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WARNING: RECALLED PRODUCT
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Debridat

Risk of the presence of a foreign body in the medicinal product, possibly due to a potential quality defect. Potential effects: mechanical damage to the gastrointestinal tract, complications, need for medical intervention.

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Debridat
Risk Level
Critical
Manufacturer
Pfizer Europe MA EEIG z siedzibą w Brukseli, Belgia
Batch Number
3804
EAN Code
05902023771637
Recall Date
22.11.2019
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 it, return the product to a pharmacy or consult a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of Debridat from the market throughout the country and granted the decision immediate enforceability, obliging the company to carry ou...

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: Risk of the presence of a foreign body in the medicinal product, possibly due to a potential quality defect. Potential effects: mechanical damage to the gastrointestinal tract, complications, need for medical intervention.
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: 3804

Related

Other Recalled Products