CLASS 2 RECALL - ABSTRAL TAB 200MCG (SCHEDULE 2 CD)

Kyowa Kirin Limited is recalling the below batches as a precautionary measure, due to the reports of double tablets in a single blister pocket. This is a follow up alert, following the issue of EL (20)A/34. Since this notification, Kyowa Kirin Limited have initiated corrective actions to resolve the issue. Complaint batches 608973601 and 608973602 were manufactured prior to the corrective actions being implemented...

This product is a Schedule 2 Controlled Drug, so please use the Returns Portal for any recalled stock you may need to return to ensure there is authorisation to return. If you are unable to use the Returns Portal then your Alliance Healthcare driver will have a ‘Specialist Product Recall Book’ with them on Thursday 26^th November and Friday 27th November  for completion and product uplift AM ONLY. Due to Covid 19, the driver will complete the form on your behalf.  They will ask for the quantity of stock you have to return and the name of the pharmacist. The driver will give you a copy of the completed form for your records.

If you need to return recalled stock from 28th November and are unable to use the Returns Portal please call Customer Services for authorisation to return.

Further Information

For Stock control enquiries please contact: Karen Murray, Commercial Manager

Telephone: +44 (0) 7712 001288

E-mail: karen.murray@kyowakirin.com

For Medical information enquiries please contact:

Medical Information Direct Line: + 44 (0)1896 664 000

E-mail: medinfo@kyowakirin.com

For Quality information please contact: Martin Smith (Responsible Person)

Telephone: +44 7904671807

E-mail: Martin.Smith@kyowakirin.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.

This recall will remain open for 3 months from the date issued unless an alternative date is agreed by instigator. The closure of this will be 25/02/2021. Please note after this date customer returns may still be accepted but customers may not be credited

CLASS 2 RECALL - ANCOTIL 2.5 G/250 ML SOLUTION FOR INFUSION

: Mylan UK Healthcare Ltd has been informed of a non-compliance event which occurred during the most recent inspection at the contract manufacturing site for the above product in relation to product sterility. As a precautionary measure, remaining stock of the above batches are being recalled.

For more information or medical information enquiries please contact Mylan UK Healthcare Ltd Medical Information Department on +44(0) 1707 853000 or via email at Info.uk@mylan.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

This recall will remain open for 3 months from the date issued unless an alternative date is agreed by instigator. The closure of this will be 12/02/2021. Please note after this date customer returns may still be accepted but customers may not be credited.

CLASS 2 RECALL - Sodiofolin 50mg/ml Solution for Injection 100mg/2ml

medac Pharma LLP is recalling the below batch of products due to some inspected vials showing hairline damage to the shoulder of the vials. So far, the company has not received any reports of damage for marketed products. However, as this defect may impact on the sterility of the product, the above batch is being recalled as a precautionary measure

Please note that Alliance Healthcare do not stock and we are not accepting stock returns.

For more information or medical information queries, please contact info@medacpharma.co.uk or telephone 01786 458086

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

If you have any questions, then please contact your local Service Centre Customer Services team

Class 4 Drug Caution in use - Kolanticon Gel

Intrapharm Laboratories Ltd has informed us that there is a difference in dosage instructions between the carton and label. The Patient Information Leaflet (PIL) and bottle label contain the correct instructions.

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: medinfo@intrapharmlabs.com or telephone +44 (0)330 1359 437.

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

If you have any questions, then please contact your local Service Centre Customer Services team

Class 3 recall - Alfad 0.25 Microgram Capsules

Further to Drug Alert EL (20)A/46 issued on 29 September 2020 Theramex Ireland Ltd T/A Theramex HQ UK Ltd has informed us of an issue related to error in the decommissioning of a further batch as listed above. Upon decommissioning at the pharmacy and when scanning the serialised 2D code, the status of packs may report as ‘EXPORT’. Although there is no risk to product quality, any remaining stock should be quarantined and returnedThe affected products' details are as follows:

Please note that Alliance do not stock the above products therefore we are not accepting returns on this recall.

For stock control enquiries please contact Theramex HQ UK Ltd Customer Services Team on 020 3962 5532.

For medical information enquiries please contact Theramex HQ UK Ltd Medical Information Department on 033 3009 6795.

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

COMPANY LED - CLASS 2 RECALL Class type: Company Led

Precautionary recall following mould being identified in a few jars of each batch.

The affected products' details are as follows:

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

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

Company Led Drug Alert Optiray 300mg & 350mg I-Ml Solution For Injection Class type: Company Led

Guerbet Laboratories Limited is recalling the above batches of products as a precautionary measure due to reports received from healthcare professionals on the difficulties in attaching the Luer lock adapter to the Luer tip of the pre-filled syringe and tubing catheter. In some cases this has resulted in leakages of contrast media during use.

The affected products' details are as follows:

Alliance do not stock these products and therefore we are not accepting stock returns.

For medical information and stock enquiries, please contact Guertbet Laboratories Limited on Tel: 01217338542

E-mail (medical enquiries): uk.sales@guerbet.com and Krupa.mehta@guerbet.com

Email (stock enquiries): uk.sales@guerbet.com

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

Field Safety Notice Activheal® Hydrogel 8g

AMS has identified that due to a tube quality issue that was determined during the manufacturing process, the sterility of a small number of the Affected Tubes may have been compromised. Investigations have determined a potential root cause and AMS are confident that the quality issue only affects the Affected Tubes and is not present in other batches of the ACTIVHEAL® Hydrogel product

The affected products' details are as follows:

This is an NWOS only recall and Alliance will not be accepting stock returns. Please contact Advanced Medical Solutions for further information

For further information regarding this Field Safety Notice Please contact Teresa Starkey at Advanced Medical Solutions. Email: Teresa.starkey@admedsol.com Tel: +441606 545617

Recipients of this Drug Alert should bring it to the attention of relevant contacts.

If you have any questions, then please contact your local Service Centre Customer Services team

Class 2 Recall on Epilim 500mg Ec Tabs

Sanofi is recalling the above batches of product as a precautionary measure due to out of specification results for disintegration test during routine stability testing.

If you have any questions, then please contact your local Service Centre Customer Services team.

Class 3 Recall on Metoprolol 50 Mg Tablets

Accord Healthcare Ltd has informed us of an issue related to decommissioning of the above batches. Upon decommissioning at the pharmacy, there have been reports stating that when scanning the serialised 2D code, the status of packs may report as ‘EXPORT.' Although there is no risk to product quality, any remaining stock should be quarantined and returned.