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Dr. Richard Berger, a Chicago surgeon who was a long time user of Zimmer implants, has urged the manufacturer to recall some of its artificial knee implants, reports the New York Times.

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Dr. Berger was a long-time consultant to Zimmer on its products. He began experiencing premature failure of the Zimmer NexGen CR-Flex Porous Femoral knee replacement. A 2010 study indicates that the failure rate after only a few years may be as high as 9%. The study reveals that 36% of patients implanted with the Zimmer NexGen CR-Flex Porous show signs of implant loosening after only 2 years.

Zimmer has responded by criticizing Dr. Berger’s surgical technique, which is interesting, because over the years Zimmer has paid Dr. Berger almost $8 million to lecture and train surgeons in how to use and implant this and other Zimmer products.

To date, Zimmer has refused to order a recall. However, litigation is underway against Zimmer for these high failure rates. If you have a Zimmer knee implant and have experienced knee stiffness, knee pain, diminished motion in the joint, difficulty with weight bearing, have been told that your implant is loose or that you need a revision, you may have a claim against Zimmer for this defective product.

Contact Todd N. Hendrickson at HendricksonLaw.com or 314-721-8833 or toll free at 1-800-557-8176 for a free consultation.

Target has issued a recall on certain models of its Circo and Do Your Room brand step stools. These step stools with built in storage were sold for $25 to $30 between 2007 and 2010.

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Bloomberg News reports that there have been 27 reports of the stools breaking or collapsing and 14 reports of injuries.

If you have been injured as a result of the Target Circo and Do Your Room brand step stools or any other defective product, call or contact Todd N. Hendrickson and Hendrickson Law for a free consultation. You may be entitled to compensation for your injuries.

Have you or a family member contracted a serious infection following a procedure at a hospital or doctor’s office that involved prepping the site with an alcohol wipe? If so, you may have a legal case against the manufacturer of the wipe.

A truly massive recakk of Triad Alcohol Prep Pads has been issued. The original recall in January 2011 was rather limited, however, as months have gone by, the recall has grown. Triad Alcohol Prep Pads, Alcohol Swabs can be identified by the manufacturer Triad Group. They have also manufactured these products for sale by companies such as Walgreens, CVS, Smith & Nephew, GlaxoSmithKline, Eli Lilly and others. These products may be contained in various “kits” used by nurses and doctors, such as IV prep, blood draw and procedure kits.

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The Triad products were contaminated with Bacilus cereus, a bacteria that is normally soil dwelling. Normal symptoms of Bacilus cereus infection would include diarrhea, nausea and vomiting. At least one death has been linked to these contaminated products.

If you suspect that you or a family member was infected with Bacilus cereuas and you suspect it was caused by use of a contaminated alcohol prep, please contact the Law Offices of Todd N. Hendrickson, P.C. at www.hendricksonlaw.com.

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Almost 100,000 patients have received the DePuy ASR, metal-on-metal hip implant system. Those implants are failing at an alarming rate, at least 13% in the first few years. That is far beyond any “normal” failure rate. As a result, DePuy, a subsidiary of Johnson & Johnson, has recalled these hips.

The problem is, you can’t easily “recall” medical devices that have been implanted. That means they have to be explanted, or surgically removed and replaced. In the case of hip implants, this is called a revision, and it can be an expensive and painful operation.

If you have a DePuy ASR metal-on-metal hip implant, and you talk to your doctor about a hip revision, please talk to an attorney before you have the surgery. Reports are appearing around the country of hospitals treating these explanted hip components as medical waste and discarding them. Don’t let them do this to you! The removed implant is vital evidence. Just because the hip has been recalled doesn’t mean that you will automatically win a case against DePuy. You will still have to prove that the implant was defective in some way and the implant itself is the best evidence.

Please contact our office you have had a DePuy hip implant and need to discuss your legal rights.