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Arkansas 124 articles

Blood thinner recalled over drug ingredient mixup

International Laboratories LLC is recalling one lot of the blood thinner Clopidogrel because the pills may contain the cholesterol-lowering statin Simvastatin instead. The recall affects Lot # 117099A of Clopidogrel Tabloets, USP 75mg, packaged in bottles of 30 tablets. The affected lot was delivered to distribution centers in Arkansas, Georgia, Indiana, California and Maryland, and then distributed to retail stores throughout the U.S. Patients prescribed Clopidogrel, the active drug ingredient in Plavix, who miss doses of this medication are at an increased risk of heart attack and stroke, both of which can be life threatening. Additionally, unintentional consumption of Simvastatin, ... Read More

IberiaBank Whistleblowers Recover $11.7 Million For Taxpayers

A whistleblower lawsuit accusing IberiaBank of wrongfully certifying mortgage loans for federal insurance has led to an $11.7 million settlement, the U.S. Department of Justice (DOJ) announced. According to the Justice Department, two former IberiaBank employees, Kelley Shackleford and Karen Mills, filed the whistleblower complaint on behalf of the U.S. government under the whistleblower provisions of the False Claims Act (FCA). Both women formerly worked for IberiaBank in Little Rock, Arkansas. The whistleblower complaint alleged that the Lafayette, Louisiana-headquartered bank committed mortgage fraud by knowingly originating and underwriting federally insured mortgage loans that did not meet regulatory requirements. The agreement makes ... Read More

Kroger recalls infant water due to mold contamination

The Kroger Company is recalling Comforts FOR BABY Purified Water with Fluoride Added after receiving complaints that there was mold in the product. Laboratory testing identified the mold as Talaromyces penicillium, which can cause allergic reactions in some people. Affected products include 1 gallon (3.78 L) clear bottles with the sell by dates from April 26, 2018 to Oct. 10, 2018,  the UPC Code 0 41260 37597 2, and the plant code 51-4140. The labels also state DISTRIBUTED BY THE KROGER CO, CINCINNATI, OHIO 45202. The water was distributed to Kroger stores, including Food 4 Less, Jay C, Jay C ... Read More

3 Crew Dead After Medical Helicopter Crash in Arkansas

Three crew members were killed when their medical helicopter crashed Sunday night in DeWitt, Arkansas, approximately 60 miles southeast of Little Rock, the Associated Press reported. A post-crash fire engulfed the helicopter in flames, preventing first responders from approaching the crash site when they arrived. The Bell 407 helicopter, known as Pafford AIR ONE, was owned and operated by Pafford EMS and Air Methods. Pafford EMS confirmed no patients were on board at the time of the crash, but that the aircraft was flying from Pine Bluff to pick up a patient in West Helena. The three crew members who ... Read More

FDA raises concerns about herbal supplement kratom

The Food and Drug Administration (FDA) issued a Public Health Advisory due to its growing concerns about the risks associated with the use of the herbal supplement kratom, and is calling on those who believe in the potential medical benefits of the herb to conduct research on kratom so that its risks and benefits can be better understood. Kratom is a plant indigenous to Thailand, Malaysia, Indonesia and Papua New Guinea. It has grown in popularity in the U.S., and is often marketed as a “safe” treatment for a variety of conditions. The FDA said it knows people are using kratom ... Read More

Produce packer’s recall spurs chain reaction of recalls

Dozens of vegetable products are being pulled from grocery store shelves across the country after California-based Mann Packing announced it was recalling several of its products due to concerns that the vegetables had been contaminated with listeria, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and people with compromised immune systems. It can also cause miscarriages and stillbirths in pregnant women. Mann Packaging’s recall spurred a chain of recalls from other companies who carry or use Mann Packaging’s produce products. Meijer, a Midwestern chain similar to Walmart, recalled nearly 20 different ... Read More

Fresno Crash Survivor Says City Neglected Dangerous Intersection

If a city has received complaints about a dangerous intersection for more than three decades but failed to remedy the problem, is it liable when a motorist becomes seriously injured in a collision allegedly caused by the intersection’s poor design? That is the question a Fresno County Superior Court jury will have to consider in a case brought against the city by Steven Kennedy, 51, who was struck by a car while driving through the intersection of Cedar Avenue and Bulldog Lane – an extremely busy intersection near Fresno State University with no dedicated left-turn lights. Mr. Kennedy, a former ... Read More

Raw milk linked to Brucella bacteria exposure

Got raw milk? It’s a slogan used by Texas-based K-Bar dairy, which is currently in the limelight for illnesses spanning seven states linked to Brucella bacteria found in its raw milk, which had not undergone pasteurization to kill germs. The Centers for Disease Control and Prevention (CDC) and the Texas State Department of Health Services have received reports of people who drank K-Bar’s milk and have symptoms of brucellosis in Alabama, Arkansas, California, Ohio, North Dakota, Tennessee and Texas, according to a CDC press release. “It’s very important for people who drank raw milk from this dairy to seek treatment ... Read More

Physiomesh Found to be Shredded Inside Woman’s Abdomen

A new lawsuit against Ethicon and Johnson & Johnson was filed after a woman’s Physiomesh shredded inside her body. Jo Ann Lax of Lafe, Arkansas underwent a laparoscopic surgery to repair an umbilical hernia on Oct. 27, 2014. The surgeon, Dr. Robert Warner Jr., implanted Lax with Physiomesh 15×15 cm. in size. The mesh was designed to reinforce the tissue affected by the hernia, to allow Lax to return to life as normal. When Lax began experiencing pain at the hernia site, it was determined that the hernia mesh must have failed. On May 28, 2015, Lax underwent an additional surgery to have ... Read More

OriGen recalls defective catheters

OriGen Biomedical is recalling two lots of its VV28F Reinforced Dual Lumen ECMO Catheters because the clear extension tube may separate from the hub that it is inserted in, which could cause damage or impairment to the patient if there is not immediate intervention. To date, one adverse event related to these recalled products has been reported. The VV28F Reinforced Dual Lumen ECMO Catheters that fall under the recall include lot number N18487, with the manufacture date of Aug. 14, 2014, and the expiration date of Aug. 30, 2018; and the not number 18487-1, with the manufacture date of April ... Read More