Bacteria Strain Linked To Eyedrops That Killed, Led To Eyeball Removal: CDC Bacteria Strain Linked To Eyedrops That Killed, Led To Eyeball Removal: CDC
Bacteria Strain Linked To Eyedrops That Killed, Led To Eyeball Removal: CDC The Centers for Disease Control and Prevention (CDC) is teaming with the Food and Drug Administration (FDA) to investigate an infection linked to select eye drops that have led to multiple deaths and forced others to remove their eyes through surgery. Consumers are being advised to stop using EzriCare or Delsam Pharma’s Artificial Tears products as they continue to investigate a multi-state outbreak of “an extensively drug-resistant strain of Pseudomonas aeruginosa.” According to the CDC, infections usually occur in people in the hospital or with weakened immune systems. It is partic…
Recall Issued For Popular Ice Cream Product Sold In NJ Due To Undeclared Allergens Recall Issued For Popular Ice Cream Product Sold In NJ Due To Undeclared Allergens
Recall Issued For Popular Ice Cream Product Sold In NJ Due To Undeclared Allergens A popular ice cream product sold throughout the region is being recalled due to reported undeclared allergens, the Food and Drug Administration (FDA) announced. Weis Markets has issued a voluntary recall of 48-ounce containers of its “Weis Quality Sea Salt Caramel Ripple Ice Cream,” which could potentially contain undeclared soy and coconut allergens. Officials say that anyone who has an allergy or severe sensitivity to soy or coconut allergens could run the risk of serious or life-threatening reactions if they are consumed. According to the FDA, the products may have been distributed in…
Nationwide Recall Issued For Cheese Products Due To Potential Listeria Contamination Nationwide Recall Issued For Cheese Products Due To Potential Listeria Contamination
Nationwide Recall Issued For Cheese Products Due To Potential Listeria Contamination A manufacturer has issued a nationwide recall for two of its brands of cheese because of potential contamination with Listeria, the Food and Drug Administration announced on Friday, Sept. 30. Old Europe Cheese, Inc. of Benton Harbor, Michigan is recalling its Brie and Camembert cheeses due to the concerns of 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.  Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stif…
CDC Warns Of Rise In Melatonin Poisoning In Kids Nationwide CDC Warns Of Rise In Melatonin Poisoning In Kids Nationwide
CDC Warns Of Rise In Melatonin Poisoning In Kids Nationwide Health officials are warning of an increase in melatonin poisoning among children. Over the past decade, the number of pediatric ingestions of melatonin rose 530%, with more than 260,000 ingestions reported between 2012 and 2021, according to the Centers for Disease Control and Prevention (CDC). Melatonin became the most frequently ingested substance among kids reported to national poison control centers in 2020, the CDC said. Melatonin is a hormone naturally produced by the body that regulates sleep-wake cycles, but is also sold as supplements. While the supplements are regulated by the …
Hepatitis A Outbreak Linked To Strawberries Sold At These Supermarkets Hepatitis A Outbreak Linked To Strawberries Sold At These Supermarkets
Hepatitis A Outbreak Linked To Strawberries Sold At These Supermarkets An outbreak of hepatitis A linked to strawberries is under investigation in the United States and Canada, the Food and Drug Administration said. The multi-state, multi-territory outbreak is potentially connected to fresh organic strawberries branded as FreshKampo and HEB, purchased between Saturday, March 5, 2022, and Monday, April 25, 2022. The products were sold at the following retailers, including, but not limited to: Aldi HEB Kroger Safeway Sprouts Farmers Market Trader Joe’s Walmart Weis Markets WinCo Foods A total of 17 illnesses and 12 hospitalizations have been reported nationwid…
JIF Peanut Butter Products Recalled After 14 People Sickened: CDC JIF Peanut Butter Products Recalled After 14 People Sickened: CDC
JIF Peanut Butter Products Recalled After 14 People Sickened: CDC A variety of JIF peanut butter products have been recalled amid a multi-state salmonella outbreak. The Jif products were sold at stores nationwide, according to the Food and Drug Administration. Many types and sizes were recalled, including creamy, crunchy, natural, and reduced fat. The lot code numbers are 1274425 through 2140425. A total of14 illnesses and two hospitalizations have been reported in the 12 states shown here. The back label of the recalled Jif brand peanut butter.CDC "Check your home for recalled Jif brand peanut butter," the Centers for Disease Control and Prevention…
Nationwide Recall Issued For Brand Of Supplements Due To 'Serious Health Risks,' FDA Says Nationwide Recall Issued For Brand Of Supplements Due To 'Serious Health Risks,' FDA Says
Nationwide Recall Issued For Brand Of Supplements Due To 'Serious Health Risks,' FDA Says Photo Credit: Kratom Strains A recall has been issued for a supplement after the products were found to be tainted with an undeclared drug that could cause serious health issues. Esupplementsales, LLC is recalling lot number 2107 of "Hard Dawn Rise and Shine" capsules, which were discovered to be tainted with tadalafil, an ingredient found in an FDA-approved product for the treatment of erectile dysfunction, according to an announcement posted to the Food and Drug Administration's website on Friday, Jan. 28. "The presence of tadalafil in Hard Dawn Rise and Shine Ca…
Federal Judge In NJ Orders Duo To Stop Selling Supposed COVID 'Cure' Federal Judge In NJ Orders Duo To Stop Selling Supposed COVID 'Cure'
Federal Judge In NJ Orders Duo To Stop Selling Supposed COVID 'Cure' UPDATE: A federal judge has issued a final order to a retired New Jersey lawyer and formerly licensed psychiatrist from Westchester to stop selling unapproved and misbranded drugs advertised as a cure for COVID-19. Ralph Fucetola of Newton and his partner, Rima Laibow, formerly of Croton-on-Hudson, sold a product that they claimed would "cure, mitigate, treat or prevent" the coronavirus, the Justice Department said Tuesday. They claimed that anyone who ingested one capful a day of "Dr. Rima Recommends Nano Silver 10PPM" should have "no fear or concern" about the coronavirus, a complaint on …
Cupcakes Recalled Due To Possible Metal Mesh Wire Contamination Cupcakes Recalled Due To Possible Metal Mesh Wire Contamination
Cupcakes Recalled Due To Possible Metal Mesh Wire Contamination A company is recalling packs of cupcakes because they might be contaminated with tiny fragments of metal mesh wire. Flowers Foods, Inc. announced on Sunday, Oct. 31, that it is recalling the Tastykake multi-pack cupcakes after receiving notification from a vendor that they could be contaminated.  The recalled products were distributed in New York, Delaware, Maryland, New Jersey, Pennsylvania, Virginia, Washington DC and West Virginia, the company said.  No injuries have been linked to the recalled products, Flowers Foods said.  The following products are included in the recall: Recal…
NJ Company's 223,000 Pounds Of Ready-To-Eat Salad Products Recalled NJ Company's 223,000 Pounds Of Ready-To-Eat Salad Products Recalled
NJ Company's 223,000 Pounds Of Ready-To-Eat Salad Products Recalled More than 200,000 pounds of pre-packaged salad products from a New Jersey company are being recalled due to misbranding and undeclared allergens. Ready Pac Foods East Coast establishments announced a recall of approximately 222,915 ready-to-eat salad products with meat and poultry because the products contain Food and Drug Administration (FDA) regulated salad dressing that has been recalled by the producer, Litehouse Inc., due to misbranding and an undeclared allergen that could impact some consumers. According to the US Department of Agriculture’s Food Safety and Inspection Service (FSIS),…
COVID-19: Moderna Seeks Full FDA Vaccine Approval COVID-19: Moderna Seeks Full FDA Vaccine Approval
Covid-19: Moderna Seeks Full FDA Vaccine Approval With six months having passed since Moderna began clinical trials for its COVID-19 vaccine, the pharmaceutical company is seeking full approval from the Food and Drug Administration. Moderna, which currently has emergency use authorization from the FDA to distribute its vaccine, reported in its latest trial data that it has proven 90 percent effective in preventing the symptoms of COVID-19, and 95 percent effective in the most severe cases of the virus. Currently, no COVID-19 vaccine is fully approved by the FDA, but three - Moderna, Pfizer, and the currently questionable Johnson & John…
COVID-19: Here's When Moderna Booster Shot Will Be Available For Those Who Got Both Doses COVID-19: Here's When Moderna Booster Shot Will Be Available For Those Who Got Both Doses
Covid-19: Here's When Moderna Booster Shot Will Be Available For Those Who Got Both Doses Moderna is working on a booster shot for its two-dose COVID-19 vaccine that will be made available by the fall to help avoid another surge of new cases over the winter. CEO Stephane Bancel said on CNBC that the company “wants to make sure there are boost vaccines available in the fall so that we protect people as we go into the next fall and winter season in the U.S.” Last month, the National Institutes of Health began testing several versions of boosters from Moderna that could potentially be used to combat variants of COVID-19, including the South African strain that has flummoxed resear…