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FDA LINKS
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U.S. Food and Drug Administration (FDA)
The FDA is responsible for protecting the public health by assuring the
safety, efficacy, and security of human and veterinary drugs, biological
products, medical devices, our nation’s food supply, cosmetics, and products
that emit radiation. The FDA is also responsible for advancing the public
health by helping to speed innovations that make medicines and foods more
effective, safer, and more affordable; and helping the public get the
accurate, science-based information they need to use medicines and foods to
improve their health ...
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FDA Updates Consumers on Guidant Corporation’s Implantable Defibrillators
To help patients and doctors take appropriate action pertaining to the health risks of certain defibrillators from Guidant, the
FDA has classified the devices into three categories, with class 1 being the most
serious, based on the probability that the device failure could lead to adverse health effects
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Guidant Initiates Worldwide Physician Communications Regarding Important Safety Information and Corrective Action about Implantable Cardiac Defibrillators
The FDA advices physicians to discontinue implants of certain defective Defibrillators after Guidant Corporation voluntarily alerts physicians about important safety information regarding certain devices ...
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FDA Preliminary Public Health Notification: Guidant VENTAK PRIZM® 2 DR and CONTAK RENEWAL® Implantable Cardioverter Defibrillators
The FDA offers new information and recommendations on steps to take concerning malfunctions occurring with Guidant’s PRIZM® 2 and CONTAK RENEWAL® implantable cardioverter defibrillator (ICD) devices
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HEALTH & CONSUMER INFORMATION
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U.S. Consumer Product Safety Commision
The U.S. Consumer Product Safety Commission is charged with protecting the public from unreasonable risks of serious injury or death from more than 15,000 types of consumer products under the agency's jurisdiction ...
- Recalls.gov
Too provide better service in alerting the American people to unsafe, hazardous or defective products, six federal agencies with vastly different jurisdictions have joined together to create www.recalls.gov -- a "one stop shop" for U.S. Government recalls ...
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ConsumerReports.org
Empowering consumers with information to allow
for a fair, just, and safe marketplace ...
NEWS LINKS
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As Many As 69 Pacemaker Models May Have Failed; Two Deaths and Dozens of
Product Failures Led to Recalls
Consumer Reports - July 26, 2005
... On July 22, the Food and Drug Administration classified Guidant's recall
as Class I, the most serious kind. As many as 69 pacemakers may have failed
according to Guidant. All the reported failures occurred in devices that had
been implanted in patients for at least 44 months.
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Guidant Says 28,000 Pacemakers May Need Replacement
Guidant Corp.
say doctors should consider replacing cardiac pacemakers implanted in the chests of 28,000 people worldwide
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Defibrillator industry accelerating the pace of change
Due to continuing pressure and demand by patients, doctors and the FDA,
Guidant and other defibrillator companies are increasingly releasing more information
sooner about the possible defects of the devices
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Guidant Issues Warning on 28,000 Pacemakers
Guidant Corp. on Monday warned physicians that replacements might be needed
for nine pacemaker models made between 1997 and 2000, of which some 28,000
remain implanted in patients worldwide
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Defibrillator recall sends patients scrambling
Nervous patients called their doctors Monday to have potentially faulty
implanted heart devices checked out after the company offered to replace
thousands of them because of flaws ...
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FDA Gives Highest Warning About Certain Guidant Defibrillators
The government says a malfunction in some of the Guidant Corporation
defibrillators recalled recently could cause serious injury or death
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Guidant defibrillators recalled
A series of failures in Guidant Corp. defibrillators that resulted in two
deaths prompted the company to issue warnings to doctors ...
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FDA halts expansion of network to monitor medical device safety
North Reading medical technology consulting firm, said data from more
hospitals might have led to earlier detection of problems with Guidant's
defibrillators
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Lawsuit claims faulty implanted defibrillator caused death
The lawsuit, filed Wednesday in Duval Circuit Court, claims Guidant, of
Indianapolis, was aware of problems with its defibrillators for about three
years, but ...
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FDA: Some Guidant Defibrillators Recalled
The FDA says Guidant Corp. is recalling certain implantable defibrillators
and cardiac resynchronization defibrillators
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New worry for heart patients as Guidant defibrillators are ...
The latest Guidant safety announcement affects the Contak Renewal 3 model,
Contak ... At least 74,900 defibrillators worldwide are now under a safety
warning, with ...
LEGAL LINKS
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Guidant Lawyers
Online website providing
information about the Guidant Defibrillator Recall, product information, how
defibrillators work, and an easy online lawsuit evaluation form.
If you have any questions about your legal rights, please contact us to speak
with one of our lawyers. Recognized among the most distinguished law firms in
the United States in the Martindale-Hubbell® Bar Register of Pre-eminent
Lawyers,â„¢ Janet, Jenner & Suggs, LLC has won record breaking verdicts and
settlements through its aggressive advocacy.
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