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SUB-TYPE: CLASS 3 RECALL

Class 3 recall-Ramipril 1.25mg tabs

Torrent Pharma (UK) Limited is recalling certain batches of Ramipril 1.25mg tablets as a precautionary measure due to these batches having a low assay and high related substances test results after their release to the market.

 

MHRA Drug alert link: https://www.gov.uk/drug-device-alerts/class-3-medicines-recall-torrent-pharma-uk-limited-ramipril-1-dot-25mg-tablets-el-24-a-slash-05?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=37e221c3-75aa-46d3-ad81-abb2683aab40&utm_content=immediately

 

 

Pip code

Product Description

Affected Batches

1111681

RAMIPRIL TAB 1.25MG

(TORRENT PHARMA)

MG21264
MG21334
MG21335
MG221014
MG221016
MG23488
MG23489
MG23490
MG23729

6290688

 

RAMIPRIL TAB 1.25MG

(TORRENT PHARMA)

MG21264
MG21334
MG21335
MG221014
MG221016
MG23488
MG23489
MG23490
MG23729

 

Further Information

For medical information enquiries please contact APCER Life Sciences, via telephone: 0800 0885366, or email: Medinfo.Torrent@apcerls.com

For stock control enquiries please contact the Torrent Pharma (UK) Limited Customer Service & Sales Executive via telephone: 01293 574188,or email:  luke.davies@torrentpharma.co.uk  or priti.pragji@torrentpharma.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: CLASS 4 CAUTION IN USE

Class 4 caution in use-Gepretix 100mg capsules

Exeltis UK Limited has informed the MHRA regarding an inconsistency in the Patient Information Leaflet (PIL) packaged in cartons of the specified batches of Gepretix 100mg capsules.

 

MHRA drug alert date: 1st February 2024

 

MHRA drug alert link:  https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-exeltis-uk-limited-gepretix-100mg-capsules-el-24-a-slash-04#contents

 

Pip code

Product

Supplier

Affected Batches

5401419

GEPRETIX 100MG CAP

EXELTIS HEALTHCARE

LF32022A
LF32119A
LF32120A
LF33488A
LF33513A

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For medical information enquiries please contact Uk.medinfo@exeltis.com or telephone 01494411775.

For stock control enquiries please contact uk.office@exeltis.com

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 caution in use- Pantoprazole 40mg Gastro resistant tablets

Crescent Pharma Limited has informed the MHRA regarding an error with the European Article Number (EAN) barcode on the cartons of the above-mentioned batches of Pantoprazole 40 mg Gastro-Resistant Tablets distributed by Crescent Pharma Limited.

 

MHRA drug alert date: 30th January 2024

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-cadila-pharmaceuticals-uk-limited-pantoprazole-40-mg-gastro-resistant-tablets-el-24-a-slash-03?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=65c56ca6-e713-4ca4-9ffd-014847ff9cd3&utm_content=immediately

 

Pip code

Product

Supplier

Affected Batches

1159664

PANTOPRAZOLE EC TAB 40MG ALM

ALMUS PHARMACEUTICALS LTD

ET571E3001
ET571E3002
ET571E3003
ET571E3004
ET571E3005
ET571E3006
ET571E3007
ET571E3008

1123850

PANTOPRAZOLE TAB 40MG ACC

ACCORD SCHEME

ET571E3001
ET571E3002
ET571E3003
ET571E3004
ET571E3005
ET571E3006
ET571E3007
ET571E3008

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For medical information enquiries please contact pharmacovigilance-eu@cadilapharma.com or telephone: +44 1217901596

For stock control enquiries please contact info@crescentpharma.com or telephone: 01256 772730

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 caution in use-Sugammadex 100 mg/ml solution for injection (2 ml vial)

USV UK Limited has informed the MHRA that Sugammadex 100 mg/ml solution for injection (2 ml vial), batch number 35000347, may contain some vials that contain a low volume of solution; less than the label claim of 2 ml.

 

 

MHRA drug alert date: 18th January 2024

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-usv-uk-limited-sugammadex-100-mg-slash-ml-solution-for-injection-2-ml-vial-el-24-a-slash-02?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=0b5575da-3811-4212-b5f0-7d8d33ce231e&utm_content=immediately

 

Pip code

Product

Supplier

Affected Batches

8062242

SUGAMMADEX SOD INJ 100MG/1ML

NOVUMGEN LTD GENERICS

35000347

1266741

SUGAMMADEX INJ 100MG/ML TEV

TEVA UK LTD

35000347

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For medical information enquiries please contact medical info at USV on medicalinfo@usvuk.com or phone: 00 800 89013370

 

For stock control enquiries please contact Novumgen on tapan.parmar@novumgen.uk or phone: 0203 096 6496 on extension 5 (Please note Novumgen is the first-line distributor of USV UK products in the UK).

SUB-TYPE: COMPANY-LED RECALL

Company led recall - NUTRAMIGEN 1 WITH LGG & NUTRAMIGEN 2 WITH LGG

 

Reckitt UK Health/Mead Johnson Nutrition have informed us of an issue regarding some batches of their product Reckitt UK Health/Mead Johnson Nutrition

 

PIP CODE

DESCRIPTION

SUPPLIER

AFFECTED BATCH

0198861

NUTRAMIGEN 1 WITH LGG, 400 g

Reckitt UK Health/Mead Johnson Nutrition

ZL3F7D

2987766

NUTRAMIGEN 2 WITH LGG, 400 g

Reckitt UK Health/Mead Johnson Nutrition

ZL3FAA

ZL3FDM

 

Reason: “A voluntary product recall involving one (1) batch of Nutramigen LGG Stage 1 Hypoallergenic Infant Formula Power and two (2) batches of Nutramigen LGG Stage 2 Hypoallergenic Infant Formula Power (product details below). This action was taken due to a possibility of cross contamination with Cronobacter sakazakii. All product distributed went through extensive testing by Reckitt/Mead Johnson Nutrition and tested negative for the bacteria.”

 

Further Information

For medical information enquiries, please call +44 (0)1895 230575 or email ConsumerNutrition_GB@rb.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.

 

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: FIELD SAFETY NOTICE

Field Safety Notice- Viscopaste Bandage 4948 7.5CMX6M

We have received a Recall from EVOLAN PHARMA on VISCOPASTE BANDAGE 4948 7.5CMX6M

 

Date of recall: 21st December 2023

 

MHRA FSN Link: https://www.gov.uk/drug-device-alerts/field-safety-notices-fsns-from-18-to-22-december-2023

Pip code

Product description

Supplier

Batch Numbers

0332734

VISCOPASTE BNDG 4948 7.5CMX6M

EVOLAN PHARMA (MEDICAL)

D300381

 

 

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 3 RECALL

Class 3 recall- Posaconazole Biocon 100mg Gastro-resistant Tablets

Biocon Pharma UK Limited are recalling a specific of batch Posaconazole 100mg Gastro-resistant Tablets due to an out of trend result for unspecified impurities during testing for stability.

 

MHRA Drug alert link: https://www.gov.uk/drug-device-alerts/class-3-medicines-recall-biocon-pharma-uk-ltd-dot-posaconazole-biocon-100mg-gastro-resistant-tablets-el-23-a-slash-44

 

Pip code

Product Description

Affected Batches

ALLIANCE DO NOT STOCK

POSACONAZOLE GR TAB 100MG

BF22004504

 

 

 

Further information

For product quality complaints and medical information enquiries contact PQCSMV@biocon.com. For reporting adverse events contact drugsafety.smv@biocon.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.

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 Caution in use-Clobazam suspension 5mg/5ml & 10mg/5ml

Atnahs Pharma UK Ltd has informed the MHRA that the batches of Clobazam Atnahs 5mg/5ml and 10mg/5ml Oral Suspension listed in this notification do not contain the most up to date safety information.

 

MHRA drug alert date: 13th December 2023

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-atnahs-pharma-uk-limited-clobazam-atnahs-5mg-slash-5ml-and-10mg-slash-5ml-oral-suspension-el-23-a-slash-43?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=d9cfeb7b-3172-4a81-9b19-60e910ea91a1&utm_content=immediately

 

Pip codes

Product

Supplier

Affected Batches

1264167

1264175

8050213

8050221

8019606

8443285

8460792

CLOBAZAM SUSP 5MG/5Ml

ATNAHS PHARMA LTD

230001

8443277

8442642

8019614

1264183

1264191

8050239

8050247

CLOBAZAM SUSP 10MG/5Ml

ATNAHS PHARMA LTD

230002

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For more information, or medical information queries, please contact +44 (0) 1268 943 700, and for stock control queries, please contact +44 (0) 1268 943 700.

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 caution in use- Clarithromycin 250mg and 500mg

Strandhaven Limited t/a Somex Pharma has informed the MHRA regarding an error with the Patient Information Leaflets (PILs) that have been packed in the listed batches of Clarithromycin 250mg and 500mg film-coated tablets.

 

MHRA drug alert date: 6th December 2023

 

MHRA drug alert link:  https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-strandhaven-ltd-t-slash-a-somex-pharma-clarithromycin-250mg-and-500mg-film-coated-tablets-el-23-a-slash-42

 

Pip code

Product

Supplier

Affected Batches

1178425

CLARITHROMYCIN TAB 250MG ACC

SOMEX/STRANDHAVEN

SEE ABOVE LINK

1148766

CLARITHROMYCIN TAB 250MG ALM

SOMEX/STRANDHAVEN

SEE ABOVE LINK

1178433

CLARITHROMYCIN TAB 500MG ACC

SOMEX/STRANDHAVEN

SEE ABOVE LINK

1148774

CLARITHROMYCIN TAB 500MG ALM

SOMEX/STRANDHAVEN

SEE ABOVE LINK

8112807

OTCD CLARITHROMYCIN TAB 250MG

SOMEX/STRANDHAVEN

SEE ABOVE LINK

8082463

OTCD CLARITHROMYCIN TAB 500MG

SOMEX/STRANDHAVEN

SEE ABOVE LINK

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For more information, medical information queries, contact: regulatory@somexpharma.com, tel: 020 8590 9399, choose option 3 or 4.

 

For stock control queries, contact: accounts@somexpharma.com, tel: 020 8590 9399, choose option 2.

SUB-TYPE: CLASS 4 CAUTION IN USE

Class 4 caution in use- Tramadol 50mg capsules

Strandhaven Limited t/a Somex Pharma has informed the MHRA regarding an error with the Patient Information Leaflets (PILs) that have been packed in the listed batches of Tramadol Hydrochloride 50mg Capsules, Hard

 

 

MHRA drug alert date: 6th December 2023

 

MHRA drug alert link:https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-strandhaven-ltd-t-slash-a-somex-pharma-tramadol-hydrochloride-50mg-capsules-hard-el-23-a-slash-41?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=58cc3b9b-942b-448f-8503-aaeab8d73d7d&utm_content=immediately

 

Pip code

Product

Supplier

Affected Batches

1115898

TRAMADOL CAP 50MG ALM (100)

STRANDHAVEN/SOMEX

SEE ABOVE LINK

1140128

TRAMADOL CAP 50MG ALM (30)

STRANDHAVEN/SOMEX

SEE ABOVE LINK

1065986

TRAMADOL CAP 50MG ACC (100)

STRANDHAVEN/SOMEX

SEE ABOVE LINK

1085463

TRAMADOL CAP 50MG ACC (30)

STRANDHAVEN/SOMEX

SEE ABOVE LINK

8082745

OTCD TRAMADOL CAP 50MG (30)

STRANDHAVEN/SOMEX

SEE ABOVE LINK

8113250

OTCD TRAMADOL CAP 50MG (100)

STRANDHAVEN/SOMEX

SEE ABOVE LINK

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For more information, medical information queries, contact: regulatory@somexpharma.com, tel: 020 8590 9399, choose option 3 or 4.

 

For stock control queries, contact: accounts@somexpharma.com, tel: 020 8590 9399, choose option 2.