oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

Linezolid Polpharma

Stability testing showed non-compliance in active substance release after 30 minutes, which may affect the product’s effectiveness and poses a real risk to patient health due to potential lack of efficacy. Potential effects: treatment failure, risk of infection progression.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

Linezolid Polpharma
Risk Level
Medium
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A. z siedzibą w Starogardzie Gdańskim
Batch Number
10421
EAN Code
05909991242718
Recall Date
17.11.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batches 10421 and 10421A, check the batch numbers on the packaging and return the product to the pharmacy; if there are concerns about the effectiveness of past treatment, ...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batches 10421 and 10421A of Linezolid Polpharma 600 mg from the national market, prohibited their placing on the market, and granted the decision immediate ...

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: Stability testing showed non-compliance in active substance release after 30 minutes, which may affect the product’s effectiveness and poses a real risk to patient health due to potential lack of efficacy. Potential effects: treatment failure, risk of infection progression.
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: 10421

Related

Other Recalled Products