J&J has had a rough time of late with the J&J talcum-powder lawsuit in which victims argued the use of such powder was a strong cause for ovarian cancer. On top of that we have the ongoing cases for hip replacement products that have been pursued across the world for several years now.
A $1 billion (£813 million) fine was slapped on both J&J and its subsidiary, Depuy Orthopaedics, after a Texas jury found that the metal-on-metal Pinnacle hip implants were defectively designed, and that no warnings were given to consumers to highlight the risk.
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There is a reported risk with the use of non-recommended syringes in Alaris syringe pumps, manufactured by CareFusion.
The non-recommended syringes are reported to have a broken spring in the plunger which may cause unintended bolus (usually chewed up mass in the mouth) of medication.
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Teva U.K. Limited – a global pharmaceutical company – has recalled a batch of class 2 medicines due to a possible metal contamination.
The pharmaceutical company has recently made a precautionary batch recall for a ‘small number’ of Evacal D3 chewable tablets. The tablets are a calcium-vitamin D supplement used to treat a lack of calcium and vitamin D, predominantly in the elderly.
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With all this technology, you’d have thought that apps were advanced enough to detect health dangers. However, this unfortunately may not be the case for many smartphone health apps.
We as Group Action Lawyers represent victims for Medical Group Actions and Data Breach Group Actions, so this is right up our avenue of experience.
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Valproate Semisodium, better known as Depakote, has reportedly put more than 10,000 pregnant women at risk in France, and there are raising concerns that the same amount of women in the U.K. may also be affected by the epilepsy drug.
Our Group Action Lawyers are investigating the issues, and anyone affected here in the U.K. is free to come forward for confidential and no obligation advice.
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The Stockert 3T heater-coolers used during certain surgeries have been linked to a dangerous microorganism, Mycobacterium chimaera.
The manufacturers of the ‘deadly device’ have now issued advice in relation to managing and cleaning the device as part of ongoing investigations.
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Since its introduction into the market, the Medtronic infusion pump has been apparently overwhelmed with problems.
In recent years, problems that have been linked to the use of the pumps have reportedly caused dozens of deaths. As such, health authorities and the manufactures are in the process of taking appropriate action, and we’ll be looking in to whether there is any negligence here.
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Birmingham surgeon Dr. Angamuthu Arunkalaivanan performed hundreds of the pelvic floor surgeries using a mesh implant that the Trust he worked for had banned from using.
Dr. Arunkalaivanan seemingly ignored the Trust’s instructions and carried on inserting these mesh implants into hundreds of women despite the warnings from the National Institute for Health and Care Excellence (NICE) of incontinence and infection, and his own Trust’s policy on their use.
Some 200 patients who have undergone pelvic floor surgeries with Dr. Arunkalaivanan have been recalled to be checked. However, pelvic floor operations are so routine that it may be many more than 200 woman affected by the surgeons actions.
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A stern warning for all patients prescribed the blood-thinning drug Rivaroxaban; sold under the name of Xarelto, that’s available on the NHS:
Due to a battery issue, medical equipment like implantable cardioverter defibrillators (ICD) and cardiac resynchronisation therapy devices (CRT-D) have reportedly failed, leading to serious concerns for patient health.
It’s thought that around 350,000 devices worldwide have been implanted and potentially put patient health at risk.
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Recent reports indicate that individuals taking medication known as beta-blockers and calcium antagonists for a period of more than 90 days may be susceptible to mood disorders that require hospital treatment.
These medications – commonly used to control blood pressure – are said to be a possible cause for major depression and / or bipolar disorder, drawn from comparisons with patients controlling their high blood pressure with angiotensin receptor blockers (ARBs) instead.
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Teva UK Limited are one of the latest pharmaceutical manufacturers that have recalled a batch of their drugs.
The Nacrez 75 mg film-coated tablets have been recalled due to impurities found as part of their routine testing. The recall is said to be a precautionary measure taken by the company to ensure the safety of their customers.
However, as with any medicine recall, the dangers to human health are always something to closely monitor.
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