Smiths Medical Recalls BCI Remote Alarm Cables Over Patient Risk
A series of medical devices that are designed to alert caregivers to a potential problem are being recalled because there’s a possibility that the alarm sounds would not be emitted properly. Smiths Medical announced the recall, which affects BCI Remote Alarm Cables used in conjunction with the 9004 Canocheck Capnography System. The device is used… read more
British Armed Forces Minister Relates DePuy ASR Experience
In Britain, an estimated 10,000 people have received the DePuy ASR metal on metal hip implant. According to a new report, one of those persons is an armed forces minister and former soldier who underwent a hip implant procedure back in 2006. Five years later, he claims that the development of a non-cancerous tumor in… read more
Eliminating Fires in Homes That Contain Medical Oxygen
A number of people across the country use medical oxygen in their home, but having such a medical device on hand also poses a number of risks that consumers must plan for. When medical oxygen is on hand, the threat of a fire is far more apparent, as the overabundance of oxygen could cause a… read more
Air Embolism Risk Leads to Recall of Guardian II Hemostasis Valves
The potential threat of an air embolism has prompted Vascular Solutions to announce the recall of Guardian II NC and Guardian II Hemostasis Valves available between February of last year and this past February. The recall encompasses four separate model numbers: 8215, 8216, 8210, and 8211. These particular models could suffer from a defect that… read more
Chicago Jury Hears From DePuy President at All-Metal Hip Implant Trial
Two weeks have passed since the $8.3 million decision handed down by a jury for a plaintiff that brought a lawsuit against DePuy and Johnson & Johnson. Panish | Shea | Ravipudi LLP was deeply involved in those proceedings, which stemmed from allegations surrounding the DePuy ASR metal on metal hip implant. Although the plaintiff… read more
Da Vinci Surgical System Adverse Event Reports Prompt FDA Inquiry
The Food and Drug Administration is currently looking into whether or not a device meant to aid in a surgeon’s ability to safely conduct procedures instead poses a risk to patients. In doing, the agency hopes to establish whether or not user error or a problem with the device itself could be to blame for… read more
DePuy ASR Designer Questioned During Trial
One of the surgeons responsible for the design of the DePuy ASR metal on metal hip implant has testified at a trial currently going on in Los Angeles at the state court level. His testimony reveals some startling information about the way complaints are reported and the failure rates that even experienced medical professionals could… read more
Justice Department Investigates Alleged J & J False Product Claims
Johnson and Johnson is currently the target of more than 10,000 lawsuits in regards to the company’s DePuy ASR metal on metal hip implant. Now, a report shows that the government actually initiated an investigation into the company last year in order to determine whether or not officials made false claims to federal healthcare programs…. read more
Taking Steps to Ensure Medical Device Safety Amid Severe Weather
Large swaths of the country are hunkering down in preparation for a winter snow storm, and those persons most in danger during such emergencies are those who rely on medical devices for their safety and health. The Food and Drug Administration wants to hear from the public and from medical professionals about how the ongoing… read more
FDA Explains The Risks of Breast Implants
The Food and Drug Administration is attempting to explain to consumers the risks of breast implants. Concerned that many people out there are overwhelmed when it comes time to research the implants, the FDA hopes to provide various resources that one can consult in order to ensure their safety if they undergo an implant procedure. … read more
Infant Warmer Component Recalled By GE Over Possible Health Risk
A component that could be found within Panda and Giraffe infant warmers is being recalled by GE Healthcare. The recall pertains to the field upgrade kit for resuscitation systems with blender. Each of the affected upgrade kits would have been produced between April 2008 and September of last year. Owners began receiving notices as early… read more
FDA Advises Safety When Undergoing a Tattoo Removal Procedure
Are you one of the many consumers who has gotten a tattoo, perhaps during a particularly wild night of partying, only to regret doing so either immediately or at some point down the line? If so, you’re not alone. Of the more than one in five people who have gotten some kind of tattoo, 14%… read more