Category Archives: CooperVision Contact Lenses

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DeflateGate’s Effects Impact Legal Gambling & the Economy


The NFL has initiated a probe into the New England Patriots following allegations that the team intentionally used overly deflated footballs.

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Johnson & Johnson Facing More Metal-on-Metal Hip Implant Woes, as DePuy Pinnacle Complaints Rise

Having already spent around $3 billion on its DePuy Orthopaedics ASR hip implant recall, Johnson & Johnson is facing another potential debacle involving a metal-on-metal version of its Pinnacle Hip Replacement System. According to a report from Reuters, Johnson & Johnson and its DePuy unit already face some 1,600 metal-on-metal ...

National Law Firms Calls for More FDA Action on Actos Bladder Cancer Threat

A national law firm is not satisfied with the way the U.S. Food & Drug Administration (FDA) has handled warnings regarding Actos (pioglitazone) bladder cancer risks. In a statement published today, Parker Waichman LLP called on the FDA to compel Takeda Pharmaceuticals, the maker of the type 2 diabetes drug, ...

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Bisphosphonate Study Confirms Atypical Thigh Fracture Risk

New research has confirmed the link between bisphoshonates, such as Fosamax, and atypical femur fractures, a type of thigh fracture that occurs spontaneously, without any major leg injury. The study, published in the Archives of Internal Medicine, also found that the risk of atypical thigh fractures increases the longer a ...

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Metal-on-Metal Hip Implant Lawyer Takes Issue with Statements Made by DePuy Orthpaedics Official During FDA Meeting

An attorney with a national law firm that represents victims of alleged metal-on-metal hip implant injuries has expressed dismay at some statements made last week regarding the regulation of all-metal hip replacement devices by an official with DePuy Orthopaedics. According to Daniel Burke, Senior Litigation Counsel at Parker ...

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Actos, Avandia May Up Risk for Diabetic Macular Edema

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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FDA Metal-On-Metal Hip Replacement Investigation Is Flawed, Researchers Say

The U.S. Food & Drug Administration’s (FDA) metal-on-metal hip replacement investigation is flawed, according to researchers.

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Knee Replacement Patients Should Consider Nickel Allergies before Surgery

Individuals considering undergoing knee replacement surgery should ask their doctors to run a test to determine if they have a nickel allergy. Determining if a patient suffers from a nickel allergy will ensure the right knee implant is chosen for their surgery, and possibly save them from considerable pain and ...

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Zadroga Act Cancer Decision Expected This Week

The federal official tasked with determining what ailments should be covered by the federal Zadroga Act is expected to decide by Saturday if certain cancers will be eligible for compensation. The decision is being eagerly awaited by thousands of first responders who believe they developed cancer due to exposure ...

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CooperVision Avaira Sphere Contact Lens Recall Most Serious Type, FDA Says

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

Posted in CooperVision Contact Lenses, Defective Medical Devices |

CooperVision Adds 6 Million Avaira Sphere Lenses to Contact Lens Recall

CooperVision Inc. is expanding its recent contact lens recall to include to an additional brand. With the expansion, the < "">CooperVision contact lens recall now includes an additional 6 million lenses sold under the Avaira Sphere brand name. In October, … Continue reading

Posted in CooperVision Contact Lenses, Defective Medical Devices |

CooperVision Avaira Toric Contact Lens Recall Most Serious Type, FDA Says

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 FDA’s most serious type of recall, and means the agency has determined there … Continue reading

Posted in CooperVision Contact Lenses, Defective Medical Devices |

FDA Threat Prompts CooperVision to Reannounce Avaira Toric Contact Lens Recall

Pressure from U.S health regulators finally prompted CooperVision Inc. to step up its efforts to get the word out about its recent < "">recall of Avaira Toric contact lenses. According to a report from MSNBC, CooperVision is also acknowledging that … Continue reading

Posted in CooperVision Contact Lenses |

CooperVision Quietly Recalled Contact Lenses Amid Reports of Torn Corneas, Vision Problems

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 < "">Avaira Toric contact lenses in what one popular blogger described as a “stealth recall.” … Continue reading

Posted in CooperVision Contact Lenses |

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