Medicines recallMHRA
Evorel Sequi recalled over a packaging defect
Theramex has informed the MHRA that some cartons of Evorel Sequi contain the incorrect combination of patches. An error at the packaging site means that a limited number of packs have the incorrect combination of Evorel 50 and Evorel Conti patches.
Check your product
Only products that match these details are covered. Have your pack in front of you.
4 identifiers listed for this notice.
Evorel Sequi 8 patches
- Batch codePrinted on the pack, often next to the date mark. It may start with L or LOT.
- 6137001
- Product licenceThe PL number on the carton.
- PL 49105/0010
- ExpiryOn the carton, blister or label.
- September 2025
- First distributedOn the product, its label or its packaging.
- 12 April 2024
What to do now
A fault with the packaging or delivery device of Evorel Sequi has been found.
- 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. A faulty cap, seal, syringe or inhaler can mean a missed or wrong dose, or contamination of the product.
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/41). Quoted as issued.
Summary
Theramex has informed the MHRA that some cartons of Evorel Sequi contain the incorrect combination of patches. An error at the packaging site means that a limited number of packs have the incorrect combination of Evorel 50 and Evorel Conti patches.
The risk
DMRC ref DMRC-31752921 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.
If a patient presents with the incorrect patches, a replacement pack will be required. Theramex has confirmed that all other batches are unaffected and that there is no impact on supply. The Department of Health and Social Care (DHSC) has confirmed that, as this is a prescription only medicine, a new prescription will be required for the dispensing of a replacement product.
Some patients who have received this product will be entitled to free prescriptions through existing exemptions, or have arrangements in place for a HRT pre-payment certificate and therefore a new prescription will not incur any additional costs. Where patients pay for NHS prescriptions, a charge for the new prescription will apply; patients may contact the Defective Medicines Reporting Centre if further information is required.
Patients who may have received the impacted batch of Evorel Sequi should consider the following information:
Check the contents of your pack to ensure that it contains four (4) Evorel 50 patches and four (4) Evorel Conti patches. The packaging is clearly labelled with the medication names.
If you have received four (4) of each patch, please continue to take the medicine as prescribed
by your healthcare professional. You do not need to take any action.
If you do not have 4 of each patch, please contact your pharmacist for further advice and arrangement for dispensing of a replacement product.
Patients who experience adverse reactions or have any questions about the medication should seek medical attention. Any suspected adverse reactions should be reported via the MHRA Yellow Card scheme .
Advice for patients
Patients who may have received the impacted batch of Evorel Sequi should consider the following information:
Check the contents of your pack to ensure that it contains four (4) Evorel 50 patches and four (4) Evorel Conti patches. The packaging is clearly labelled with the medication names.
If you have received four (4) of each patch, please continue to take the medicine as prescribed
by your healthcare professional. You do not need to take any action.
If you do not have 4 of each patch, please contact your pharmacist for further advice and arrangement for dispensing of a replacement product.
Patients who experience adverse reactions or have any questions about the medication should seek medical attention. Any suspected adverse reactions should be reported via the MHRA Yellow Card scheme .
Open the MHRA notice
Questions
Why has Evorel Sequi been recalled?
A fault with the packaging or delivery device of Evorel Sequi has been found. A faulty cap, seal, syringe or inhaler can mean a missed or wrong dose, or contamination of the product.
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.