SUB-TYPE: COMPANY-LED RECALL
The importer and distributor of the below products (Eaststone Limited) has informed us of reports that two affected batches may be contaminated with mould. Therefore, these batches are being recalled as a precautionary measure. This recall is being issued as a company-led recall due to the limited number of packs distributed, and Eaststone Limited have full traceability of the onward distribution by their customers.
Please can you ensure that your stores quarantine the product listed below
Pip code | Product | Supplier | Affected Batches |
Alliance do not stock | Noidecs T20/C4 (THC 20%; CBD 4%) Sativa Cannabis Flower | Eaststone Limited | 14NS2021002 |
Alliance do not stock | Noidecs T20/C4 (THC 20%; CBD 4%) Indica Cannabis Flower | Eaststone Limited | 14NI2021002 |
Alliance do not stock these products and therefore we are not accepting stock returns.
Company Contact for medical information enquiries
For medical information enquiries, please contact: Omair Sattar
Email: omair.sattar@eaststone.co.uk
Tel: 01942 841 704
Company Contact for stock enquiries
For stock information enquiries, please contact: Omair Sattar
Email: omair.sattar@eaststone.co.uk
Tel: 01942 841 704
SUB-TYPE: CLASS 3 RECALL
Advanz Pharma is recalling the below batches of Carbimazole tablets as a precautionary measure, due to an out of specification observation for tablet appearance of samples during routine stability testing. Based on the investigation performed, the observed defect was related to oxidation of the excipient red iron oxide on the surface of the tablets, due to a lack of proper mixing during the manufacturing process. There is no safety or efficacy issues as a result of this observation.
Pip code | Product description | Supplier | Batch Numbers |
8127730 | CARBIMAZOLE TAB 10MG | ADVANZ PHARMA | 120963 121025 |
1233931 | CARBIMAZOLE TAB 10MG | ADVANZ PHARMA | 120963 121025 |
8127938 | CARBIMAZOLE TAB 15MG | ADVANZ PHARMA | 120967 121028 |
Further Information
For more information or medical information queries please contact +44 (0) 8700 70 30 33 , or email medicalinformation@advanzpharma.com.
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
If you have any questions, then please contact your local Service Centre Customer Services team.
SUB-TYPE: COMPANY-LED RECALL
Advanced Accelerator Applications Ltd is recalling the below batch of LysaKare 25 g / 25 g solution for infusion (PLGB 35145/0005) as it was identified during the inspection process by the manufacturer that a small number of bags were observed to be leaking..”
Pip code | Product description | Supplier | Batch numbers |
Alliance do not stock | LYSAKARE 25 G / 25 G SOLUTION FOR INFUSION | ADVANCED ACCELERATOR APPLICATIONS (UK & IRELAND) LTD | 210155 |
Alliance do not stock this product and therefore we are not accepting stock returns.
Company contact for medical information enquiries
For medical information enquiries, please contact: Advanced Accelerator Applications (UK & Ireland) Ltd infomed@adacap.com.
Company contact for stock enquiries
For stock information enquiries contact Advanced Accelerator Applications (UK & Ireland) Ltd by emailing: customersvc.aaauk@novartis.com, tel. +44(0)20 72585200
If you have any questions, then please contact your local Service Centre Customer Services team.
SUB-TYPE: FIELD SAFETY NOTICE
The product recall for the affected batch is due to the incorrect shipment of products intended for the Belgian market to the UK/Ireland markets. As a result part of the shipments for batch 520 of Artelac Rebalance contain products with German/French/Dutch labelling. The labelling and Instructions for Use should be understood by all users in their country official language. Therefore German/French/Dutch labelled products must not be distributed in UK or Ireland
MHRA drug alert link: N/A
Pip code | Product description | Supplier | Batch numbers |
3620549 | ARTELAC REBALANCE 10ML | BAUSCH & LOMB | LOT 520 |
If you have any questions, please contact Bausch + Lomb Customer Service.
Email: Pharma_CS@bausch.com
Phone: 0845 602 2350
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.
If you have any questions, then please contact your local Service Centre Customer Services team.
SUB-TYPE: CLASS 2 RECALL
AstraZeneca UK Limited is recalling the below batch of Bricanyl 0.5mg/ml solution for injection or infusion as a precautionary measure due to out of specification results for a routinely tested known impurity during stability testing
Pip code | Product description | Supplier | Batch Numbers |
0035188 | BRICANYL AMP 0.5MG/1ML | ASTRAZENECA | F1029-1 |
Please note that Alliance Healthcare do not stock and we are therefore not accepting stock returns.
For more information or medical information queries please contact
Tel: +44 (0) 0800 783 0033
Email: medical.informationuk@astrazeneca.com
For supply queries, please contact
Tel: +44 (0) 800 783 0033 (option 1)
Email: supply.chain@astrazeneca.com.
SUB-TYPE: FIELD SAFETY NOTICE
: B. Braun have detected new additional batches where the adhesive could not polymerize completely after its application. The tested products did not show the normal curing behaviour, providing lower adhesive forces than expected.
MHRA drug alert link: N/A
Pip code | Product description | Supplier | Batch numbers | |||||||||||||||||
0416024 | HISTOACRYL ADH TISSUE BLU | BRAUN B MEDICAL |
|
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.
If you have any questions, then please contact your local Service Centre Customer Services team
SUB-TYPE: CLASS 4 CAUTION IN USE
: Lupin Healthcare (UK) Limited has informed us of a discrepancy with the product packaging for several batches of Syonell 250mg Gastro-Resistant Tablets and Syonell 500mg Gastro-Resistant Tablets. This discrepancy relates to the incorrect amount of active pharmaceutical ingredient (valproate semisodium) printed on the outer packaging
Pip code | Product description | Supplier | Batch Numbers |
4140760 | VALPROIC ACID (SYONELL) 250MG | LUPIN HEALTHCARE (UK) LTD | PLEASE FOLLOW MHRA LINK |
4140778 | VALPROIC ACID (SYONELL) 500MG | LUPIN HEALTHCARE (UK) LTD | PLEASE FOLLOW MHRA LINK |
This may have been supplied by AHDL. Unfortunately we are not providing specific batch information you will be required to follow the instructions as per the drug alert.
This is a caution in use only we are not accepting stock returns.
For more information or medical information queries, please contact: +44 (0) 1565 751 378 Option 1 or Pharmacovigilance Department at EU-PV@lupin.com
For stock control queries, please contact: 44 (0) 1565 751 378 Option 2 or information@lupin.com
If you have any questions, then please contact your local Service Centre Customer Services team.
SUB-TYPE: CLASS 2 RECALL
The recall of SMA Wysoy is a food safety recall due to potential presence of foreign bodies (pieces of plastic scoops). Nestlé has undertaken it on a voluntary basis.
The affected products' details are as follows:
PIP Code | Product Description | Supplier | Affected Batches |
4086567 | SMA WYSOY SOYA INFANT FORMULA 800G | NESTLE NUTRITION (MOV) | 024957651Z 015757651Z 000957651Z 928957651Z 923357651Z |
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
The recall of SMA Wysoy is a food safety recall due to potential presence of foreign bodies (pieces of plastic scoops). Nestlé has undertaken it on a voluntary basis.
The affected products' details are as follows:
PIP Code | Product Description | Supplier | Affected Batches |
4086567 | SMA WYSOY SOYA INFANT FORMULA 800G | NESTLE NUTRITION (MOV) | 025057651Z 025057652Z 025157651Z |
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 4 CAUTION IN USE
Macarthys Laboratories Limited T/A Martindale Pharma has informed us that the EAN barcode on the outer carton of the above batch is incorrect. When scanned, the incorrect barcode shows the batch as Martindale Pharma’s Methylthioninium Chloride Injection 1% 10 X 10ml, which has been discontinued. All other information on the outer carton (including the 2D code), as well as the immediate packaging, is correct.
The affected products' details are as follows:
PIP Code | Product Description | Supplier | Affected Batch |
ALLIANCE DO NOT STOCK | CAFFEINE CITRATE 10MG/ML SOLUTION FOR INJECTION | MACARTHYS LABORATORIES LIMITED T/A MARTINDALE PHARMA | 0134161 |
Please note that Alliance Healthcare do not stock and we are not accepting stock returns.
For more information or medical information queries, please contact: medinfo@ethypharm.co.uk
For stock control queries, please contact: Alan.josiah@ethypharm.com