the parallel importer was classified as a quality defect of the medicinal product. Potential effects: incorrect use of the drug, inability to identify the responsible entity, possible therapy complications.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

Triderm
Risk Level
High
Manufacturer
Podmiot uprawniony do importu równoległego: PharmaVitae Sp. z o.o. Sp. k. z siedzibą w Leśnej
Batch Number
T016521
EAN Code
5909991391249
Recall Date
29.10.2020
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from this batch, check the batch number on the packaging and, if it matches, return the product to the pharmacy or consult a pharmacist or doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the indicated batch of the medicinal product from the market throughout the country and granted the decision immediate enforceability; the responsible entit...

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 occurrence of incorrect information on the outer packaging regarding the repackaging site and the name of the parallel importer was classified as a quality defect of the medicinal product. Potential effects: incorrect use of the drug, inability to identify the responsible entity, possible therapy complications.
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: T016521

Related

Other Recalled Products