Product Liability Law Firm in MN
Pritzker Olsen Attorneys Product Liability Blog

Pritzker Olsen attorneys have appeared on CBS News, Fox news, and numerous local television stations throughout the country. They have recovered millions for people injured by defective products. To contact our law firm, please call 1-888-377-8900 (toll free) or submit our free consultation form.

Age Intervention Eyelash, Bimatoprost and Vision Problelms

If you have been using Age Intervention Eyelash and now have vision problems, you may have a claim against Jan Marini Skin Research, Inc., the the seller and distributor of Age Intervention Eyelash.

Today, at the request of the U.S. Food and Drug Administration, U.S. Marshals seized 12,682 applicator tubes of Age Intervention Eyelash for the following reasons:
  • FDA considers the seized Age Intervention Eyelash to be an adulterated cosmetic. The product contains bimatoprost, an active ingredient in an FDA-approved drug to treat elevated intraocular pressure (elevated pressure inside the eye). For patients using the prescription drug, using the Age Intervention Eyelash in addition to the drug may increase the risk of optic nerve damage because the extra dose of bimatoprost may decrease the prescription drug's effectiveness. Damage to the optic nerve may lead to decreased vision and possibly blindness. In addition, use of Age Intervention Eyelash may cause other adverse effects in certain people due to the bimatoprost, including macular edema (swelling of the retina) and uveitis (inflammation in the eye), which may lead to decreased vision.
  • FDA considers Age Intervention Eyelash to be an unapproved and misbranded drug because Jan Marini Skin Research has promoted the product to increase eyelash growth. Before a new drug product may be legally marketed, it must be shown to be safe and effective, and approved by FDA.
If you have been using Age Intervention Eyelash and now have vision problems, you need to consult your health care provider regarding the effect bimatoprost may have had on your vision. If you are diagnosed with macular edema, uveitis or any damage to the optic nerve, contact one of out product liability lawyers as soon as possible regarding a possible lawsuit against Jan Marini Skin Research and any other parties that may be responsible for your injuries. To contact us, please call toll-free at 1-888-377-8900 or submit the online consultation form on the upper-right-hand corner of this page.

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Aqua Dots Recall Prompted by Injuries to Children

A chemical coating on Aqua Dots converts to a powerful “date rape” drug when ingested. Two children in the United States slipped into a coma after swallowing some of the Aqua Dots. As a result Spin Master, manufacturer of Aqua Dots, has recalled 4.2 million Aqua Dot products, which were manufactured in (you guessed it) China.

Millions of toys sold in the U.S. and manufactured in China have been recalled due to high lead content (usually in the paint). Now Chinese manufacturers are coating products meant for children with a “date rape” drug. What will be next?

Legally, Spin Master is liable for any injuries to children that are caused by Aqua Dots. We are using “caused” in the legal sense, which means it has to be more probable than not that Aqua Dots caused a specific injury. We are accepting Aqua Dots lawsuit cases. If your child has been seriously injured by Aqua Dots, please contact us toll-free at 1-888-377-8900 or submit the online consultation form for review by one of our nationally-recognized product liability lawyers.

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Wendy Bellissimo Collection Convertible Cribs Recalled

Wendy Bellissimo Collection convertible cribs have been recalled due to possible entrapment and strangulation of infants. The cribs were made in China and sold by Bassettbaby, a Bassett, Virginia company.

The bolts connecting the top corners of the recalled cribs can come loose, creating a gap and posing a serious entrapment and strangulation hazard. Bassettbaby has 85 reports of bolts loosening, including one report of a 13 month-old child’s hand becoming entrapped between the railings.

The crib recall involves about 8,900 Wendy Bellissimo Collection convertible cribs, model numbers 5945-0521 and 5545-0521, sold in honey and cherry finishes. The full size cribs have a sleigh design and one of the following purchase order numbers at the bottom rail of the headboard: 272903, 272904, 273904, 276728, 276729, 291081, 323975, 324472, 320318, 323976, 332883 365620, 368466 in honey, and 338535, 338537 and 332884 in cherry. All other Wendy Bellissimo Collection cribs are not involved in this recall.

The recalled cribs were sold at Babies R Us stores nationwide from July 2005 through October 2007 for about $500. Consumers should stop using these cribs immediately and contact Bassettbaby for a free repair kit. If your infant has been injured by a recalled crib, contact an attorney immediately. We are accepting cases of serious injury associated with cribs, including Wendy Bellissimo Collection convertible cribs and Simplicity cribs.

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Pritzker Olsen attorneys have appeared on national television and have been quoted by national publications, including The New York Times, The Wall Street Journal, Associated Press and Lawyers USA. Attorneys Fred Pritzker, Elliot Olsen and Eric Hageman have been named "Super Lawyers" by Law and Politics magazine (2008 and previous years). Attorney Fred Pritzker is also listed in the current edition (2008) of The Best Lawyers in America. To contact Pritzker Olsen Attorneys, please call 1-888-377-8900 (toll free) or submit the firm's free consultation form.

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Yamaha Rhino Lawsuit

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Fred Pritzker Listed in The Best Lawyers in America

Fred Pritzker has been notified that he will again be listed in The Best Lawyers in America for his work in personal injury and wrongful death litigation.

 

Traumatic Brain Injury

Attorneys Fred Pritzker and Elliot Olsen spoke at the annual Minnesota Association for Justice Brain Injury Seminar. They represent brain injury survivors in product liability cases throughout the nation.

 

Medtronic Recall and Medtronic Lawsuit

FDA has annonced a Medtronic Spring Fidelis defibrillator lead recall. Two of our clients with defective Medtronic leads were shocked over twenty times before medical professionals were able to turn off the defibrillator.

 

Ortho Evra Lawsuit: Ortho Evra Birth Control Patch

The Ortho Evra birth control patch has been linked to an increased risk of blood clots that can lead to pulmonary embolism, stroke and heart attack.

 

Trasylol Recall

Bayer has agreed to a marketing suspension of Trasylol, a drug used to control bleeding during heart surgery, pending detailed review of preliminary results from a Canadian study that suggested an increased risk for death.

 

Fentanyl Lawsuit and Fentanyl Recall

There have been a number of recalls regarding fentanyl due to the risk of a fentanyl overdose.

 

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