Target Recalls Room Essentials 4-Drawer Dressers Due to Tip-Over and Entrapment Hazards

Target Recalls Room Essentials 4-Drawer Dressers Due to Tip-Over and Entrapment Hazards The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in death or injuries to children. Units: About 175,000 (in addition, about 3,000 units were sold in Canada) Description: This recall […]

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Invokana has been linked to amputations and ketoacidosis

Our Ohio product liability attorneys are currently taking on Invokana claims related to amputations and ketoacidosis, which have been linked to the drug. Invokana (canagliflozin) is a prescription drug used to treat type-2 diabetes.  It was approved by the FDA in 2013 and developed by Janssen Pharmaceuticals.  In May 2015, the FDA issued a safety […]

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Datascope Corp./MAQUET Recalls Intra-Aortic Balloon Pumps Due to False Blood Detection Alarm and Ingress of Fluid into the Intra-Aortic Balloon Pump

The FDA has identified this as a Class I recall, the most serious type of recall.  Use of these devices may cause serious injuries or death. Recalled Product(s): Datascope Corp./MAQUET Intra-Aortic Balloon Pump Model/Item Numbers: CS100i, CSO100, CS300 Lot Numbers: All Lots Manufactured July 1, 2003 to June 16, 2017 Manufacturing Dates: July 1, 2003 […]

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FDA is advising health care professionals and patients not to use any liquid product manufactured by PharmaTech LLC, Davie, Florida, due to Burkholderia cepacia contamination

Liquid Drug Products Manufactured by PharmaTech and Distributed by Rugby Laboratories and Possibly Other Companies: FDA Advisory – Not to Use FDA is advising health care professionals and patients not to use any liquid product manufactured by PharmaTech LLC, Davie, Florida, due to Burkholderia cepacia contamination and the potential for severe patient infection. Rugby Laboratories, […]

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Phenobarbital 15 mg Tablets, USP by C.O. Truxton: Recall – Labeling Error on Declared Strength

ISSUE: C.O. Truxton, Inc. is voluntarily recalling lot 70952A of Phenobarbital Tablets, USP, 15 mg, to the consumer/user level. The manufacturer received a confirmed customer complaint that a bottle labeled as phenobarbital 15 mg was found to contain phenobarbital 30 mg tablets. This mislabeled product could expose the consumer or their pet(s) to potential overdosing […]

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Polaris Recalls Sportsman 850 and 1000 All-Terrain Vehicles Due to Burn and Fire Hazards

If you have been burned by a Polaris Sportsman 850 or 1000 all-terrain vehicles (ATVs) please contact one of our injury attorneys today. Hazard: The right side panel heat shield can melt, posing burn and fire hazards to riders. In addition, in 2015 Sportsman 1000 ATVs, the exhaust springs can stretch and damage the exhaust […]

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Little Tikes™ 2-in-1 Snug ‘n Secure Pink Toddler Swings Injury Lawyer

Little Tikes Recalls Toddler Swings Due to Fall Hazard Hazard: The plastic seat can crack or break, posing a fall hazard. Units: About 540,000 Description: This recall involves Little Tikes 2-in-1 Snug’n Secure pink toddler swings. The swings have a pink T-shaped restraint in front with a Little Tikes logo. The swing is suspended by […]

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Comprehensive Reverse Shoulder by Zimmer Biomet: Class I Recall – High Fracture Rate

Comprehensive Reverse Shoulder by Zimmer Biomet: Class I Recall – High Fracture Rate ISSUE: Zimmer Biomet is recalling the Comprehensive Reverse Shoulder because these devices are fracturing at a higher rate than is stated in the labeling. Fractures may result in revision surgeries which could cause serious adverse health consequences such as permanent loss of […]

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