Lawmakers in Ohio have tentatively passed new regulations governing hydraulic fracturing (fracking) drilling but they’ve immediately been criticized for being too favorable to the natural gas and oil industries.
The manufacturer of Plavix continues to be named in lawsuits alleging the blood thinner caused some patients to suffer from serious bleeding side effects. Most recently, the national law firm of Parker Waichman LLP filed nine Plavix bleeding lawsuits in state court in New York.
An emerging report reveals that older hip implant and knee replacement patients face increased heart attack risks following surgery. The risk for acute myocardial infarction (AMI) was seen in the first two weeks after these surgical procedures.
Regulators in the U.K. are once again issuing advice to doctors and other healthcare professionals involved in the follow-up of patients with metal-on-metal hip replacement devices. In an alert issued by the Medicines and Healthcare products Regulatory Agency (MHRA), guidance is provided for four groups of metal-on-metal hip implant ...
Wright Medical Inc. took steps in to 2006 to convince the U.S. Food & Drug Administration (FDA) to reject pre-market approval of rival Smith & Nephew’s Birmingham metal-on-metal hip implant. Wright Medical, which makes two metal-on-metal hip replacement devices, the Conserve and the Lieneage device, filed a citizen petition ...
Federal regulators have deemed CooperVision Inc.’s expanded Avaira Sphere contact lens recall a Class I recall, according to an announcement from the U.S. Food & Drug Administration (FDA). The expanded recall, which was announced on November 15, involved CooperVision’s Avaira … Continue reading →
CooperVision Inc. is expanding its recent contact lens recall to include to an additional brand. With the expansion, the < "http://www.yourlawyer.com/topics/overview/coopervision-avaira-topic-contact-lens-recall-eye-injury-lawyers">CooperVision contact lens recall now includes an additional 6 million lenses sold under the Avaira Sphere brand name. In October, … Continue reading →
CooperVision Inc.’s recent recall of Avaira Toric contact lenses has been deemed Class 1 by the U.S. Food & Drug Administration (FDA). Class 1 recalls are the FDAâ€™s most serious type of recall, and means the agency has determined there … Continue reading →
Pressure from U.S health regulators finally prompted CooperVision Inc. to step up its efforts to get the word out about its recent < "http://www.yourlawyer.com/topics/overview/coopervision-avaira-topic-contact-lens-recall-eye-injury-lawyers">recall of Avaira Toric contact lenses. According to a report from MSNBC, CooperVision is also acknowledging that … Continue reading →
While contact lens wears were suffering from blurry vision and agonizing pain that, in some cases, led to emergency room hospital visits, CooperVision was recalling < "http://www.yourlawyer.com/topics/overview/coopervision-avaira-topic-contact-lens-recall-eye-injury-lawyers">Avaira Toric contact lenses in what one popular blogger described as a â€œstealth recall.â€ … Continue reading →