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Beecham Group plc trading as GlaxoSmithKline UK is recalling specific batches of Bactroban 2% Nasal Ointment 3g and Bactroban 2% Cream 15g.
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List of field safety notices (FSNs) from medical device manufacturers from 17 to 21 August 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 10 to 14 August 2015.
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A list of all medical device alerts that were archived in July 2015.
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(Teva UK Limited) 25mg has been incorrectly printed in one position of the affected foil packs however is correct in other positions (EL(15)A/07).
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List of field safety notices (FSNs) from medical device manufacturers from 3 to 7 August 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 27 to 31 July 2015.
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Recalls of medicines issued by manufacturers.
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List of field safety notices (FSNs) from medical device manufacturers from 20 to 24 July 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 13 to 17 July 2015.
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(Uab Norameda) distributor Peckforton Pharmaceuticals Limited has identified an error on the presentation of the 50ml carton - the coloured band on the package should be purple not pink although text is correct (EL(15)A/…
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List of field safety notices (FSNs) from medical device manufacturers from 6 to 13 July 2015.
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(CooperSurgical under different brand names) Risk of serious burn if device is used past its expiry date (MDA/2015/025)
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List of field safety notices (FSNs) from medical device manufacturers from 29 June to 3 July 2015.
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(Generics (UK) Limited, trading as Mylan UK) A small number of packs from a specific batch may have an over count or under count of one tablet (EL (15)A/05).
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List of field safety notices (FSNs) from medical device manufacturers from 22 to 26 June 2015.
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[Archived] (Smith & Nephew Orthopaedics) Birmingham Hip™ Resurfacing (BHR) system - higher than expected revision rate for certain patient groups (MDA/2015/024)
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List of field safety notices (FSNs) from medical device manufacturers from 15 to 19 June 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 8 to 12 June 2015.
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(All manufacturers) Low risk of Mycobacterium infection in patients undergoing cardiac surgery, associated with heater-coolers used with cardiopulmonary bypass machines. Possible cause may be Mycobacterium-contaminated water…
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A list of all medical device alerts that were archived in May 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 1 to 5 June 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 25 to 29 May 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 18 to 22 May 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 11 to 15 May 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 5 to 8 May 2015.
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(RelonChem Ltd/ Kent Pharmaceuticals) All unexpired batches of 50mg Tramadol capsules are being recalled due to the risk of fungal contamination. Class 2 – action within 48 hours. (EL (15)A/04)
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List of field safety notices (FSNs) from medical device manufacturers from 27 April to 1 May 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 20 to 24 April 2015.
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(Allergan UK Limited) Specific batch including a Danish language pack was shipped to the UK in error. Class 3 – action within 5 days. (EL (15)A/03)
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List of field safety notices (FSNs) from medical device manufacturers from 13 to 17 April 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 7 to 10 April 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 30 to 3 April 2015.
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Sanofi is recalling a specific batch of syringe barrels used in batch 4LL66 of this product, distributed from 12 January 2015.
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(Aventis Pharma Limited and Winthrop Pharmaceuticals UK Limited) The smell associated with some batches is said to be a result of the foil packaging, but patients should continue taking their medicine. (EL (15)A/02)
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List of field safety notices (FSNs) from medical device manufacturers from 23 to 27 March 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 16 to 20 March 2015.
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Takeda UK Ltd is recalling a specific batch of Vitaros 3mg/g cream 4 x 100mg.
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Takeda UK Ltd is recalling specific batches of Rienso 30mg/ml solution for infusion (Ferumoxytol).
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List of field safety notices (FSNs) from medical device manufacturers from 9 to 13 March 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 2 to 6 March 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 23 to 27 February 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 16 to 20 February 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 9 to 13 February 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 2 to 6 February 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 26 to 30 January 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 19 to 23 January 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 12 to 16 January 2015.
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(Novartis Consumer Health UK Limited and Actavis Group PTC EHF): Product reclassified from P to POM due to safety concerns – class 2 action within 48 hours (EL (15)A/01)
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(Lundbeck Limited) May result in suboptimal dosage of the product - class 2 action within 48 hours. (EL (14)A/19)