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WARNING: RECALLED PRODUCT
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Diprophos

A possible occurrence of brown particles with a metallic appearance, identified as stainless steel particles, was found in the suspension for injection. Potential effects: local inflammatory reactions, hypersensitivity, complications after injection of foreign bodies.

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Diprophos
Risk Level
Critical
Manufacturer
Organon Polska Sp. z o.o. ul. Marszałkowska 126/134, 00-008 Warszawa
Batch Number
U020696
EAN Code
05909990121625
Recall Date
31.01.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use the withdrawn batches of the medicine. Patients who have packs with the listed batch numbers should check the labelling, stop using the product and consult a doctor or pharmacist regarding ...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of the medicinal product Diprophos from the entire Polish market 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: A possible occurrence of brown particles with a metallic appearance, identified as stainless steel particles, was found in the suspension for injection. Potential effects: local inflammatory reactions, hypersensitivity, complications after injection of foreign bodies.
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: U020696

Related

Other Recalled Products