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WARNING: RECALLED PRODUCT
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Detimedac 200 mg

The pink discoloration may be caused by degradation of the active substance, which may pose an increased risk to the patient. Potential effects: lack of treatment efficacy, complications of oncological therapy, possible adverse effects related to degradation products.

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Detimedac 200 mg
Risk Level
Critical
Manufacturer
medac Gesellschaft für klinische Spezialpräparate mbH z siedzibą w Niemczech
Batch Number
F220255BA
EAN Code
05909991029609
Recall Date
03.07.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the listed batches. Check the batch number of the medicine you have, and if it matches, return it to the pharmacy or your doctor. If in doubt or if the medicine from these ...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of Detimedac medicinal products from the market throughout the country and granted the decision immediate enforceability; the marketin...

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: The pink discoloration may be caused by degradation of the active substance, which may pose an increased risk to the patient. Potential effects: lack of treatment efficacy, complications of oncological therapy, possible adverse effects related to degradation products.
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: F220255BA

Related

Other Recalled Products