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Recordati Rare Diseases T/A Recordati Rare Diseases UK Ltd has made the MHRA aware that specific batches of Pedea 5 mg/ml solution for injection have been packaged with the incorrect Product Information Leaflet (PIL).
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List of Field Safety Notices (FSNs) from 17 to 21 October 2022
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Sanofi UK is initiating an urgent recall of two batches of Targocid 200mg powder for solution for injection/infusion or oral solution
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hameln pharma ltd is initiating a recall of the affected batches of Ephedrine Hydrochloride 30 mg/ml Solution for Injection as a precautionary measure.
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List of Field Safety Notices (FSNs) from 10 to 14 October 2022
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List of field safety notices (FSNs) from medical device manufacturers from 23 to 27 December 2019.
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Flamingo Pharma UK Ltd has identified an error relating to the ink printing of the batch number and expiry date on the carton for three batches of Ibuprofen 400mg Tablets. This notification includes all potentially impacted …
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List of field safety notices (FSNs) from medical device manufacturers from 04 to 08 October 2021
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hameln pharma ltd is initiating a recall of batch 210505 of Amiodarone Hydrochloride 50 mg/ml Concentrate for Solution for Injection/Infusion as a precautionary measure
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Summary list of field safety notices (FSNs) from medical device manufacturers from 24 August to 28 August 2020.
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List of field safety notices for week 03 to 07 October 2022
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Sanofi is recalling all batches of Stemetil 5mg/5ml Syrup as a precautionary measure due to the identification of N-nitrosomethylphenylamine (NMPA) above the acceptable limit.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 26 to 30 September 2022.
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Summary List of field safety notices (FSNs) from medical device manufacturers from `9 to 23 September 2022.
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Venous and arterial pressure limits may be altered unintentionally following acknowledgement of the alarm in some haemodialysis and haemofiltration machines. If the cause of the alarm is not addressed, the machine may not re…
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Summary List of field safety notices (FSNs) from medical device manufacturers from 12 to 16 September 2022
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Novartis Pharmaceuticals UK are recalling a batch of Sandimmun Oral Solution due to the presence of crystals in the solution.
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Rosemont Pharmaceuticals Ltd. has made the MHRA aware that the expiry dates stamped on the base of the bottle are incorrect for 2 batches of Atorvastatin 4mg/ml Oral Suspension and 2 batches of Sildenafil 10mg/ml Oral Suspen…
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Summary List of field safety notices (FSNs) from medical device manufacturers from 5 to 9 September 2022
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Quadrant Pharmaceuticals Limited have informed the MHRA of an error with the Patient Information Leaflets (PILs) that have been packaged in various parallel imported batches.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 29 August to 2 September 2022.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 22 to 26 August 2022
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Hikma Pharmaceuticals USA Inc are recalling the below batches due to an out of specification result with related substances during testing for retain samples.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 15 to 19 August 2022.
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The UK Marketing Authorisation Holder has confirmed that a batch of Dysport 500 Units Powder for Solution for Injection is falsified and has been supplied by unauthorised distributors to the UK.
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Accord Healthcare have informed us of an error with the patient information leaflets (PILs) that have been packaged in some Rosuvastatin products.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 8 to 12 August 2022.
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List of field safety notices (FSNs) from medical device manufacturers from 11 to 15 October 2021
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Sun Pharmaceuticals are recalling batches of zoledronic acid due to out of specification results observed for Particulate Matter Test during routine stability testing.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 1 to 5 August 2022.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 11 to 15 July 2022.
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Stockport Pharmaceuticals are recalling a batch of Sodium Chloride Eye Drops 5% w/v as the sterile eye droppers supplied with the medicinal product have expired (January 2022).
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Clinigen Healthcare Ltd is initiating a recall of three batches of Mexiletine hydrochloride hard capsules due to a potential risk of underdose or overdose, which could have consequences for the safety of patients.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 25 to 29 July 2022.
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Philips Health Systems have identified an important safety issue due to potential unexpected shutdowns of all of their V60 and V60 Plus non-invasive ventilators. All V680 invasive ventilators used in critical care settings …
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List of field safety notices (FSNs) from medical device manufacturers from 18 to 22 July 2022.
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Novo Nordisk Limited would like to notify you of a defect that affects specific batches of NovoRapid FlexTouch prefilled pen device and batches of Saxenda FlexTouch prefilled pen device in the UK.
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Omega Pharma Limited have identified an error relating to the product packaging.
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hameln pharma ltd is initiating a recall of batch 207506 of Amiodarone Hydrochloride 50 mg/ml Concentrate for Solution for Injection/Infusion as a precautionary measure.
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Thornton & Ross have identified that the product labelling for some batches of ‘Pharmacy’ medicines do not contain the ‘P’ symbol, due to a packaging error on the bottle.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 4 to 8 July 2022.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 27 June to 1 July 2022
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Summary List of field safety notices (FSNs) from medical device manufacturers from 20 to 24 June 2022
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A.Vogel Ltd is recalling a specific batch of Pharmacy only medicine due to a small number of packs that were inadvertently supplied to non-pharmacy retail outlets.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 13 to 17 June 2022
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Altan Pharma Limited have identified an error relating to the product packaging. The incorrect concentration of phenylephrine base is provided on the overwrapping bag label.
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PCCA Limited have been made aware of an issue with the appearance of Ketamine 50mg in 5ml Oral Solution and Ketamine 100mg in 5ml Oral Solution.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 6 to 10 June 2022
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Bristol Laboratories Limited are recalling a batch of this product as a precautionary measure due to low dissolution test results reported during ongoing stability studies.
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Summary List of field safety notices (FSNs) from medical device manufacturers from 30 May to 3 June 2022.