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WARNING: RECALLED PRODUCT
PL EN

Aciclovir Jelfa

Due to the detected presence of particles visible to the naked eye, a risk to the patient’s health or life cannot be excluded. Potential effects: complications after intravenous administration, vessel damage, embolism, severe systemic reactions.

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Aciclovir Jelfa
Risk Level
Critical
Manufacturer
Bausch Health Ireland Limited, 3013 Lake Drive, Citywest Business Campus, Dublin 24, D24PPT3, Irlandia
Batch Number
111121
EAN Code
05909990405213
Recall Date
11.08.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 111121. Check the batch number of any held packs; if you have this batch, return the product to a pharmacy or wholesaler and consult a doctor about using an alternati...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch 111121 of Aciclovir Jelfa from the market throughout Poland and granted 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: Due to the detected presence of particles visible to the naked eye, a risk to the patient’s health or life cannot be excluded. Potential effects: complications after intravenous administration, vessel damage, embolism, severe systemic reactions.
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: 111121

Related

Other Recalled Products