Toyota (Gb) Avensis and Verso recall: Loss of power
Internal cluctch pistons may have been incorrectly manufacturerd. This may cause incorrect transmission operation.
Every new product, food, vehicle, medicine and pet recall in the UK, newest first. Checked against official sources every 15 minutes. 10,759 listed.
Internal cluctch pistons may have been incorrectly manufacturerd. This may cause incorrect transmission operation.
On affected vehicles the bolts retaining wall mounted seat belts and grab handles may not conform to specifications. These bolts could become loose and affect the security of the seat belt and grab handle.
The high-voltage battery charger may not have been produced to specification which could lead to an incorrect detection of an external charging cable. This in turn can lead the request for �P� to be…
A manufacturing defect of a component within any of the four door locks could result in jamming of the internal mechanism which prevents the closing of any of the vehicle's doors or risk unexpected…
A manufacturing defect of a component within any of the four door locks could result in jamming of the internal mechanism which prevents the closing of any of the vehicle's doors or risk unexpected…
Specific batch manufactured by Syner-Medica Ltd is being recalled due to concerns it may go out of specification for potency before it expires.
Teva UK Limited is recalling 2 batches as a precautionary measure after visible particles were found during testing.
Specific batch distributed by Sandoz Ltd is being recalled due to particulate matter found in samples.
(Zentiva) Pharmacists should quarantine remaining stock and return to original wholesaler (EL (15)A/13)
(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…
Hospira UK Limited is recalling 2 specific batches after atypical results for impurities were identified during routine testing.
Accord Healthcare Limited is recalling a specific batch which has inadvertently been distributed in the UK, because it is labelled for the Portuguese market.
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.
Based on MHRA’s review of available data, the Commission on Human Medicines’ Paediatric Medicine Expert Advisory Group (PMEAG) has advised that Wockhardt UK’s Amoxicillin Sodium Powder for Solution for Injection can be used with…
(Laboratoire SERB) EAN barcode is incorrect – when scanned, it identifies the product as Primidone SERB 250mg tablets not 50mg tablets (EL (15)A/10)
(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)
Ferring Pharmaceuticals Limited is recalling all batches of Bravelle 75IU powder for solution for injection on the UK market.
(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).
Recalls of medicines issued by manufacturers.
Beecham Group plc trading as GlaxoSmithKline UK is recalling specific batches of Bactroban 2% Nasal Ointment 3g and Bactroban 2% Cream 15g.
(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).
Recalls of medicines issued by manufacturers.
(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/06).
(CooperSurgical under different brand names) Risk of serious burn if device is used past its expiry date (MDA/2015/025)