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WARNING: RECALLED PRODUCT
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Duracef

Testing showed a lower value of cefadroxil release within 30 minutes, so a risk to patient health due to lack of drug efficacy cannot be excluded. Potential effects: lack of treatment effectiveness, possible disease complications.

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Duracef
Risk Level
Medium
Manufacturer
Bausch Health Ireland Limited, Irlandia
Batch Number
2209025
EAN Code
05909990050826
Recall Date
14.06.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use DURACEF from batch 2209025; if you have this product, return it to a pharmacy and, if you have any concerns regarding treatment, contact your doctor.

Actions Taken

Withdrawal of DURACEF batch 2209025 from the market throughout the country 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: Testing showed a lower value of cefadroxil release within 30 minutes, so a risk to patient health due to lack of drug efficacy cannot be excluded. Potential effects: lack of treatment effectiveness, possible disease 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: 2209025

Related

Other Recalled Products