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WARNING: RECALLED PRODUCT
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Detimedac 500 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, possible adverse reactions.

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Detimedac 500 mg
Risk Level
Critical
Manufacturer
medac Gesellschaft für klinische Spezialpräparate mbH z siedzibą w Niemczech
Batch Number
G220299AD
EAN Code
05909991029708
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 on the packaging and, if you have this medicine, return it to the pharmacy and consult your doctor about further treatment.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of the medicinal product from the market throughout the country and granted the decision immediate enforceability; the marketing autho...

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, possible adverse 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: G220299AD

Related

Other Recalled Products