Header image

CNN reports that a popular inflatable pool slide, sold by Wal-Mart and Toys R Us, has been recalled due to deaths and severe injuries.

The U.S. Consumer Product Safety Commission has order the recall of the Banzai Splash inflatable pool slide. The slide can partially deflate, causing serious injuries. At least one death and one incident of paralysis have been reported. Additionally, the slide is unstable and carries inadequate warnings and instructions.

120510073354-banzai-falls-slide-recall-story-top.jpg

If you or a family member has been injured as a result of using one of these slides, please call our office immediately for a consultation. You must act quickly to protect your rights. Contact us at 1-800-557-8176 or click here.

The New York Times has a recent article on The High Cost of Failing Artificial Hips that does a good job of outlining the the cost related to the seemingly epidemic failure of the metal-on-metal hip implants from DePuy and others. If you’ve had a hip replacement in the last 10 years, I would recommend that you read it here.

hip-replacement-220.jpg

If you have a DePuy ASR or Pinnacle metal-on-metal hip implant, I would strongly urge you to contact me to discuss your rights. Even if you are not currently experiencing problems with your hip replacement, you should be aware of the pending litigation and what you should do.

To be clear, there is no class action currently pending for these implants and I don’t anticipate that there will be. What is in place is called a Multi-District Litigation that has some of the characteristics of a class action, but differs in many ways. The most important difference is this: If you don’t file a lawsuit, your interests will not be protected and you will not receive a settlement. In the typical class-action anyone who can be identified as having received the defective product will receive notice of a settlement. That is not true in a Multi-District Litigation.

If you have had a DePuy ASR or Pinnicle, a Zimmer Duron or any other metal-on-metal implant, please contact me immediately at 1-800-557-8176 or see my website at www.stlmedicalmalpractice.com.

If your lovely Aunt Shelby give you a ShoulderFlex massager for Christmas … well, you don’t even want to re-gift this thing. And whatever you do, don’t use it!

shoulderflex_custom.jpg

The ShoulderFlex massager by now bankrupt King International was recalled in August. NPR reports that the FDA recalled the device because clothing, hair and jewelry can get tangled in the device’s rotating parts. There were reports of one person being strangled by the massager and at least one other near-death by strangulation.

Before the recall process could be completed, King International went into bankruptcy. The toll-free recall number has been disconnected. Many consumers who purchased the product may not have been advised of the recall.

If you own one, take it back to the store where you purchased it. After all, you don’t want to end up on one of those “news of the weird” shows.

Happy Holidays!

Medtronic medication pumps are widely used to deliver pain medication, anti-spasm medication and other prescriptions directly into the spinal cord. And the FDA has determined that these pumps can cause serious harm. The FDA has issued a Class 1 recall.

The SynchroMed II implantable pumps, models 8637-20 and 8637-40 are the subject of the recall which has been reported here. A Class 1 recall means that these pumps have a reasonable probability of causing serious adverse health consequences or death. The pumps are failing, apparently due to a defective design relating to the battery.

These pumps are surgically implanted under the skin with delivery tubes placed to the point of delivery. Medtronic is not recommending that the pumps be removed and replaced at this point, says MedPage Today.

If you or a loved one has experienced a failure related to one of these pain pumps, or if you have one of these pumps implanted, you should contact our office to discuss your legal rights. Contact us at 314-721-8833 or at www.stlmedicalmalpractice.com.

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.

ZIMMER-articleLarge.jpg

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.

Circo Step Stool.jpg

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.

The FDA has recalled Bard Surgical mesh distributed by RAM Medical, Inc., a medical product distributor in Wayne, New Jersey.

Surgical mesh is used in hernia and other abdominal surgeries to strengthen or repair defects in the abdominal wall or peritoneum. For example, in repairing an abdominal hernia, a surgeon may use surgical mesh to create a “backing” that will reinforce the repair.

The counterfeit Bard surgical mesh ranges in size from 2″x4″ to 10″x14″. It is not properly sterilized, the edges are not properly finished and the weave is larger. This mesh can cause infection and failures of the repair, necessitating additional surgeries and other complications. The counterfeit mesh was distributed beginning October 21, 2008. You can review the recall notice here.

If you or a loved one had a surgery using mesh after October 21, 2008, and have experienced any infection, pain or other complications, you may have received the recalled mesh. If so, you have legal rights that need to be protected. Please call the Law Office of Todd N. Hendrickson at 314-721-8833, or click here to submit an inquiry.

DePuy, a division of Johnson & Johnson, has issued a recall on its ASR hip replacement components, including the ASR Hip Resurfacing System and the ASR XL Acetabular System. You can read about the recall here.
The DePuy ASR components are known as metal-on-metal components. Rather than using a poly-vinyl, ceramic or other material pelvic cup surface, the DePuy, like many other manufacturers, designed the ASR system to utilize a metal ball head and metal pelvic cup. The result is apparently is a disaster.
By some reports, more than 13% of these implants are failing within five years. The average him implant lasts 15-20 years before it wears out and needs to be revised. The highest rate of failure is in the smaller ASR implant sizes, 50mm and less, the most common sizes implanted in women.
If you have an ASR hip implant that has been revised due to early loosening or other problems, please contact the office of Todd N. Hendrickson immediately. Our office is aggressively investigating these cases and can help you. It is important that you be represented by an experienced medical malpractice and medical product liability lawyer, as DePuy will attempt to defend these cases by claiming that surgeon error in implantation. Don’t trust your case to a so-called “mass tort” law firm that doesn’t prosecute medical malpractice cases.
Contact our office today, by clicking on this link.

Toyota has issued a massive recall as reported by USA Today and elsewhere. The recall affects:2009-2010 Rav42009-2010 Corolla2009-2010 Matrix2005-2010 Avalon2010 Highlander2007-2010 Tundra2008-2010 SequoiaCertain 2008-2010 Carolla modelsThe recall is due to reports that the gas pedal can stick, causing the driver to be unable to cease acceleration. A previous notice indicated that the problem was occurring due to the gas pedal sticking in floor mats, but this recall indicates that it can occur even when the floor mats have been removed.Toyota has taken the step of notifying its dealers to cease selling the current new models until the problem has been corrected. This recall affects millions of vehicles.If you have been involved in an accident in which you were driving one of these Toyota models, or were struck by one of these Toyota models, you may have a claim against Toyota for product liability, in addition to any other claim you may have. If you’ve been involved in an accident in any Toyota in which you know or suspect that it was caused due to a sticking accelerator, please contact The Law Offices of Todd N. Hendrickson immediately. You have rights and we are here to protect them. Please call at 314-721-8833 for a no cost consultation.