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WARNING: RECALLED PRODUCT
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Vigantol

Suspected quality defect of the medicinal product resulting from the use of an excipient linked to a batch with an out-of-specification active substance content, which may lead to incorrect dosing of vitamin D. Potential effects: lack of efficacy or adverse effects related to overdose.

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Vigantol
Risk Level
Medium
Manufacturer
P&G Health Germany GmbH
Batch Number
20CQ046
EAN Code
05909990178513
Recall Date
25.04.2022
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 200Q046, check the batch number on the packaging, and return the medicine to a pharmacy if you have it; in case of any worrying symptoms after use, contact a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch 200Q046 of Vigantol from the market throughout the country, granted the decision immediate enforceability, and obliged the marketing authorisation hol...

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: Suspected quality defect of the medicinal product resulting from the use of an excipient linked to a batch with an out-of-specification active substance content, which may lead to incorrect dosing of vitamin D. Potential effects: lack of efficacy or adverse effects related to overdose.
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: 20CQ046

Related

Other Recalled Products