TRAMADOL SYNTEZA

GIF decision: Marketing prohibition

What does this decision mean?

  • Zakaz wprowadzania — Selected batches are subject to a marketing prohibition — the product cannot be distributed to pharmacies.

Incorrect labelling of the expiry date on the outer packaging could mislead regarding the actual shelf life of the product, and the lack of recertification after repackaging means the product reached the market without full quality verification. Potential effects: lack of treatment efficacy or increased risk of adverse reactions when using the product after the true expiry date.

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TRAMADOL SYNTEZA
Risk Level
Medium
Manufacturer
Przedsiębiorstwo Farmaceutyczno-Chemiczne SYNTEZA Sp. z o.o.
Batch Number
091016
Notice Date
26.04.2019
View official statement
Source: GIF view the official alert

What to do if you have this product?

A recall means the product may be unsafe. Here is what to do if you have it at home.

  1. 1

    Do not eat or use the product

    Stop using or consuming it immediately and keep it out of reach of children.

  2. 2

    Check the batch number and expiry date

    Compare the batch/lot number and the best-before or expiry date with the details in the alert — sometimes only specific batches are affected.

  3. 3

    Return it to the shop

    You can take the product back to the shop where you bought it. For a safety recall a refund is due even without a receipt.

  4. 4

    Get help and report it

    If you feel unwell after using the product, contact a doctor. You can also report the case to the relevant authority — GIS, GIF or UOKiK.

General guidance for recalled products in Poland. Always follow the specific instructions in the official alert and from the manufacturer or retailer.

Important Information

What You Should Know

Recommendations

Do not use the product from batch 091016, check the batch number and expiry date on the packaging; if you possess this product, return it to the pharmacy or wholesaler and, in case of doubts, consult ...

Actions Taken

The Chief Pharmaceutical Inspector decided to withdraw Spasmolina 60 mg hard capsules, batch number 091016, from the market due to labelling non-compliance and the lack of recertification and batch re...

Need Help?

If you feel unwell after consuming this product, contact your doctor or call the poison control center.

Related

Other Notices