Yesterday, April 29, 2010, the U.S. Consumer Product Safety Commission announced the recall of two crib models: Simplicity Cribs and Graco®-Branded Drop Side Cribs due to serious risks of suffocation and strangulation.
The CPSC has announced a major crib recall of all Simplicity full size cribs with tubular metal mattress support frames. This crib recall covers both fixed side and drop side cribs. These Simplicity Cribs have been pulled ...
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Note to Reader: The FDA classified the recall as a Class I recall, meaning that Stryker’s Custom Cranial Implant Kit could predictably cause serious harm or death.
If you or someone you know has been implanted with a Stryker cranial implant and is suffering side effects or injuries, an individual’s legal rights incur time limits, contact our law firm at once.
Stryker’s Custom Cranial Implant Kit is used during ...
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Note to Reader: The FDA classified the recall as a Class I recall, meaning that Stryker’s Custom Cranial Implant Kit could predictably cause serious harm or death.
If you or someone you know has been implanted with a Stryker cranial implant and is suffering side effects or injuries, an individual’s legal rights incur time limits, contact our law firm at once.
Stryker’s Custom Cranial Implant Kit is used during ...
continue reading...On 12 October 2009, hospital officials at the renowned Los Angeles Cedars-Sinai Medical Center reported that a serious hospital error caused over 200 stroke patients to receive eight times the normal dose of radiation during a CT procedure known as the CT brain perfusion scan.
If you or someone you know was overdosed with radiation, contact our law firm by calling 877-737-8525, or email using the form to the right to learn your legal rights. Your consultation ...
continue reading...Raptiva, a drug used for treating psoriasis, was pulled from the market on April 9, 2009.
The FDA has reported that Raptiva can cause the development of a condition called progressive multifocal leukoencephalopathy. This is a neurologic disease that can be fatal. Anyone currently using Raptiva should communicate with their physicians so they can begin tapering off the drug, as it will no longer be available after June 8, 2009. Physicians are not supposed to issue any new prescriptions.
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continue reading...Raptiva is an injectable drug used for the treatment of psoriasis. It has been discovered to cause a serious brain infection called progressive multifocal leukoencephalopathy, or PML. The FDA has confirmed at least three cases of patients who died from PML after using Raptiva more than three years. According to the National Institutes of Health, PML usually lasts for months, 80 percent die within the first six months, and those who survive can be left with severe neurological disabilities.
In October ...
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