SUB-TYPE: CLASS 4 CAUTION IN USE
Hikma Farmacêutica (Portugal) S.A has informed the MHRA that the Patient Information Leaflet (PIL) contained within batch CB0033 of Gemcitabine 2g/52.6ml concentrate for solution for infusion does not contain the side effects of serious skin reactions.
MHRA drug alert Date: 04/09/25
MHRA drug alert link: Class 4 Medicines Defect Notification: Hikma Farmacêutica, Gemcitabine 2g/52.6ml concentrate for solution for infusion, EL(25)A/43 - GOV.UK
Pip code | Product description | Supplier | Batch Numbers |
Alliance Do Not Stock | Gemcitabine 2g/52.6ml concentrate for solution for infusion | Hikma Farmacêutica | CB0033 |
This is a caution in use only we are not accepting stock returns
further information
For medical information queries please telephone +351 21 960 8410, or email portugaleupharmacovigilance@hikma.com.
For all stock control enquiries please telephone +44 020 7399 2760, or email customerserviceuk@hikma.com
SUB-TYPE: FIELD SAFETY NOTICE
Packaging failures were identified related to the MediHoney® Wound and Burn products
Date of recall 02/09/25
Pip code | Product description | Supplier | Batch Numbers |
3141207 | MEDIHONEY WOUND GEL (SGLE USE) | INTEGRA NEUROSCIENCES LIMITED | All |
3141215 | MEDIHONEY WOUND GEL | INTEGRA NEUROSCIENCES LIMITED | ALL |
3387644 | MEDIHONEY BARRIER CREAM 50G | INTEGRA NEUROSCIENCES LIMITED | ALL |
3441490 | MEDIHONEY MEDICAL HONEY | INTEGRA NEUROSCIENCES LIMITED | ALL |
3463346 | MEDIHONEY TULLE DRSG 10CMSQ | INTEGRA NEUROSCIENCES LIMITED | ALL |
3470929 | MEDIHONEY APINATE 10CMSQ DRSG | INTEGRA NEUROSCIENCES LIMITED | ALL |
3665411 | MEDIHONEY A/B APINATE 5CMSQ | INTEGRA NEUROSCIENCES LIMITED | ALL |
3665429 | MEDIHONEY A/B APINATE 1.9X30CM | INTEGRA NEUROSCIENCES LIMITED | ALL |
3691276 | MEDIHONEY BARRIER CRM SACH | INTEGRA NEUROSCIENCES LIMITED | ALL |
3943545 | MEDIHONEY DERMA CRM | INTEGRA NEUROSCIENCES LIMITED | ALL |
Please return all affected stock to your original supplier for credit. Unfortunately we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies.
Please note that anything not returned to us, or notified to us, within 3 months of this notification, cannot be reimbursed by way of a credit.
SUB-TYPE: CLASS 4 CAUTION IN USE
Ipca Laboratories UK Ltd has informed the MHRA that the Patient Information Leaflet (PIL) in the products listed in this notification do not contain all the required safety information.
MHRA drug alert date 27/08/25
MHRA drug alert link:Class 4 Medicines Defect Notification: Ipca Laboratories UK Limited, Various Products, EL(25)A/42 - GOV.UK
Pip code | Product description | Supplier | Batch Numbers |
Multiple-see above link | see above link | see above link | see above link |
This is a caution in use only we are not accepting stock returns
Further Information
For all medical information enquiries and information on this product, please contact via email address:pharmacovigilance@ipcauk.com or via telephone: 08003685328
For stock control enquiries please contact via telephone: +44 (0)7446 189 936.
SUB-TYPE: CLASS 4 CAUTION IN USE
Class 4 caution in use - Fexofenadine Hydrochloride 120mg film-coated tablets
Chanelle Medical Unlimited Company has informed the MHRA of an error with the European Article Number (EAN) / Global Trade Item Number (GTIN) barcode on the cartons of the above batch of Fexofenadine Hydrochloride 120mg film-coated tablets, distributed by Healthcare Pharma Limited. When scanned, the EAN/GTIN barcode identifies the product as Naratriptan 2.5mg Tablets..
MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-notification-fexofenadine-hydrochloride-120mg-film-coated-tablets-chanelle-medical-unlimited-company-el-25-a-slash-41?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=6190b8e4-635d-43ca-b371-997872fb962f&utm_content=immediately
MHRA drug alert date: 21/08/25
Pip code | Product description | Supplier | Batch Numbers |
Alliance Do Not Stock | Fexofenadine Hydrochloride 120mg film-coated tablets | Chanelle Medical Unlimited Company | See link above |
This is a caution in use only we are not accepting stock returns
For all medical information enquiries and information on this product, please contact Medical Information Department chanelle@medinformation.co.uk or telephone +44 808 304 2429 (Toll free-UK).
For stock control enquiries please email David Hammond: david.hammond@healthcarepharma.co.uk. Recipients of this Medicines Recall should bring.
SUB-TYPE: CLASS 4 CAUTION IN USE
Accord Healthcare Limited, UK has informed the MHRA that the Patient Information Leaflet (PIL) and Summary of Product Characteristics (SPC) do not contain all the required safety information.
MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-notification-levetiracetam-accord-100mg-slash-ml-oral-solution-accord-healthcare-limited-uk-el-25-a-slash-40?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=9f75ebd8-3b27-4733-8087-29486e7f8a54&utm_content=immediately
MHRA drug alert date: 14/08/25
Pip code | Product description | Supplier | Batch Numbers |
1216084 | Levetiracetam Accord 100mg/ml oral solution | Accord Healthcare Limited | See link above |
This is a caution in use only we are not accepting stock returns
For medical information enquiries please contact:
Accord Medical Information Department on 01271 385257, email- medinfo@accord-healthcare.com.
For stock control enquiries please contact: Accord- Customer Services Team on 0800 373573.
SUB-TYPE:
Zydus Pharmaceuticals UK LTD has informed the MHRA that there is an error on the artwork for the outer carton and Patient Information Leaflet (PIL) of Topiramate Zydus Pharmaceuticals UK 20mg/ml Oral Solution (pack size 150ml and 280ml bottles).
MHRA drug alert link:Class 4 Medicines Defect Notification: Topiramate Zydus Pharmaceuticals UK 20mg/ml Oral Solution, Zydus Pharmaceuticals UK Ltd, EL(25)A/39 - GOV.UK
MHRA drug alert date:07/08/25
Pip code | Product description | Supplier | Batch Numbers |
8092231 | TOPIRAMATE SF SOLN 20MG/ML (150ml) | Zydus Pharmaceuticals UK LTD | TPR24003 |
8092249 | TOPIRAMATE SF SOLN 20MG/ML (280ml) | Zydus Pharmaceuticals UK LTD | TPR24001 TPR24002 |
This is a caution in use only we are not accepting stock returns
Further Information
For all enquires on this product please email DrugSafety@ZydusUK.com or telephone 0800 9956034.
SUB-TYPE: CLASS 2 RECALL
LEO Pharma is recalling the affected batch as a precautionary measure due to out of specification results for impurities during routine stability testing.
MHRA drug alert link https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-fucidin-250-mg-tablets-leo-laboratories-ltd-trading-as-leo-pharma-el-25-a-slash-38
MHRA drug alert date: 02/08/25
Pip code | Product description | Supplier | Batch Numbers |
0105452 | FUCIDIN EC TAB 250MG** | Leo Pharma | D00993 |
Further Information
For all enquiries and information on this product, please email medical-info.uk@leo-pharma.com or telephone 01844 347 333 and press 2 for Medical Information.
Please return all affected stock to your original supplier for credit. Unfortunately, we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies.
Please note that anything not returned to us, or notified to us, within 3 months of this notification, cannot be reimbursed by way of a credit.
SUB-TYPE:
To help keep our customers informed of changes to our service, we have published our August 2025 bank holiday opening hours for pharmacy and retail customers.
August 2025 bank holiday opening hours
August 2025 bank holiday opening hours (for Channel Islands and Isle of Man)
SUB-TYPE: CLASS 4 CAUTION IN USE
Jubilant Pharmaceuticals NV has informed the MHRA that the Patient Information leaflet (PIL) in the cartons for the batches listed in this notification include an outdated PIL.
MHRA drug alert link:Class 4 Medicines Defect Notification: Olmesartan medoxomil 10mg film-coated tablets, Jubilant Pharmaceuticals NV, EL(25)A/37 - GOV.UK
MHRA drug alert date:31/07/25
Pip code | Product description | Supplier | Batch Numbers |
8139206 | OLMESARTAN TAB 10MG | Jubilant Pharmaceuticals NV | MR124001A MR124002A |
8139222 | OLMESARTAN TAB 20MG | Jubilant Pharmaceuticals NV | MR224001A |
This is a caution in use only we are not accepting stock returns
Further Information
For medical information enquiries please email safety.uk@lambda-cro.com, or telephone 0800 0668348.
For stock control enquiries please email JPUK.Customerservice@jubl.com, or telephone 01233 552293
SUB-TYPE: CLASS 2 RECALL
CD Pharma Ltd have notified the MHRA of an error on the outer carton of the product for the batches listed in this notification. While the total active content statement is correct, the delivered dose content statement is incorrect. The other details on the carton are correct.
drug alert date: 24/07/25
Pip code | Product description | Supplier | Batch Numbers |
3727575 (TPOS-NOT STOCKED) | FLUTIFORM 250/10MG | CD Pharma LTD | 270185-24062FA-30424 |
Further Information
For all further enquiries please contact 01355 204 448 or email regaffairs@teleta.co.uk
Please return all affected stock to your original supplier for credit. Unfortunately, we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies.
Please note that anything not returned to us, or notified to us, within 3 months of this notification, cannot be reimbursed by way of a credit.