Personal Injury and Wrongful Death

July 2005 FDA Recalls

PritzkerOlsen, P.A.focuses its practice on getting justice for people who have been injured. Every month the FDA issues recalls of dangerous and defective products. These products can cause serious injury or death. If you have or had a Guidant pacemaker or have been harmed by a Baxter infusion pump, we have the experience in defective medical devise litigation to help you get compensation for your injuries, including pain and suffering. Our Senior Partner, Attorney Fred Pritzker has had more than 30 years of experience. His food poisoning cases, including cases involving Listeria and Salmonella, have given him a national reputation in foodborne illness litigation. He has been recognized, once again, by his peers as a Super Lawyer and has been selected for inclusion in the current edition of The Best Lawyers in America.

Contact us regarding the following recalls or any other dangerous or defective products. You can reach us toll-free at 1-888-377-8900, email us at info@pritzkerlaw.com, or submit your situation for review by our legal counsel with our online form. Consultations are free, and your information is kept strictly confidential.

Golden Taste Salmon Salad Recalled Due to Potential Listeria Contamination

July 7, 2005 -- Golden Taste, Inc., Spring Valley, New York is recalling its Golden Taste Baked Salmon Salad in 7.5 oz. and 3.5 oz. and 5 lb. plastic containers because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Listeria infection can cause miscarriages and stillbirths among pregnant women. The recalled Golden Taste Baked Salmon Salad was distributed to retail stores throughout New York State & New Jersey.

Learn more about recall of Golden Taste Salmon Salad and possible Listeria risk.

Some Boxes of Vanilla Crème Oreos® May Contain Peanut Butter Filling

July 15, 2005 -- Nabisco Foods, a Kraft Foods company of East Hanover, NJ, is recalling approximately 838,000 of the 7.5 oz. boxes of Pure Milk Chocolate Covered Oreo® Sandwich Cookies with the UPC product code number of 44000 01094 and “Best When Used By” dates through 05NOV05 because some boxes may contain cookies with peanut butter crème filling, rather than the vanilla crème filling depicted on the front label. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Learn more about recall of Pure Mild Chocolate Covered Oreo® Sandwich Cookies.

Golden Taste Lox Salad Recalled Due to Potential Listeria Contamination

July 15, 2005 -- Golden Taste, Inc., 45 S. Central Avenue, Spring Valley, New York 10977 is recalling its Golden Taste Nova Lox Salad in 7.5 oz. and 3.5 oz. and 5 lb. plastic containers because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Listeria infection can cause miscarriages and stillbirths among pregnant women.
Learn more about Golden Taste’s recall of Nova Lox Salad and potential Listeria contamination.

FDA Announces Class I Recall of Baxter Healthcare's Colleague Volumetric Infusion Pumps

July 21, 2005--The U.S. Food and Drug Administration (FDA) is announcing that Baxter Healthcare Corporation of Deerfield, Ill., has initiated a worldwide recall of all models of its Colleague Volumetric Infusion Pumps because they can shut down while delivering critical medication and fluids to patients. Baxter has received six reports of serious injury and three reports of death associated with this shut-down problem. The affected are: Models 2M8151, 2M8151R, 2M8161, 2M8161R, 2M8153, 2M8153R, 2M8163, and 2M8163R.

Learn more about recall of Baxter Healthcare’s Colleague Volumetric Infusion Pumps.

Guidant Pacemakers Recalled Due to Potentially Defective Seal

July 22, 2005--FDA Announces Guidant’s Class I Pacemaker recall. The U.S. Food and Drug Administration (FDA) is notifying health care providers and patients that Guidant Corporation is voluntarily recalling certain pacemakers. A seal within the devices can leak, allowing moisture to affect the electronic circuits. This defect can cause the pacemakers to fail to provide pacing or can cause a rapid heart rate. Other unexpected device behaviors are also possible. The problems may occur without warning and can lead to loss of consciousness, and possibly heart failure and death.
Learn more about recall of potentially defective Guidant pacemakers.


Free Case Consultation





Logos
 
Fred Pritzker on Comcast Newsmakers

Fred Pritzker on Twitter

Fred Pritzker is listed in The Best Lawyers in America

 
 

This is attorney advertising. Past results do not guarantee a similar outcome. The result of each case is determined by the specific facts and the applicable law.