Apr 25, 2018
Posted April 20, 2018 4:00 PM EST. What's New? Based on new information, CDC is expanding its warning to consumers to cover all types of romaine lettuce from the Yuma, Arizona growing region. This warning now includes whole heads and hearts of romaine lettuce, in addition to chopped romaine and salads and salad ...
Case Count Maps · Advice to Consumers · Epi Curve · Signs and Symptoms
It hasn't been recalled, but the CDC recommends tossing out any heads or chopped romaine lettuce.
Apr 25, 2018
Author: 10News Staff
Published: 9:12 PM EDT April 24, 2018
Updated: 9:13 PM EDT April 24, 2018
Ice pops sold in several states are being recalled because of listeria fears.
The Ziegenfelder Company of Wheeling, West Virginia, is voluntarily recalling around 3,000 cases of Budget $aver Cherry Pineapple Monster Pops and Sugar-Free Twin Pops because they may be contaminated with Listeria monocytogenes, according to the FDA.
The ice pops were sold in Alabama, Arkansas, Florida, Maine, Missouri, Nebraska, Nevada, New Mexico, New York, Ohio, Oklahoma, Texas, Utah, Washington and Wyoming. They were delivered to those stores from April 5 through April 19.
So far, no illnesses have been reported.
The frozen products were sold 12 to a package under the brand names Budget $aver Cherry Pineapple Monster Pops and Sugar-Free Twin Pops. The Cherry Pineapple Monster Pops carry the UPC code 0-74534-84200-9, and have lot codes D09418A through D10018B. The Sugar-Free Pops carry the UPC code 0-74534-75642-9, and have lot codes D09318A through D10018B. Below are front and back representations of the packaged products as they appear in stores.
If you have them, take them back to the store where they were bought to get a full refund. If you have questions, call the company at 1-888-683-0379 Monday through Friday from 8am to 8pm.
May 27, 2017
May 25, 2017
John Morrell and Co. Recalls Beef Frank Products Due to Possible Foreign Matter Contamination
Class II Recall 052-2017
Health Risk: Low May 19, 2017
Congressional and Public Affairs
WASHINGTON, May 19, 2017– John Morrell and Co., a Cincinnati, Ohio establishment, is recalling approximately 210,606 pounds of ready-to-eat hot dog products that may be contaminated with extraneous materials, specifically metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The beef franks items were produced on January 26, 2017. The following products are subject to recall: [View Labels (PDF only)]
14 oz. sealed film packages containing “Nathan’s SKINLESS 8 BEEF FRANKS,” with a Use By date of Aug. 19, 2017.
16 oz. sealed film packages containing “Curtis BEEF MASTER Beef Franks,” with a Use By date of June 15, 2017.
The products subject to recall bear establishment number “EST. 296” on the side of the package. These items were shipped to retail locations nationwide.
The problem was discovered after the establishment received three complaints of metal objects in the beef frank product packages. The establishment notified FSIS on May 19, 2017.
There have been no confirmed reports of adverse reactions or injury due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers with questions about the recall can call 1 (877) 933-4625. Media with questions about the recall can contact Kathleen Kirkham, director of corporate communications, at (757) 365-1965.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: fsis.usda.gov/reportproblem.
Dec 22, 2016
This just in (well, as of yesterday): Cuisinart has recalled roughly 8 million (!) food processor blades, because "the food processor’s riveted blade can crack over time and small metal pieces of the blade can break off into the processed food." This recall applies to food processors purchased as far back as July 1996 (who can even remember what that year looked like?) and December 2015.
In other words, if you have a Cuisinart food processor, you probably have a blade that might be adding tiny pieces of metal to your food.
According to NPR, the recall was issued "after 69 consumers reported finding broken pieces of blade in their food."
And while finding sharp metal baked into a pie crust is good for prisoners, it can put a damper on your holiday party.
To see if your Cuisinart is affected, head to recall.cuisinart.com and follow the directions. The first thing you'll need to do is check to see if your blade has rivets on it. No rivets, no problem—your blade is not being recalled.
If you find that your blade is in fact being recalled? Stay calm, sister! Just call 1-877-339-2534 and Cuisinart will arrange to send you a new blade. In the meantime, put your Cuisinart aside. Perhaps break out your powerhouse blender instead?
Picture of my blade - Click to enlarge, then note the hairline cracks circled in red
Dec 14, 2016
Tuesday December 13 2016
Several brands of children’s medicine are on the recall list because they could be poisonous. The medicines are sold at CVS pharmacy stores and have the CVS name on the boxes.
The recalled medicines include the Kid’s Relief Homeopathic Ear Relief Liquid, Kids Relief Homeopathic Ear Relief Oral Liquid and infants’ teething tablets. The products were distributed to CVS stores nationwide. The company says there may be too much belladonna in the medications.
According to the U.S. Food and Drug Administration, belladonna can be dangerous or fatal when consumed in large doses.
According to Wikipedia, Atropa belladonna, commonly known as belladonna or deadly nightshade, is a perennial herbaceous plant in the Nightshade family (which includes tomatoes, potatoes, eggplant, etc.)
The root of the plant is generally the most toxic part, though this can vary from one specimen to another. Belladonna leaves and berries are gathered when the the berries are almost ripe and alkaloid content is greatest which makes them suited for medicinal use.
The leaves and berries are then dried in a dark and dry place and stored airtight. Fresh belladonna berries are mashed, fermented, and distilled into alcohol. Belladonna dosage depends on the user’s age and health condition. Consumption of one or two fresh belladonna berries mildly affects perception in adults. This effect outsets in one or two hours after the berries have been ingested. Three to four fresh berries act as a psychoactive aphrodisiac, and three to ten berries are a hallucinogenic dose. The lethal dose for adults is ten to twenty berries, depending on the physiological constitution of the consumer. Consumption of two or three berries by children can be lethal.
These data notwithstanding, consumption of belladonna should be mindful and generally avoided due to the devastating toxic states that can for some individuals prove lethal even with the minimal dosage.
Despite its dangerous characteristics, in controlled settings, belladonna does have many pharmacological uses.
If you have any of these products, stop using it immediately and call the Raritan Company at 1-866-467-2748 (Monday-Friday from 8am to 5:30pm EST).