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WARNING: RECALLED PRODUCT
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Vendal retard

Due to morphine being released in a different amount than specified in the documentation, the impact on the course of therapy and the suspicion of a threat to the patient’s health or life cannot be excluded. Potential effects: overdose or insufficient analgesic effect, dependence, life-threatening complications.

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Vendal retard
Risk Level
Critical
Manufacturer
G.L. Pharma GmbH, Schlossplatz 1, A-8502 Lannach, Austria
Batch Number
0F225A
EAN Code
05909990743926
Recall Date
28.08.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use Vendal retard from batch 0F225A, check the batch number on the packaging, return the product to the pharmacy; if this batch has been taken, consult a doctor.

Actions Taken

Withdrawal from the market throughout the entire country of batch 0F225A of Vendal retard and granting 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: Due to morphine being released in a different amount than specified in the documentation, the impact on the course of therapy and the suspicion of a threat to the patient’s health or life cannot be excluded. Potential effects: overdose or insufficient analgesic effect, dependence, life-threatening complications.
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: 0F225A

Related

Other Recalled Products