Medicines recallMHRA
ChloraPrep 1mL applicator recalled over possible contamination
Becton Dickinson UK Ltd are recalling batches of ChloraPrep 2% w/v / 70% v/v cutaneous solution 1mL applicators due to a potential breach of sterility in the packaging process.
Check your product
Only products that match these details are covered. Have your pack in front of you.
ChloraPrep 1mL applicator ChloraPrep 1mL Applicator: 60 applicators
- First distributedOn the product, its label or its packaging.
- 25/06/2025
- Affected
- All lots with an expiry date up to and including 05/2029*
What to do now
Affected batches of ChloraPrep 1mL applicator may be contaminated, for example with particles or microorganisms.
- 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. Contamination matters most for injections, eye drops and products used on broken skin, where it could cause infection.
Symptoms and when to get help
Look out for
- redness, swelling or pain where the product was used
- a high temperature
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(26)A/34). Quoted as issued.
Summary
Becton Dickinson UK Ltd are recalling batches of ChloraPrep 2% w/v / 70% v/v cutaneous solution 1mL applicators due to a potential breach of sterility in the packaging process.
The risk
DMRC reference number DMRC - 40102707 Marketing Authorisation Holder
Advice for healthcare professionals
Stop supplying the affected batches. 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 product is used by healthcare professionals and they will have taken the action to remove this product from use.
The recall is a precautionary measure to mitigate any additional risk of infection.
Patients who experience adverse reactions or have any questions about their 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 product is used by healthcare professionals and they will have taken the action to remove this product from use.
The recall is a precautionary measure to mitigate any additional risk of infection.
Patients who experience adverse reactions or have any questions about their 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 ChloraPrep 1mL applicator been recalled?
Affected batches of ChloraPrep 1mL applicator may be contaminated, for example with particles or microorganisms. Contamination matters most for injections, eye drops and products used on broken skin, where it could cause infection.
How do I know if my medicine is affected?
Compare the 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.