SUB-TYPE: CLASS 4 CAUTION IN USE
Martindale Pharma has made the MHRA aware that the GTIN in the 2D barcode and the printed variable data represents the branded version of the product (Venlalic® XL 300 mg prolonged-release tablets).
MHRA drug alert date: 16 November 2022
Pip code | Product description | Supplier | Batch Numbers |
8047318 1257559 8045320 | VENLAFAXINE XL TAB 300MG | MARTINDALE PHARMA | LC69391 |
This is a caution in use only we are not accepting stock returns - if any defective stock is found it should be returned directly to the manufacturer.
Further Information
For further information, medical enquiries and stock information, contact: Licensed@ethypharm.com
Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.
SUB-TYPE: CLASS 4 CAUTION IN USE
Macarthys Laboratories (trading as Martindale Pharma, an Ethypharm Group Company), has notified the MHRA of a limited number of Prenoxad packs in a batch marketed in France with missing needles.
MHRA drug alert date: 10th November 2022
Pip code | Product description | Supplier | Batch Numbers | ||||||||||||||||||||||||
3797131 | PRENOXAD 1MG/ML INJECTION | ETHYPHARM GROUP COMPANY |
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This is a caution in use only we are not accepting stock returns - if any defective stock is found it should be returned directly to the manufacturer.
Further Information
For more information on licensed stock and resupply queries for the licensed presentation, please contact licensed@ethypharm.com; telephone number: 0800 028 7933.
For medical information queries and all other enquiries, please contact medinfo@ethypharm.com; telephone number 01277 266 600.
Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.
SUB-TYPE: COMPANY-LED RECALL
L&R medical have informed us that on the affected batch of Activa Thigh Length Open Toe Hosiery XL the product inside the packaging is Small and not Extra Large
MHRA drug alert link: N/A
PIP CODE | DESCRIPTION | SUPPLIER | AFFECTED BATCHES |
2590883 | ACTIVA T/L O/T C2 SND XL | L&R MEDICAL UK LTD | 221909 |
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.
For more information please contact L&R MEDICAL UK LTD
Quality&Regulatory@uk.lrmed.com
SUB-TYPE: CLASS 3 RECALL
Medreich Plc UK is recalling the above batch as a precautionary measure due to out of specification results for tablet dissolution during routine product release testing.
MHRA drug alert date: 27th October 2022
Pip code | Product description | Supplier | Batch Numbers |
1152123 | MEBEVERINE TAB 135MG | MEDREICH PLC | B11539 |
1037514 | MEBEVERINE TAB 135MG | MEDREICH PLC | B11539 |
8113110 | OTCD MEBEVERINE TAB 135MG | MEDREICH PLC | B11539 |
Further Information
For more information or supply enquiries, please contact Medreich PLC at cs_team@medreich.co.uk or by phone at 0208 831 1580, 0208 831 1511 or 0208 831 1509
For medical information queries, please contact pharmacovigilance@medreich.com
Recipients of this Medicines Recall should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.
SUB-TYPE: CLASS 4 CAUTION IN USE
Recordati Rare Diseases T/A Recordati Rare Diseases UK Ltd has made the MHRA aware that specific batches of Pedea 5 mg/ml solution for injection have been packaged with the incorrect Product Information Leaflet (PIL).
MHRA drug alert date: 25th October 2022
MHRA drug alert link:
Pip code | Product description | Supplier | Batch Numbers |
ALLIANCE DO NOT STOCK | PEDEA 5 MG/ML SOLUTION FOR INJECTION, 4 AMPOULES | RECORDATI RARE DISEASES T/A RECORDATI RARE DISEASES UK LTD | PD0G24E-07 PD0G24E-10 PF0G04E-03 |
This is a caution in use only we are not accepting stock returns - if any defective stock is found it should be returned directly to the manufacturer.
For further information, including medical enquiries and stock information, please contact:
Recordati Rare Diseases UK Ltd (local representative, WDA(H): 15720) on Tel: +44 (0)1491 414333 or +33 1 47 73 64 58 or email: RRDmedinfo@recordati.com
Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to hospital pharmacists and pediatric doctors and nurses working in hospital setting for information.
SUB-TYPE: CLASS 1 RECALL
Sanofi UK is initiating an urgent recall of the above batches of Targocid 200mg powder for solution for injection/infusion or oral solution.
This is due to out of specification results obtained for bacterial endotoxins, which has been confirmed through testing of retain samples. This issue was observed following a medical adverse event, which reported that four patients experienced high grade of fever approximately three hours post-administration of vials from the impacted batches.
Due to the out of specification results observed there is a potential life threatening or serious risk to patient health.
MHRA drug alert date: 21st October 2022
MHRA drug alert link:
Pip code | Product Description | Supplier | Batch Numbers |
ALLIANCE DO NOT STOCK | TARGOCID 200MG POWDER FOR SOLUTION FOR INJECTION/INFUSION OR ORAL SOLUTION | AVENTIS PHARMA LIMITED T/A SANOFI | 0J25D1 0J25D2 |
Alliance do not stock the above products so we will not be accepting Customer returns on this recall.
Further information
For more information on licensed stock and resupply queries for the licensed presentation, please contact GB-CustomerServices@sanofi.com; phone number: 0800 854 430.
For medical information queries and all other enquiries, please contact uk-medicalinformation@sanofi.com; phone number: 0800 035 25 25.
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.
SUB-TYPE: CLASS 2 RECALL
hameln pharma ltd is initiating a recall of the affected batches of Ephedrine Hydrochloride 30 mg/ml Solution for Injection as a precautionary measure.
MHRA drug alert date: 20 October 2022
Pip Code | Product Description | Supplier | Batch Numbers |
ALLIANCE DO NOT STOCK | EPHEDRINE HYDROCHLORIDE 30MG/ML SOLUTION FOR INJECTION | HAMELN PHARMA LTD |
11081120C 04600520C |
Alliance do not stock the above products so we will not be accepting Customer returns on this recall.
For more information or supply queries, please contact or email hameln pharma ltd customer services on +44 (0)1452 621 661 or customer.services@hameln-pharma.co.uk
For medical information queries, please contact or email hameln pharma ltd Medicines Information on +44 (0)1452 621 661 or drug.safety@hameln-pharma.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.
SUB-TYPE: COMPANY-LED RECALL
Viatris have informed that product Endwarts Freeze® has been manufactured with 5 tips instead of the stipulated 7 as indicated on the packaging and leaflet.
MHRA drug alert link: N/A
PIP CODE | DESCRIPTION | SUPPLIER | AFFECTED BATCHES |
4044368 | ENDWARTS FREEZE 7.5g | VIATRIS UK HEALTHCARE | 260222C08 |
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.
For more information please contact VIATRIS UK HEALTHCARE
Gary Marshall Gary.marshall@viatris.com 07817 486960
SUB-TYPE: CLASS 4 CAUTION IN USE
Flamingo Pharma UK Ltd has identified an error relating to the ink printing of the batch number and expiry date on the carton for three batches of Ibuprofen 400mg Tablets. This notification includes all potentially impacted products/batches.
MHRA drug alert date: 12th October 2022
MHRA drug alert link:
Pip code | Product description | Supplier | Batch Numbers | ||
ALLIANCE DO NOT STOCK | IBUPROFEN 400MG TABLETS | FLAMINGO PHARMA |
| ||
ALLIANCE DO NOT STOCK | IBUPROFEN 400MG TABLETS | FLAMINGO PHARMA |
|
This is a caution in use only we are not accepting stock returns - if any defective stock is found it should be returned directly to the manufacturer.
Further Information
For medical information and stock control queries please contact:
Flamingo Pharma
For medical information safety@flamingopharma.co.uk or general product enquiry sales@flamingopharma.co.uk +44 (0) 7733522465
Or
Mawdsley Brooks & Co Ltd
Overlabellingcustomerservices@mawdsleys.co.uk 01302 553064
Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.
SUB-TYPE: CLASS 2 RECALL
hameln pharma ltd is initiating a recall of batch 210505 of Amiodarone Hydrochloride 50 mg/ml Concentrate for Solution for Injection/Infusion as a precautionary measure. This is due to an increased presence of visible crystalline particles within the solution, identified during ongoing re-inspection of retained samples.
MHRA drug alert date: 11 October 2022
Pip Code | Product Description | Supplier | Batch Numbers |
ALLIANCE DO NOT STOCK | AMIODARONE HYDROCHLORIDE 50MG/ML SOLUTION FOR INJECTION/INFUSION | HAMELN PHARMA LTD | 210505 |
Alliance do not stock the above products so we will not be accepting Customer returns on this recall.
For more information or supply queries, please contact or email hameln pharma ltd customer services on +44 (0)1452 621 661 or customer.services@hameln-pharma.co.uk
For medical information queries, please contact or email hameln pharma ltd Medicines Information on +44 (0)1452 621 661 or drug.safety@hameln-pharma.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.