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Pharmaswiss 膶eska republika s.r.o. (an affiliate of Bausch & Lomb UK Limited) is recalling all unexpired batches of Emerede Adrenaline Autoinjectors after identifying an error than can cause some pens to fail to activate.
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M&A Pharmachem Limited is recalling all unexpired batches as a precautionary measure, because a small number of pots from some batches have been found to contain discoloured tablets due to fungal contamination.
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List of field safety notices (FSNs) from medical device manufacturers from 18 to 22 November 2019.
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OTC Concepts Ltd, Relonchem Ltd, Noumed Life Sciences Ltd and Medreich Plc. are recalling stock from pharmacies and retail stores as a precautionary measure due to possible contamination with an impurity.
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Creo Pharma Limited and Tillomed Laboratories Limited are recalling all unexpired stock of the products listed in this alert.
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List of field safety notices (FSNs) from medical device manufacturers from 11 to 15 November 2019.
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Accord-UK Ltd has informed us of an issue related to decommissioning of the batch below.
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List of field safety notices (FSNs) from medical device manufacturers from 04 to 08 November 2019
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Sandoz Limited is recalling one batch due to the occurrence of degradation in some vials, resulting in green discoloration of the powder in the vial, leading to increased levels of impurities/degradation products in the medi鈥�
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This recall affects Mitomycin-C Kyowa 2 mg (PL 16508/0042), 10 mg (PL 16508/0043), 20 mg (PL 16508/0044), powder for solution for injection, and Mitomycin-C Kyowa 40 mg (PL 16508/0045), powder for intravesical solution.
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M & A Pharmachem is recalling specific batches as a precautionary measure, because a small number of pots from some batches have been found to contain discoloured tablets due to fungal contamination
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List of field safety notices (FSNs) from medical device manufacturers from 28 October to 1 November 2019.
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Manufactured by Philips 鈥� due to a software or hardware issue the device may fail to start or deliver defibrillation therapy.
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Class 2 Medicines Recall: Nutriflex Omega Plus 1250ml, 1875ml and 2500ml, PL 03551/0119, and Nutriflex Omega Special 625ml, 1250ml, 1875ml and 2500ml, PL 03551/0118 and Supplemented Product codes ASNSPOMCA, ASNSPOMSVA, ASNPLOMCA, ASNPLOMSVA (625ml, 1250ml, 1875ml 2500ml) (EL(19)A/31)
B Braun is initiating a recall of certain batches of the above products as a precautionary measure. This is because ongoing product monitoring has identified that some bags may not comply with the required specification thro鈥�
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List of field safety notices (FSNs) from medical device manufacturers from 21 October to 25 October
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Biogen Idec UK is recalling batches as a precautionary measure due to a manufacturing issue.
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Omega Pharma Limited and Galpharm International Limited are recalling unexpired stock from pharmacies and retail stores as a precautionary measure due to possible contamination with an impurity.
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Rosemont Pharmaceuticals Limited is recalling unexpired stock from pharmacies as a precautionary measure due to possible contamination with an impurity.
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Pfizer Ltd is recalling certain batches of Sayana Press for subcutaneous injection.
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Pfizer UK Limited is recalling batches as routine stability testing has identified that levels of a known impurity, 10-oxo-docetaxel, may exceed the acceptable level at end of shelf-life.
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List of field safety notices (FSNs) from medical device manufacturers from 14 October to 18 October
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Teva UK Limited trading as ratiopharm GmbH is recalling all unexpired stock of Ranitidine Effervescent Tablets from pharmacies.
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Alliance Pharmaceuticals Ltd has informed the MHRA that there are possible side effects not reported on the Patient Information Leaflet.
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Aventis Pharma Limited t/a Sanofi has informed the MHRA that a change to the Patient Information Leaflet concerning possible side effects for Rifadin (rifampicin) 150mg Capsules has not been implemented by the required timel鈥�
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List of field safety notices (FSNs) from medical device manufacturers from 7 October to 11 October
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Manufactured by Baxter 鈥� Communication error alarms may result in unintentional delay and interruption of treatment due to system shutdown.
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Manufactured by Ecolab/Microtek Medical Malta Ltd 鈥� bacterial contamination may cause an infection in patients.
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GlaxoSmithKline, trading as Glaxo Welcome Ltd, is recalling all unexpired stock of Zantac (ranitidine hydrochloride) prescription only medicines (POM) from pharmacies.
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Manufactured by Intersurgical 鈥� leaks or disconnection can result in insufficient oxygenation requiring medical intervention to avoid severe injury.
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List of field safety notices (FSNs) from medical device manufacturers from 30 September to 04 October
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The MHRA has notified Bausch and Lomb UK Limited of reports that Emerade pens have failed to activate. The MHRA is advising that Emerade devices should not be recalled.
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Manufactured by Intersurgical, used in devices made by other companies: cracks in swivel elbow connectors may lead to prescribed ventilation not being delivered.
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List of field safety notices (FSNs) from medical device manufacturers from 23 to 27 September 2019.
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List of field safety notices (FSNs) from medical device manufacturers from 16 to 20 September 2019.
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Martindale Pharmaceuticals Limited is recalling the above batch due to an issue with homogeneity.
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List of field safety notices (FSNs) from medical device manufacturers from 09 to 13 September 2019.
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Manufactured by CME (a BD company) 鈥� function may be affected by fluid getting into the pump and building up over time because of specific cleaning and disinfection practices.
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Dr. Reddy's Laboratories (UK) Ltd is recalling the above batch due to the potential for small particles of Aripiprazole active material to be present which may affect the efficacy of the product.
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List of field safety notices (FSNs) from medical device manufacturers from 02 to 06 September 2019.
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List of field safety notices (FSNs) from medical device manufacturers from 27 to 30 August 2019.
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List of field safety notices (FSNs) from medical device manufacturers from 19 to 23 August 2019.
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Manufactured by Equipmed and other trading names (listed in the 鈥楳anufacturer contacts鈥� section), distributed in the UK by Naturastudios. Do not use affected devices as they have been manufactured to unknown standards and th鈥�
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List of field safety notices (FSNs) from medical device manufacturers from 5 to 9 August 2019
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List of field safety notices (FSNs) from medical device manufacturers from 29 July to 2 August 2019
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Accord-UK Ltd is recalling the above batches due to the potential for small particles of Aripiprazole active material to be present which may affect the efficacy of the product. No relevant product complaints or adverse reac鈥�
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Summary List of field safety notices (FSNs) from medical device manufacturers from 22 to 26 July 2019.
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Medicines have been taken out of the regulated medicines鈥� supply chain during distribution. The products have been parallel imported into the UK by Kosei Pharma, CST Pharma and Ordinant Medical Solutions from Italy and they 鈥�
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Manufactured by Defiteq International BV or GGT Holding BV 鈥� the safety and performance of these devices cannot be verified and their safe use can no longer be assured.
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Manufactured by Becton Dickinson (BD) 鈥� tubes may contain a hole or be damaged or deformed, potentially causing blood leakage and/or an inadequate blood-to-additive ratio leading to incorrect test results.
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Chanelle Medical is recalling the above batch because a small number of packs have been found to contain tablets which are stuck together, with mould observed on some tablets. The mould has been identified as a Penicillium s鈥�