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Food and Drug Administration

McDonald's IDs Source Of E. Coli Outbreak Tied To Quarter Pounders McDonald's IDs Source Of E. Coli Outbreak Tied To Quarter Pounders
McDonald's IDs Source Of E. Coli Outbreak Tied To Quarter Pounders Health officials have pinpointed the specific ingredient that triggered an E. coli outbreak at McDonald’s that killed one person and sickened dozens more across several states. Testing done by the Colorado Department of Agriculture eliminated Quarter Pounder beef patties as the source of the outbreak, McDonald’s confirmed on Sunday, Oct. 27. That leaves the restaurant’s slivered onions, which are primarily used on Quarter Pounder hamburgers, as the likely source of contamination, according to the Food and Drug Administration (FDA). Earlier Report: E. Coli Outbreak Tied To McDonald'…
Popular Milk Product Recalled In 27 States, Including CT, Due To Allergy Risk Popular Milk Product Recalled In 27 States, Including CT, Due To Allergy Risk
Popular Milk Product Recalled In 27 States, Including CT, Due To Allergy Risk A nationwide recall has been issues for a popular brand of milk due to an allergy risk. HP Hood LLC is recalling 96-ounce containers of Lactaid Milk because the product may contain trace amounts of almond, which is not listed on the label.  People who have an allergy or severe sensitivity to almonds may run the risk of serious or life-threatening allergic reaction if they consume these products, according to an announcement by the Food and Drug Administration (FDA). The product was shopped to retailers and wholesalers in Alabama, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois…
Dollar Tree Sold Lead-Infused Applesauce Pouches For Weeks After Recall, FDA Says Dollar Tree Sold Lead-Infused Applesauce Pouches For Weeks After Recall, FDA Says
Dollar Tree Sold Lead-Infused Applesauce Pouches For Weeks After Recall, FDA Says Despite a recall notice and multiple warnings from the Food and Drug Administration, Dollar Tree continued to sell applesauce pouches containing lead for weeks, federal officials say. The popular retail chain was issued a letter from the FDA this month regarding the WanaBana fruit puree pouches, distributed by Negasmart. "As described below, laboratory analysis of multiple lots of WanaBana Apple Cinnamon Fruit Puree pouches, including finished product samples collected from Dollar Tree stores, detected extremely high concentrations of lead," the letter reads.  "... you conti…
Cucumbers Shipped To 14 States Recalled Due To Possible Salmonella Contamination Cucumbers Shipped To 14 States Recalled Due To Possible Salmonella Contamination
Cucumbers Shipped To 14 States Recalled Due To Possible Salmonella Contamination A Florida-based company is recalling whole cucumbers that were shipped to 14 states, but may be contaminated with Salmonella, the Food and Drug Administration (FDA) announced. According to the FDA, the cucumbers subject to recall are dark green, between 1.5 inches and two inches thick and between five to nine inches long. Officials made note that mini cucumbers and English cucumbers are not included in the recall. FDA The recalled cucumbers were shipped in bulk cartons between Friday, May 17 and Tuesday, May 21 to retail distribution centers, wholesalers, and food service distributor…
Planters Nuts Recalled Due To Listeria Contamination Concerns Planters Nuts Recalled Due To Listeria Contamination Concerns
Planters Nuts Recalled Due To Listeria Contamination Concerns A pair of Planters nuts products are being recalled due to possible contamination with the bacteria that causes listeria. Hormel Foods Sales, LLC is voluntarily recalling the two Planters products that were produced at one of its facilities in April, according to an announcement by the Food and Drug Administration (FDA). Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, sti…
Trader Joe's Recalling Basil Due To Salmonella Outbreak Trader Joe's Recalling Basil Due To Salmonella Outbreak
Trader Joe's Recalling Basil Due To Salmonella Outbreak Trader Joe's is recalling Infinite Herbs-brand organic basil that was sold across the country in 2.5-ounce clamshell packaging due to concerns of Salmonella contamination. This week, the supermarket giant issued an alert cautioning shoppers in 29 states, as well as Washington, DC, not to consume the product as the Food and Drug Administration (FDA) investigates a reported outbreak of Salmonella. Trader Joes is recalling Infinite Herbs Organic Basil FDA According to the FDA, "Trader Joe’s has already voluntarily removed all Infinite Herbs-brand organic basil packed in 2.5-oz clamshell pa…
Nationwide Recall Issued After E. Coli Outbreak Linked To Raw Milk Cheese Nationwide Recall Issued After E. Coli Outbreak Linked To Raw Milk Cheese
Nationwide Recall Issued After E. Coli Outbreak Linked To Raw Milk Cheese A new multistate E. coli outbreak linked to raw milk cheese has sickened nearly a dozen people and led to a recall, according to federal authorities. In a Food Safety Alert issued on Friday, Feb. 16, the US Centers for Disease Control and Prevention (CDC) said six of 10 illnesses reported in four states came from those who said they ate RAW FARM brand raw cheddar cheese. Four of those infected have been hospitalized and one developed hemolytic uremic syndrome, a serious condition that can cause kidney failure. No deaths have been reported. The agency said Raw Farm LLC has re…
Dole Recalls Salads Sold In 25 States Due To Possible Listeria Contamination Dole Recalls Salads Sold In 25 States Due To Possible Listeria Contamination
Dole Recalls Salads Sold In 25 States Due To Possible Listeria Contamination A recall has been issued for several Dole Fresh Vegetables salad kits due to possible Listeria contamination. Dole says the kits were processed on the same line as cheeses produced by Rizo-López Foods, which recalled a line of its dairy products, including cheeses. Related story - Deadly Cheeses Prompt Massive Recall Nationwide: CDC, FDA, USDA "This recall notification is being issued due to the potential for cross-contamination of cheese contained in certain master packs by cheese potentially contaminated with Listeria monocytogenes from our packaged cheese supplier," Dole sai…
Deadly Cheeses Prompt Massive Recall Nationwide: CDC, FDA, USDA Deadly Cheeses Prompt Massive Recall Nationwide: CDC, FDA, USDA
Deadly Cheeses Prompt Massive Recall Nationwide: CDC, FDA, USDA Dairy products linked to deaths and serious illness — sold nationwide at many major retailers — are being recalled, the Center for Disease Control, the US Department of Agriculture, and the Food And Drug Administration announced in multiple releases over the first week of February.  Rizo Lopez Foods, Inc. is recalling over 50 products after 26 illnesses, 23 hospitalizations, and 2 deaths, according to the CDC.  The California-based company issued the recall following the report of Listeria monocytogenes contamination causing illnesses in 11 states. Listeria monocytogene…
New Info On Pair Of Brands Released After Massive Nationwide Eye Drop Recall New Info On Pair Of Brands Released After Massive Nationwide Eye Drop Recall
New Info On Pair Of Brands Released After Massive Nationwide Eye Drop Recall A nationwide recall of more than two dozen eye drop products has just been amended. The original recall was announced this past November for 27 drops distributed to wholesalers and retailers by Velocity Pharma LLC. The recall was issued due to potential safety concerns after Food and Drug Administration (FDA) investigators found insanitary conditions. In a new announcement, the company said product details on two of the brands sold at outlets including Rite Aid have been corrected. The two drops and the changes are: Lubricant Gel Drops, 15 ml., Carboxymethylcellulose Sodium Ey…
NY Resident Dies In CT After Eating Mislabeled Cookies, Recall Issued NY Resident Dies In CT After Eating Mislabeled Cookies, Recall Issued
NY Resident Dies In CT After Eating Mislabeled Cookies, Recall Issued A young New Yorker is dead after eating a cookie at a Connecticut gathering that included peanuts - but didn’t say so on the label, officials said. Related story: Dancer Who Died After Eating Cookie With Nuts ID'd A limited-time batch of Florentine cookies, produced in Islip, New York, and sold at two Stew Leonard’s outlets in Connecticut -- in Danbury and Newington -- has been recalled after a person in their 20s reportedly died of an allergic reaction. The Connecticut State Department of Consumer Protection Food, Standards and Product Safety Division (DCP) announced the recall and a…
Popular Brand Of Turkey Gravy Recalled Due To Labeling Issue Popular Brand Of Turkey Gravy Recalled Due To Labeling Issue
Popular Brand Of Turkey Gravy Recalled Due To Labeling Issue A popular brand of turkey gravy is being recalled because of a mislabeling issue. Seneca Foods Corporation has announced a voluntary recall of mislabeled Hy-Vee Turkey gravy in glass jars that actually contain beef gravy.  The recall extends to the following labels and package sizes only: Hy-Vee Turkey Gravy (12 oz glass jars) UPC: 75450-03608 Individual Lot Code On Lid: A3CG162M A3CG192M "This product could potentially contain a soy allergen which is not declared on the label," the company said, noting that it is "now retrieving improperly labeled Hy-Vee Turkey Gravy from its distri…
Recall Issued By Ice Cream Manufacturer Due To Listeria Fears Recall Issued By Ice Cream Manufacturer Due To Listeria Fears
Recall Issued By Ice Cream Manufacturer Due To Listeria Fears A recall has been issued for a brand of ice cream, ice cream bars, yogurt, and gelato due to Listeria concerns. Vermont-based Wilcox Ice Cream says that one lot of the Super Premium Mint Chip manufactured on Tuesday, Nov. 14 may be contaminated with Listeria monocytogenes. In addition to the mint chip flavor, the company is recalling all other products manufactured at its facility during the same time period.  Products were distributed in retail stores and co-ops located in New York, Massachusetts, New Hampshire, and Vermont. The products, with best-by dates from 9/14/24 to 11/…
Nationwide Recall Issued For Peaches, Plums, Nectarines Sold At Stores Due To Listeria Risk Nationwide Recall Issued For Peaches, Plums, Nectarines Sold At Stores Due To Listeria Risk
Nationwide Recall Issued For Peaches, Plums, Nectarines Sold At Stores Due To Listeria Risk A nationwide recall has been issued for a brand of peaches, plums, and nectarines because of a possible health risk. The HMC Group Marketing, Inc., which does business as HMC Farms, issued the recall for the products sold in retail stores between Wednesday, May 1, and Wednesday, November 15, 2023, and the same date range in 2022, according to the Food and Drug Administration (FDA) website. The view product label photos, visit the FDA link here. The fruit is being recalled because it can potentially be contaminated with Listeria monocytogenes, an organism that can cause serious and sometime…
Massive New Nationwide Recall Issued For 27 Eye Drop Products Due To 'Insanitary Conditions' Massive New Nationwide Recall Issued For 27 Eye Drop Products Due To 'Insanitary Conditions'
Massive New Nationwide Recall Issued For 27 Eye Drop Products Due To 'Insanitary Conditions' A new nationwide recall has been issued for 27 eye drop products. The drops, distributed to wholesalers and retailers by Velocity Pharma LLC,  are being recalled due to potential safety concerns after Food and Drug Administration (FDA) investigators found insanitary conditions. All lots subject to the recall have expiration dates ranging from November 2023 to September 2025. For a table listing all 27 brands involved, click this link from the FDA. A risk statement accompanying the recall says: "For those patients who use these products, there is a potential risk of eye infections or…
New Ice Cream Recall Issued Due To Listeria Fears New Ice Cream Recall Issued Due To Listeria Fears
New Ice Cream Recall Issued Due To Listeria Fears A new ice cream recall has been issued because of Listeria concerns. The Life Raft Treats products were shipped by GoldBelly.com to 40 states, including New York, New Jersey, Connecticut, Massachusetts, Pennsylvania, Maryland, and Virginia. The recall covered these products: "Not Fried Chicken" - 64-ounce bucket (No UPC) and 2.5 oz. bar (UPC 8 60006 18210 6) "Life is Peachy"- 6-count box (No UPC) To view product packaging photos from the Food and Drug Administration (FDA), click here and scroll down. The company was notified last week by the South Carolina Department of Health and …
Cakes Sold Nationally At Walmart Recalled Due To Possible Peanut Presence: FDA Cakes Sold Nationally At Walmart Recalled Due To Possible Peanut Presence: FDA
Cakes Sold Nationally At Walmart Recalled Due To Possible Peanut Presence: FDA Check the fridge. The Food and Drug Administration (FDA) announced that it is recalling a specific cake that was sold at Walmart stores across the country due to a mislabeling issue. David's Cookies issued an alert regarding its "Marketside Chocolate Chip Explosion Cake" with the lot code (see above photo) of #BS23212 which may in fact be "Marketside Ultimate Peanut Butter Chocolate Cake."  According to the FDA, the recalled cakes were mislabeled and does not depict peanuts as a key ingredient in the item, and also lacks a peanut allergen warning. The recalled items are in a 7-ounce,…
New Ice Cream Recall Issued Due To Undeclared Ingredient New Ice Cream Recall Issued Due To Undeclared Ingredient
New Ice Cream Recall Issued Due To Undeclared Ingredient A new ice cream recall has been issued by a manufacturer in the region, this time due to an undeclared ingredient. Weis Markets Inc. said it is recalling containers of Weis Quality Brownie Moose Tracks Ice Cream (48 ounces) because the product may contain undeclared egg.  People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reactions if they consume this product, according to an announcement by the Food and Drug Administration (FDA). The product was distributed to all 197 Weis Markets’ retail stores throughout the Northeast and …
Frozen Vegetables Sold Nationwide Recalled Due To Concerns Of Listeria Contamination Frozen Vegetables Sold Nationwide Recalled Due To Concerns Of Listeria Contamination
Frozen Vegetables Sold Nationwide Recalled Due To Concerns Of Listeria Contamination A nationwide recall has been announced that involves several big brands, the Food and Drug Administration (FDA) announced. Washington-based Twin City Foods is voluntarily recalling not-ready-to-eat quick frozen "Super Sweet Corn" and "Mixed Vegetable" products that were sold nationwide and may be contaminated with Listeria monocytogenes.  The recalled items were sold at Kroger, Food Lion, and other grocery stores across the country. A complete list of recalled products and the specific lot codes associated with them can be found on the FDA website. The products subject to the recall.F…
These Eye Drop Products Could Cause Serious Health Risks, FDA Warns These Eye Drop Products Could Cause Serious Health Risks, FDA Warns
These Eye Drop Products Could Cause Serious Health Risks, FDA Warns Consumers are being warned by the Food and Drug Administration (FDA) to immediately stop using two eye drop products because of potential bacterial or fungal contamination that could cause serious health risks.  The advisory covers these products distributed by LightEyez Limited:  Dr. Berne's MSM Drops 5% Solution,  LightEyez MSM Eye Drops – Eye Repair. "Using contaminated eye drops could result in minor to serious vision-threatening infection which could possibly progress to a life-threatening infection," the FDA said. The Dr. Berne’s and LightEyez eye drop products also c…
Nationwide Nestlé Recall: Popular Cookie Dough May Have Wood Fragments Nationwide Nestlé Recall: Popular Cookie Dough May Have Wood Fragments
Nationwide Nestlé Recall: Popular Cookie Dough May Have Wood Fragments Nestlé USA has issued a voluntary recall of a limited quantity of one of its cookie dough products due to the potential presence of wood fragments. This voluntary recall is isolated to two batches of Nestlé Toll House Chocolate Chip Cookie Dough “break and bake” Bar products that were produced on Wednesday, April 24, and Thursday, April 25, 2023, and distributed at retailers throughout the nation, according to the Food and Drug Administration (FDA). The recall does not involve any other Nestlé  Toll House products, including other varieties of refrigerated cookie d…
Hospitalizations Lead To Ice Cream Recall In 19 States, Including NY: FDA Hospitalizations Lead To Ice Cream Recall In 19 States, Including NY: FDA
Hospitalizations Lead To Ice Cream Recall In 19 States, Including NY: FDA Hospitalizations have led a New York-based company to recall its packages of soft-serve ice cream — in 19 states, according to the Food and Drug Administration.  Two people have reported becoming ill in New York and Pennsylvania after consuming Soft Serve On The Go by Real Kosher Ice Cream of Brooklyn, according to the FDA recall notice issued on Wednesday, Aug. 9.  "Both individuals were hospitalized, but no deaths have been reported to date," the FDA said. After the first patient in Pennsylvania became ill, the state's Department of Agriculture tested samples of the product and found Li…
Frito-Lay Issues Recall For Tostitos Product That May Contain Undeclared Ingredient Frito-Lay Issues Recall For Tostitos Product That May Contain Undeclared Ingredient
Frito-Lay Issues Recall For Tostitos Product That May Contain Undeclared Ingredient A recall has been issued for a Tosititos product that may contain an undeclared ingredient. Frito-Lay today issued the voluntary recall for select 15 oz. Tostitos Avocado Salsa Jar Dips due to the possible presence of an undeclared milk allergen, according to an announcement by the Food and Drug Administration (FDA). "Those with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products," the announcement said. While the front of the affected jar is correctly labeled as Tostitos Avocado Salsa, the back of the jar …
Recall Issued For Frozen Fruit Product Due To Potential Hepatitis A Contamination Recall Issued For Frozen Fruit Product Due To Potential Hepatitis A Contamination
Recall Issued For Frozen Fruit Product Due To Potential Hepatitis A Contamination A manufacturer is recalling a frozen food product due to the potential to be contaminated with Hepatitis A. in cooperation with the Food and Drug Administration (FDA), Wawona Frozen Foods issued the recall for its Organic Daybreak Blend, 4-pound size because the frozen organic strawberries in the blend may have the potential to be contaminated with Hepatitis A. "Although Hepatitis A has not been detected in this product and there are no illnesses associated with the product, out of an abundance of caution, consumers should stop consuming the food," the FDA said. The recalled…
50,000-Plus Bottles Of Popular Brand Of Buffalo Wing Sauce Recalled 50,000-Plus Bottles Of Popular Brand Of Buffalo Wing Sauce Recalled
50,000-Plus Bottles Of Popular Brand Of Buffalo Wing Sauce Recalled A recall has been issued for a popular brand of buffalo wing sauce due to an undeclared ingredient. T.W. Garner Food Company is voluntarily recalling 50,688 12-ounce bottles of Texas Pete Buffalo Wing Sauce because some of the bottles may contain Texas Pete® Extra Mild Wing Sauce which contains soy, according to the Food and Drug Administration (FDA). People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reactions if they consume this product, the FDA noted The product can be identified as a 12 oz. glass bottle with…
Recall Issued For Lay’s Potato Chips Sold In 4 States, Including Connecticut Recall Issued For Lay’s Potato Chips Sold In 4 States, Including Connecticut
Recall Issued For Lay’s Potato Chips Sold In 4 States, Including Connecticut Check your chips. Frito-Lay has issued a voluntary recall for some of its Lay’s Classic Potato Chips that may contain undeclared milk ingredients from sour cream and onion potato chips, according to the Food and Drug Administration (FDA). The products were distributed to grocery, club and convenience stores in Connecticut, Massachusetts, Maine, and New Hampshire, and consumers would have been able to purchase them as early as April 16, 2023. The recall includes 13-ounce Lay’s Classic Party Size Potato Chips and 15 5/8-ounce Lay’s Classic Mix and Match Potato Chips. The 13-o…
COVID-19: Do Not Use These At-Home Tests Due To Bacteria Concerns, FDA Says COVID-19: Do Not Use These At-Home Tests Due To Bacteria Concerns, FDA Says
Covid-19: Do Not Use These At-Home Tests Due To Bacteria Concerns, FDA Says Americans have been advised by federal officials not to use a brand of COVID-19 at-home tests that could have potentially harmful bacteria inside the kits. SD Biosensor, Inc. announced on Friday, May 5, that the company is requesting that consumers stop using “Pilot COVID-19 At-Home Tests” due to contaminants found in the tube with liquid inside, according to the Food and Drug Administration (FDA). Related story - COVID-19: These Pair Of Symptoms Distinguish Arcturus From Other Omicron Subvariants The affected tests can be identified by the lot number on the outer packaging (see below…
Gold Medal Flour Products Recalled Due To Salmonella Contamination Gold Medal Flour Products Recalled Due To Salmonella Contamination
Gold Medal Flour Products Recalled Due To Salmonella Contamination General Mills is recalling Gold Medal flour products after Salmonella has turned up in testing. The company announced on Friday, April 28 a voluntary national recall of 2-, 5- and 10-pound bags of its Gold Medal Unbleached and Bleached All Purpose Flour with a “better if used by” date of March 27, 2024, and March 28, 2024.  The recall is being issued for the potential presence of Salmonella Infantis, which was discovered during sampling of the 5-pound bag product, the Food and Drug Administration (FDA) said. All other types of Gold Medal Flour are not affected by this recall…
Eye Drops Tainted With Bacteria Linked To Deaths, Infections, CDC Says Eye Drops Tainted With Bacteria Linked To Deaths, Infections, CDC Says
Eye Drops Tainted With Bacteria Linked To Deaths, Infections, CDC Says The Centers for Disease Control and Prevention (CDC) is warning about eye drops tainted with bacteria that are now being linked to three deaths and dozens of infections. In addition, eight people have reported vision loss and there have been four reports of eyes being removed after the drops were used. A total of 68 people in 16 states have been identified as having infections of a rare strain of drug-resistant Pseudomonas aeruginosa never before reported in the United States before this outbreak, according to the CDC. The outbreak is associated with multiple types of infections, including…
COVID-19: Subvariant XBB Accounts For 70% Of Tristate NY Cases, Sparking Concerns Of New Wave COVID-19: Subvariant XBB Accounts For 70% Of Tristate NY Cases, Sparking Concerns Of New Wave
Covid-19: Subvariant XBB Accounts For 70% Of Tristate NY Cases, Sparking Concerns Of New Wave An Omicron strain called XBB.1.5 which now accounts for the majority of COVID-19 cases from the New York tristate area through New England has the potential to trigger a new wave of infections, a top expert is now saying. The XBB.1.5 variant makes up 40.5 percent of cases in the United States, and 70 percent of cases in the New York tristate area through New England, according to the Centers for Disease Control and Prevention (CDC). "I would expect a wave of infection with this new variant," Dr. Scott Gottlieb, former commissioner of the Food and Drug Administration (FDA), told MS…
COVID-19: Vaccine Targeting Omicron Variant Authorized For Young Children By FDA COVID-19: Vaccine Targeting Omicron Variant Authorized For Young Children By FDA
Covid-19: Vaccine Targeting Omicron Variant Authorized For Young Children By FDA The Food and Drug Administration has authorized the use of updated COVID-19 booster shots targeting the Omicron variant for younger children. The FDA announced the amended emergency use authorization of the bivalent Moderna and Pfizer booster vaccines on Wednesday, Oct. 12. Today, FDA amended the EUA of the Moderna COVID-19 Vaccine, Bivalent and the Pfizer-BioNTech COVID-19 Vaccine, Bivalent to authorize their use as a single booster dose in younger age groups. https://t.co/C2Sx5Nkk0R pic.twitter.com/xsPfO2Mek3 — U.S. FDA (@US_FDA) October 12, 2022 The Moderna bivalent booster is autho…