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DePuy identified reasons for the failure of the hip replacement system as component loosening, component malalignment, infection, fracture of the bone, dislocation, metal sensitivity and pain. Additional complications from the hip replacement system may include increased metal ion levels in the blood, bone staining, necrosis, swelling, nerve ...
In the second trial, an Illinois jury returned a verdict in favor of DePuy in a lawsuit brought by a nurse who had sought $5 million in damages. [ 7 ] On June 14, 2012, Johnson & Johnson completed the acquisition of Synthes , which was integrated with the DePuy franchise to establish the DePuy Synthes Companies of Johnson & Johnson. [ 8 ]
D019644. MedlinePlus. 002975. [edit on Wikidata] Hip replacement is a surgical procedure in which the hip joint is replaced by a prosthetic implant, that is, a hip prosthesis. [1] Hip replacement surgery can be performed as a total replacement or a hemi/semi (half) replacement.
A multistate team of litigators helped to negotiate a settlement with medical technology firm Stryker Corp. on Friday. Stryker, a Fortune 500 company, had been faced with multidistrict as well as ...
In September 2020, Johnson & Johnson started its 60,000-person phase 3 adenovirus-based vaccine trial. [104] The trial was paused on October 12, 2020, because a volunteer became ill, [105] but the company said it found no evidence that the vaccine had caused the illness and announced on October 23, 2020, that it would resume the trial. [106] [107]
Metallosis. Metallosis is the medical condition involving deposition and build-up of metal debris in the soft tissues of the body. [1] Metallosis has been known to occur when metallic components in medical implants, specifically joint replacements, abrade against one another. [1] Metallosis has also been observed in some patients either ...
After Schaap's death, his estate and members of his family filed a lawsuit against three physicians and Lenox Hill Hospital, alleging that his death had been caused by medical malpractice. Specifically, they alleged that, for two years before his surgery, Schaap had been given a powerful medication called amiodarone to treat an irregular heartbeat
Recall information. FDA develops a strategy for each individual recall that sets forth how extensively it will check on a company's performance in recalling the product in question. For a Class I recall, for example, FDA would check to make sure that each defective product has been recalled or reconditioned. In contrast, for a Class III recall ...