Medicines recallMHRA
T/A SyriMed, Baclofen 10mg/5ml Oral Solution recalled over a quality concern
Syri Limited, T/A SyriMed is recalling this batch of product as a precautionary measure due to crystallisation observed over time in the oral solution.
Check your product
Only products that match these details are covered. Have your pack in front of you.
4 identifiers listed for this notice.
T/A SyriMed, Baclofen 10mg/5ml Oral Solution 150 ml
- Batch codePrinted on the pack, often next to the date mark. It may start with L or LOT.
- EBB23004A1
- Product licenceThe PL number on the carton.
- PL 39307/0090
- ExpiryOn the carton, blister or label.
- 31 May 2025
- First distributedOn the product, its label or its packaging.
- 15 Jul 2024
What to do now
The MHRA has issued a notice about T/A SyriMed, Baclofen 10mg/5ml Oral Solution.
- Do not stop taking a prescribed medicine without advice: missing doses can be more dangerous than the defect.
- Compare the batch number printed on the box or label with the batches listed here.
- If your pack is affected, take it to your pharmacy or contact the prescriber for a replacement.
- Any side effect you think is linked can be reported through the Yellow Card scheme.
Why it matters. The MHRA classifies medicines recalls from Class 1 (most serious) to Class 4 (caution in use). The notice below sets out the details.
Symptoms and when to get help
Look out for
- a side effect you have not had before
- your condition not being controlled as well as usual
Get help urgently
- signs of a severe allergic reaction, such as swelling of the face or throat or difficulty breathing — call 999
- if you feel unwell and are worried, speak to a pharmacist, your GP or NHS 111
This is general information based on NHS public guidance, not medical advice. In an emergency call 999. For urgent advice use NHS 111 (NHS 24 on 111 in Scotland) or, in Northern Ireland, your GP or out-of-hours service.
Replacements and prescriptions
If your pack is affected, your pharmacy can usually exchange it for an unaffected batch or another suitable product. Prescription medicines are replaced through your pharmacy or prescriber; you do not need to buy a new supply yourself.
Many recalls are made at pharmacy or wholesaler level and do not require patients to act. The notice says which level applies.
From the official notice
Published by the Medicines and Healthcare products Regulatory Agency (EL(24)A/56). Quoted as issued.
Summary
Syri Limited, T/A SyriMed is recalling this batch of product as a precautionary measure due to crystallisation observed over time in the oral solution.
The risk
DMRC reference number DMRC-33999722 Company name
Advice for healthcare professionals
Stop supplying the above batch immediately. Quarantine all remaining stock and return it to your supplier using your supplier’s approved process.
No further action is required by patients as this is a pharmacy and wholesaler level recall. Patients should continue to take medicines from this batch as prescribed by your healthcare professional.
Do not stop taking baclofen suddenly without medical advice as you may get withdrawal side effects.
Patients who experience adverse reactions or have any questions about the medication, should seek medical attention. Any suspected adverse reactions should also be reported via the MHRA Yellow Card scheme .
Advice for patients
No further action is required by patients as this is a pharmacy and wholesaler level recall. Patients should continue to take medicines from this batch as prescribed by your healthcare professional.
Do not stop taking baclofen suddenly without medical advice as you may get withdrawal side effects.
Patients who experience adverse reactions or have any questions about the medication, should seek medical attention. Any suspected adverse reactions should also be reported via the MHRA Yellow Card scheme .
Open the MHRA notice
Questions
Why has T/A SyriMed, Baclofen 10mg/5ml Oral Solution been recalled?
The MHRA has issued a notice about T/A SyriMed, Baclofen 10mg/5ml Oral Solution. The MHRA classifies medicines recalls from Class 1 (most serious) to Class 4 (caution in use). The notice below sets out the details.
How do I know if my medicine is affected?
Compare the batch code, product licence, expiry and date code on your pack with the details listed under “Check your product” on this page. Only items that match are covered by the notice.
What should I do now?
Do not stop taking a prescribed medicine without advice: missing doses can be more dangerous than the defect. Compare the batch number printed on the box or label with the batches listed here.
Do I need a new prescription?
If your pack is affected, your pharmacy can usually exchange it for an unaffected batch or another suitable product. Prescription medicines are replaced through your pharmacy or prescriber; you do not need to buy a new supply yourself. Many recalls are made at pharmacy or wholesaler level and do not require patients to act. The notice says which level applies.