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WARNING: RECALLED PRODUCT
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Mupina

detection during stability studies of out-of-specification results regarding an unknown impurity… it cannot be ruled out that keeping this product on the market may pose a risk to patient health. Potential effects: unknown adverse reactions, possible risk to patients’ health.

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Mupina
Risk Level
High
Manufacturer
INFECTOPHARM Arzneimittel und Consilium GmbH, Niemcy
Batch Number
101912.1
EAN Code
05909991404321
Recall Date
06.10.2022
View official statement

Important Information

What You Should Know

Recommendations

Do not use ointment from the listed batches; check the batch number on the packaging and, if you have the product, return it to the pharmacy; if any worrying symptoms occur after use, contact a doctor...

Actions Taken

Withdrawal from the market throughout the country of batches 101912.1, 101913.1 and 102111.1 of Mupina nasal ointment 20 mg/g 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: detection during stability studies of out-of-specification results regarding an unknown impurity… it cannot be ruled out that keeping this product on the market may pose a risk to patient health. Potential effects: unknown adverse reactions, possible risk to patients’ health.
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: 101912.1

Related

Other Recalled Products