oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

Furosemidum Polfarmex

The quality defect involves a mix-up of Furosemidum Polfarmex and Nasen packs, creating a risk that patients take the wrong medicine and consequently face a threat to their life or health. Potential effects: lack of efficacy, increased adverse effects, serious complications, life-threatening situations.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

Furosemidum Polfarmex
Risk Level
High
Manufacturer
Polfarmex S.A.
Batch Number
020320
EAN Code
05909990223794
Recall Date
15.06.2020
View official statement

Important Information

What You Should Know

Recommendations

Do not use Furosemidum Polfarmex or Nasen products from batch 020320. Check the batch number on the packaging and return the product to the pharmacy. If the wrong medicine has been taken, contact a do...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch 020320 of Furosemidum Polfarmex and Nasen from the market nationwide, granted the decision immediate enforceability, and obliged the marketing authori...

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 quality defect involves a mix-up of Furosemidum Polfarmex and Nasen packs, creating a risk that patients take the wrong medicine and consequently face a threat to their life or health. Potential effects: lack of efficacy, increased adverse effects, serious complications, life-threatening situations.
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: 020320

Related

Other Recalled Products