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Recalls 1610 articles

Farm eggs linked to 38 cases of Salmonella infection

Gravel Ridge Farms, located in Cullman, Alabama, has issued a recall of Large Cage Free Eggs after samples collected during an inspection at the plant identified its shell eggs as linked to 38 cases of Salmonella Enteritidis illnesses. The recall involves both single dozen and 2.5 dozen flats of Gravel Ridge Farms Large Cage Free Eggs with the UPC 7-06970-18444-6 and the Use By Dates ranging from 7/25/18 through 10/3/18. The eggs were distributed between June 25 and Sept. 6, 2018, and were sold primarily in restaurants and retail stores in Alabama, Georgia and Tennessee. Customers who have purchased these ... Read More

Kellogg’s Honey Smacks linked to 135 Salmonella infections

At least 135 people in 36 states have fallen ill with Salmonella Mbandaka infections after eating Kellogg’s Honey Smacks Cereal, and at least 34 of them have been hospitalized, according to an Outbreak Update by the Food and Drug Administration (FDA). The FDA has been working with the Centers for Disease Control and Prevention (CDC) and state partners to collect information about the outbreak since a cluster of illnesses were identified on May 17 and traced it to the cereal. On June 14, Kellogg Company issued a recall on boxes of Honey Smacks throughout the United States including Guam and ... Read More

Nissan Recalls 215,000 Vehicles Over Brake Seal Fire Risk

Nissan has announced a recall of more than 215,000 model-year 2015-2018 cars and SUVs to fix a defect that could cause anti-lock brake fluid to leak onto an internal circuit board and start a fire or malfunction. The recall covers the 2015-2017 Nissan Murano, 2016 and 2017 Nissan Maxima, the 2017 and 2018 Nissan Pathfinder, and the 2017 Infiniti QX60. According to National Highway Traffic Safety Administration (NHTSA) recall documents, the problem stems from the antilock braking system’s actuator pump seal. The seal may allow brake fluid to leak out onto the electronic circuit board causing a short in the ... Read More

Ground beef products recalled due to E.coli scare

More than 132,600 pounds of ground beef products made from the chuck portion of the carcass are being recalled because the meat may be contaminated with Escherichia coli O26 (E. coli), a bacteria that can cause potentially life threatening illness in some humans. At least 17 people have been sickened and one person has died between July 5 and July 25, 2018, after eating the meat. The recall was initiated by Cargill Meat Solutions, a Fort Morgan, Colorado-based establishment. Affected ground beef products were produced and packaged on June 21, 2018, and bear the establishment number “EST. 86R” inside the ... Read More

Nissan Recalls Vehicles For Ignition Switch Defect

Nissan is recalling more than 165,000 vehicles in the U.S. and Canada to repair an ignition switch problem that could turn off the engine while the vehicle is in motion, resulting in the risk of a crash and deactivating the airbags. Although the National Highway Traffic Safety Administration (NHTSA) has yet to announce a recall of the Nissan vehicles, the Japanese automaker confirmed the recall to Consumer Reports. Canada’s transportation regulatory agency, Transport Canada, announced the Nissan recall on Aug. 22, saying that the problem stems from a spring in the ignition assembly that could wear out over time and ... Read More

More blood pressure pills recalled due to cancer-causing contaminant

The list of valsartan-containing blood pressure and heart failure drugs recalled due to the presence of a cancer-causing substance has once again expanded to include all lots of Torrent Pharmaceuticals Limited valsartan/amlodipine/HCTZ, valsartan/amlodipine, and valsartan tablets, according to the Food and Drug Administration (FDA). The recall was initiated on July 13 for certain valsartan tablets because they were found to contain a chemical known as N-nitrocodimethylamine (NDMA) in levels that exceeded those considered acceptable for public safety. The chemical is sometimes found in water supplies and food and is classified by the Environmental Protection Agency (EPA) as a probable human ... Read More

FDA expands recall of blood pressure drugs due to cancer-causing impurity

The list of blood pressure drugs recalled because they may contain a cancer-causing impurity has been expanded to include nearly five dozen products from 12 different pharmaceutical companies. On July 13, the Food and Drug Administration (FDA) first announced a recall of certain valsartan tablets because they were found to contain a chemical known a N-nitrocodimethylamine (NDMA) in levels that exceeded those considered acceptable for public safety. The chemical, which is sometimes found in water supplies and food, is classified by the Environmental Protection Agency (EPA) as a probable human carcinogen – something that can increase the risk of cancer ... Read More

Risk of Fire, Burn Injuries Prompts Three Product Recalls

The risk of overheating, fire, and burn injuries has triggered a nationwide recall of three consumer products in recent days, federal safety regulators announced. Zebra Technologies Printer Power Supply Units According to the U.S. Consumer Product Safety Commission (CPSC), Zebra Technologies is expanding a previous recall of the power supply units used on its thermal printers. The power supply units can degrade and corrode over time when exposed to moisture and overheat, posing a fire hazard. The CPSC said Zebra Technologies recalled about 166,000 of the power supply units in Dec. 2016 and then expanded the recall on Aug. 2, ... Read More

Cancer-causing impurity may have been present in blood pressure drugs for years

The presence of a potentially cancer-causing impurity in some brands of the blood pressure and heart failure drug valsartan may have been present in the products for as long as four years, the Food and Drug Administration (FDA) announced in a Safety Alert and update about the agency’s ongoing investigation into drugs possibly tainted with N-nitrosodimethylamine, or NDMA. Last week, the FDA announced three recalls related to the NDMA impurity detected in the valsartan active pharmaceutical ingredient (API): Teva Pharmaceuticals USA labeled as Major Pharmaceuticals – recall at the retail level because these products are only used in facilities where ... Read More

Del Monte Vegetable Trays Linked to Second Midwest Cyclospora Outbreak

Del Monte vegetable trays have been linked to one of two separate outbreaks of cyclospora parasite in the Midwestern U.S., public health officials warn. Combined, the cyclospora outbreaks have sickened at least 400 people in every Midwest state along with Montana, Kentucky, and West Virginia. The U.S. Centers for Disease Control and Prevention (CDC) reported 237 cases of cyclosporiasis in people who ate vegetables from Del Monte Fresh vegetable trays containing broccoli, cauliflower, carrots, celery, and dill dip. Reports of illnesses linked to cyclospora-contaminated Del Monte vegetable trays came from Iowa, Michigan, Minnesota, and Wisconsin. Of the people sickened after ... Read More