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List of field safety notices (FSNs) from medical device manufacturers from 29 February to 4 March 2016.
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CME has recommended the need for protection of these pumps when exposed to direct sunlight.
In addition, due to connector leakages, the manufacturer is recalling extension sets (specific product codes and batches) used with…
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AMCo are recalling the listed batches of Maxolon 5mg/ml as the outer carton contains incorrect administration instructions.
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List of field safety notices (FSNs) from medical device manufacturers from 22 February to 26 February 2016
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List of field safety notices (FSNs) from medical device manufacturers from 15 February to 19 February 2016
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List of field safety notices (FSNs) from medical device manufacturers from 8 February to 12 February 2016.
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List of field safety notices (FSNs) from medical device manufacturers from 1 February to 5 February 2016.
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Action within 48 hours: patient, pharmacy and retail level recall of St John's Wort tablets. Testing has shown the presence of a toxic pyrrolizidine alkaloid (PA) above the threshold recommended by the Committee on Herb…
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List of field safety notices (FSNs) from medical device manufacturers from 25 January to 29 January 2016.
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Precautionary recall because a glass particle has been identified in one syringe from this batch.
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List of field safety notices (FSNs) from medical device manufacturers from 18 January to 22 January 2016.
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List of field safety notices (FSNs) from medical device manufacturers from 11 January to 15 January 2016.
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List of field safety notices (FSNs) from medical device manufacturers from 4 January to 8 January 2016.
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List of field safety notices (FSNs) from medical device manufacturers from 28 December to 1 January 2016.
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List of field safety notices (FSNs) from medical device manufacturers from 21 to 25 December 2015
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Specific batch manufactured by Syner-Medica Ltd is being recalled due to concerns it may go out of specification for potency before it expires.
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List of field safety notices (FSNs) from medical device manufacturers from 14 to 18 December 2015
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Specific batch distributed by Sandoz Ltd is being recalled due to particulate matter found in samples.
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Teva UK Limited is recalling 2 batches as a precautionary measure after visible particles were found during testing.
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A list of all medical device alerts that were archived in December 2015.
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(Zentiva) Pharmacists should quarantine remaining stock and return to original wholesaler (EL (15)A/13)
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List of field safety notices (FSNs) from medical device manufacturers from 7 to 11 December 2015
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Manufactured by Medtronic – battery voltage may reduce to a point where the device is no longer able to provide patient pacing therapy - MDA/2015/038
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(Pfizer Limited) Defect found to create the possibility of the dose being set to one extra click beyond the dose selected and indicated in the memory window when the patient turns the dose knob with excessive force (EL (15)A…
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List of field safety notices (FSNs) from medical device manufacturers from 30 November to 4 December 2015
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Hospira UK Limited is recalling 2 specific batches after atypical results for impurities were identified during routine testing.
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Accord Healthcare Limited is recalling a specific batch which has inadvertently been distributed in the UK, because it is labelled for the Portuguese market.
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List of field safety notices (FSNs) from medical device manufacturers from 23 to 27 November 2015
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Baxter is recalling a batch of Cernevit powder for solution for injection or infusion as a precautionary measure after receiving 2 complaints of glass particles in vials.
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List of field safety notices (FSNs) from medical device manufacturers from 16 to 20 November 2015
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List of field safety notices (FSNs) from medical device manufacturers from 9 to 13 November 2015.
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(Laboratoire SERB) EAN barcode is incorrect – when scanned, it identifies the product as Primidone SERB 250mg tablets not 50mg tablets (EL (15)A/10)
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List of field safety notices (FSNs) from medical device manufacturers from 2 to 6 November 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 26 to 30 October 2015.
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(AstraZeneca UK Limited) This presentation cannot be administered by intra-articular means as it states on the carton and ampoule label on all batches released since December 2012 (EL(15)A/09)
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List of field safety notices (FSNs) from medical device manufacturers from 19 to 23 October 2015.
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Ferring Pharmaceuticals Limited is recalling all batches of Bravelle 75IU powder for solution for injection on the UK market.
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List of field safety notices (FSNs) from medical device manufacturers from 12 to 16 October 2015.
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Manufactured by Coloplast A/S – temporary suspension of the CE certificate due to particles found on some implantable devices made by their subcontractor Silimed lndustria de lmplantes Ltda - MDA/2015/036
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List of field safety notices (FSNs) from medical device manufacturers from 5 to 9 October 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 28 September to 2 October 2015.
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A list of all medical device alerts that were archived in September 2015.
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Suspension due to particles found on some devices (MDA/2015/034)
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List of field safety notices (FSNs) from medical device manufacturers from 21 to 25 September 2015.
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(Allergan Limited) Small number of complaints have been received about small black particles found on or around the nozzle of the tube (EL (15)A/08).
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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 14 to 18 September 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 7 to 11 September 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 31 August to 4 September 2015.
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List of field safety notices (FSNs) from medical device manufacturers from 24 to 28 August 2015.