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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)
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(GlaxoSmithKline) Check each vial for cracks by turning upside down and looking for chips, cracks or damage where base meets side wall. (EL (14)A/15)
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(Boston Scientific) Rapid battery depletion leads to risk of loss of therapy. (MDA/2014/039)
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(All manufacturers) Delays in acting on field safety notices can compromise patient safety (FSNs). (MDA/2014/037)
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(St Jude Medical) These defibrillators can delay or reduce the therapy that can be delivered by the ICD.(MDA/2014/035)
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(McNeil Products Limited) Remaining stocks of the above products should be quarantined - class 2 action within 48 hours. (EL (14)A/14)
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(Teva UK Limited) red precipitate found during stability testing under cold storage conditions - class 2 action within 48 hours. (EL (14)A/13)
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(ViroPharma SPRL) Pharmacists should quarantine batches and return them to original wholesaler for credit - class 2 action within 48 hours. (EL (14)A/12)
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(Wockhardt UK Ltd) Remaining stock from affected batches should be quarantined and returned to the original supplier for credit - class 2 action within 48 hours. (EL (14)A/11)
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(Penn Pharma, distributed in Quantum Pharmaceutical livery) May result in evaporation of aqueous component of product and increase in concentration of Midazolam. (EL (14)/A10)
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(All types, makes and models) Report cases in women who have breast implants or who have had them removed. (MDA/2014/027)
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(Wockhardt UK Ltd) Should not be used in neonates and infants under 1 year old until further notice. (EL (14)A/09)
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(Reckitt Benckiser Healthcare (UK) Limited) Remaining stock of batches should be quarantined and returned to original supplier for credit. - class 2 action within 48 hours. (EL (14)A/08)
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(Mylan on behalf of Strides Arcolab International Limited) Remaining stocks of affected batches should be quarantined - class 2 action within 48 hours. (EL (14)A/07)
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(ITH Pharma Ltd) Remaining stocks should be quarantined and returned to original supplier for credit - class 2 action within 48 hours. (EL (14)A/06)