Defective front disk brakes and quick-release levers installed on 1.3 million bicycles in the US may pose a risk of injury to bicycle riders. An open quick release lever on the bicycle’s front wheel hub can come into contact with the front disc brake rotor causing the front wheel to come…
Articles Posted in product liability
After a less than 1% response rate to an initial recall and a fourth death by entrapement, the US Consumer Product Safety Commission and Bed Handles Inc are re-anouncing the recall of defective portable bed handles
The company Bed Handles Inc is re-announcing the recall of 3 models of their portable bed handles because they are defective and have caused the death of 4 people. These products are: Bedside Assistant, Model BA10W, Travel Handles Use, Model BA11W, Adjustable Bed Handle, Model AJ1. When attached to an adult bed without the use…
Companies are spending more on Product Liability Litigation
Product liability litigation is one of the only areas of litigation that companies spent more on in 2015. A recent article in Law 360 provides an overview of the BTI Litigation Outlook 2016 report by BTI Consulting Group and indicates that companies have been spending more on product liability litigation in…
9 attorneys from our New York Personal Injury Law Firm were included in the The Best Lawyers in America© 2016
Gair, Gair, Conason, Rubinowitz, Bloom, Hershenhorn, Steigman & Mackauf is proud to announce that 10 of their New York Personal Injury Lawyers were listed in The Best Lawyers in America© 2016. Marijo Adimey, Jeffrey B. Bloom, Seymour Boyers, Anthony H. Gair, Howard S. Hershenhorn, Stephen H. Mackauf, Ben B. Rubinowitz, Christopher Sallay and Richard M. Steigman were selected…
After Takata, ARC Automotive is is the second company to be investigated by US Safety regulators for defective airbags
The National Highway Traffic Safety Administration (NHTSA) just announced that they were probing another company for defective airbags. According to the document posted on the NHTSA website, ARC Automotive is being investigated for airbag inflator rupture following two reports of incidents during which two people were injured. A first incident of airbag…
51 reports of personal injuries and one death prompt the FDA to announce an urgent Class I Recall of Maquet’s Tiger Paw System II, a medical device used during heart surgery
A defective surgical staple used to close tissue in the left atrial appendage of the heart is being recalled by the FDA after reports that patients suffered personal injuries such as tissue tears and bleeding including a possible tear of the left atrial wall (top left chamber) during use of the…
Beech-Nut recalls Classics Stage 2 Sweet Potato & Chicken after a piece of glass was found in a jar of the product
Attention parents, some Beech-Nut products may potentially be dangerous for your children and should be returned to the manufacturer for a refund. After a consumer found a small piece of glass in a jar Beech-Nut Stage 2 Sweet potato & Chicken, the manufacturer issued a voluntary recall of the product. The recalled…
Hospira recalls Lactated Ringer’s Irrigation, 3000mL, a sterile solution for injection, because of potential mold contamination
Hopsira announced a voluntary product recall after reports from customers indicated that a lot of Lactated Ringer’s Irrigation, 3000mL may be contaminated with mold. Lactated Ringers Irrigation is a sterile, nonpyrogenic solution of electrolytes in water for injection, intended only for sterile irrigation, washing and rinsing purposes. Contaminated solution can be fatal if…
Tylenol manufacturer admitted selling metal contaminated drug and agreed to pay $25 million to resolve the case
McNeil Consumer Healthcare, a subsidiary of Johnson and Johnson agreed to pay $25 million for selling children medicine contaminated with metal. The case started in 2009 after a consumer complained that he found black specks in a bottle of Infants’Tylenol. After analysis it appeared that faulty manufacturing was to blame…
With the first product liability lawsuits being filed against duodenoscope manufacturers, it was diclosed today that the devices that led to the CRE outbreak at UCLA where not FDA approved
Patients and family of patients that have been infected by contaminated duodenoscopes at UCLA Hospital started to file product liability lawsuits against Olympus, the manufacturer of the medical devices. 18 year old Aaron Young was the first one to file his lawsuit. The high school student is still hospitalized and receiving treatment for …