Fair 21°
Tag:

FDA

News
Nationwide Recall Issued For Brand Of Eye Drops Over Contamination Risk Nationwide Recall Issued For Brand Of Eye Drops Over Contamination Risk
Nationwide Recall Issued For Brand Of Eye Drops Over Contamination Risk A nationwide recall has been issued for a specific lot of eye drops due to potential fungal contamination, which could cause serious eye infections. The recall involves lubricant eye drops under the Systane brand, manufactured by Alcon Laboratories, following a report of fungal material found in a sealed vial.  No illnesses have been reported, but fungal contamination can pose vision-threatening risks and, in rare cases, life-threatening complications for immunocompromised individuals. Details of the recall: Specific brand: Systane Lubricant Eye Drops Ultra PF, Single Vials On-…

SHARE

by Joe Lombardi
News
These Over-The-Counter Decongestants Don't Work, FDA Says These Over-The-Counter Decongestants Don't Work, FDA Says
These Over-The-Counter Decongestants Don't Work, FDA Says A common ingredient found in most oral over-the-counter cold medicines should be removed from the market because it doesn’t work, the Food and Drug Administration (FDA) says. This follows an extensive review that found the drug ineffective for treating nasal congestion. Oral phenylephrine, widely marketed in cold and allergy medications, has been in use for decades as a go-to nasal decongestant.  However, an FDA review, backed by last year’s unanimous recommendation from the Nonprescription Drug Advisory Committee, found that phenylephrine in oral form does not deliver effective conge…

SHARE

by Joe Lombardi
News
FDA Approves Updated COVID-19 Vaccines: Here's When They Will Be Available FDA Approves Updated COVID-19 Vaccines: Here's When They Will Be Available
FDA Approves Updated Covid-19 Vaccines: Here's When They Will Be Available The US Food and Drug Administration has just approved new COVID-19 vaccines.It marks the third time the vaccines from Pfizer and Moderna have been updated to match circulating strains since the original shot. The shots should be available within days, the FDA said in making the announcement Thursday afternoon, Aug. 22. The new vaccines have been updated with a formula to more closely target currently circulating variants and provide better protection against serious consequences of COVID, including hospitalization and death. “Vaccination continues to be the cornerstone of COVID-19 preventi…

SHARE

by Joe Lombardi
News
Popular Ice Cream Products Recalled Over Listeria Concerns, FDA Says Popular Ice Cream Products Recalled Over Listeria Concerns, FDA Says
Popular Ice Cream Products Recalled Over Listeria Concerns, FDA Says Approximately 70 ice cream products sold by multiple brands including Friendly's and Hershey's are being recalled due to a possible presence of listeria, the US Food and Drug Administration (FDA) said. The brands were recalled this week by Totally Cool, Inc. based in Owings Mills, MD, which has stopped the production and distribution of the affected products due to FDA sampling. Some of the most popular items recalled include: Friendly's 60 fl oz Celebration Ice Cream Cake 40 fl oz Strawberry Krunch Ice Cream Cake; Hershey's 38 fl oz vanilla and chocolat…

SHARE

by Cecilia Levine
Business
Nationwide Recall Issued For Ground Black Pepper Due To Possible Health Risk Nationwide Recall Issued For Ground Black Pepper Due To Possible Health Risk
Nationwide Recall Issued For Ground Black Pepper Due To Possible Health Risk A nationwide recall has been issued for a brand of ground black pepper that could be contaminated with Salmonella. UBC Food Distributors issued the recall for the product under the Baraka brand name in 7-ounce plastic containers with UPC code 8 22514 26626 6, the Food & Drug Administration (FDA) announced. The company said it was notified of the potential for contamination based on a routine state surveillance sample collected by the New York Department of Agriculture and Markets that tested positive for Salmonella the presence of Salmonella in some packages of the product. Salmon…

SHARE

by Joe Lombardi
Business
Popular Apple Juice Brand Recalled Due To High Arsenic Levels Popular Apple Juice Brand Recalled Due To High Arsenic Levels
Popular Apple Juice Brand Recalled Due To High Arsenic Levels A recall has been issued for a popular brand of apple juice due to high levels of arsenic. S. Martinelli & Co. said the recall is for a single lot of Martinelli’s Apple Juice, one-liter (33.8-ounce) bottles.  The recalled product has a “Best By” date of “09MAR2026” or “10MAR2026” on the front of the bottle above the label.  The product was shipped between March 13, 2023, and September 27, 2023, with the majority of the product shipped before July 28, 2023. This recall results from a sampling by the State of Maryland that found samples from one produc…

SHARE

by Joe Lombardi
News
FDA Recalls Westport Oysters After Norovirus Outbreak FDA Recalls Westport Oysters After Norovirus Outbreak
FDA Recalls Westport Oysters After Norovirus Outbreak The US Food and Drug Administration has recalled oysters grown and harvested in Connecticut following an outbreak of norovirus. In a notice on Thursday, March 14, the FDA said the outbreak was caused by oysters sold by Norwalk-based Norm Bloom and Son harvested in February. Although the FDA did not give many how many people were sickened, they did reveal the contaminated batch was associated with an outbreak in Minnesota. In the notice, the FDA warned consumers that the oysters were also sold to restaurants and retailers throughout Connecticut, Florida, Georgia, Maine, Maryl…

SHARE

by Kathy Reakes
Business
Recall Issued For Multiple Eye Ointment Brands Due To Possible Risk Of Infection Recall Issued For Multiple Eye Ointment Brands Due To Possible Risk Of Infection
Recall Issued For Multiple Eye Ointment Brands Due To Possible Risk Of Infection A recall has been issued for multiple brands of eye ointment products due to the "lack of sterility assurance at the facility" of the manufacturer during an inspection conducted by the Food and Drug Administration (FDA). "For those patients who use these products, there is a potential risk of eye infections or related harm," the FDA said. "These products are intended to be sterile. Ophthalmic drug products pose a potentially heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses."  Brassica Pharma Pvt. Ltd. is voluntarily recalling…

SHARE

by Joe Lombardi
Lifestyle
Contamination Concerns Prompt Nationwide Robitussin Cough Syrup Recall Contamination Concerns Prompt Nationwide Robitussin Cough Syrup Recall
Contamination Concerns Prompt Nationwide Robitussin Cough Syrup Recall Two types of Robitussin cough syrup products sold nationwide are being recalled due to potential microbial contamination, federal authorities announced. This week, New Jersey-based Haleon announced a recall of several lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult that could be contaminated, according to the US Food and Drug Administration (FDA). Recalled items include:  Four- and eight-ounce Robitussin Honey CF Max Day Adult with these lot numbers/expiration dates:  T18010 with an expiration date of Oct. 31, 2025; T08730 with an…

SHARE

by Zak Failla
Business
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…

SHARE

by Joe Lombardi
Business
Raw Dog, Cat Food Sold In CT Being Recalled Due To Contamination Concerns Raw Dog, Cat Food Sold In CT Being Recalled Due To Contamination Concerns
Raw Dog, Cat Food Sold In CT Being Recalled Due To Contamination Concerns The FDA is expanding a recall on a popular raw pet food product that could possibly be contaminated by Salmonella or Listeria monocytogenes, authorities announced. Earlier this month, Blue Ridge Beef began recalling certain lots of their "Kitten Grind," "Puppy Mix," and "Kitten Mix," after the company notified the North Carolina Department of Agriculture and Consumer Services that a sample had tested positive. The products subject to the recall were distributed between Nov. 14 and Dec. 20 packaged in clear plastic sold primarily at stores in these states:  Connecticut; Massachus…

SHARE

by Zak Failla
Business
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…

SHARE

by Joe Lombardi
Business
Stop Using These Eye Drop Products Sold At CVS, Rite Aid, Target Due To Infection Risk: FDA Stop Using These Eye Drop Products Sold At CVS, Rite Aid, Target Due To Infection Risk: FDA
Stop Using These Eye Drop Products Sold At CVS, Rite Aid, Target Due To Infection Risk: FDA Consumers should stop using more than two dozen over-the-counter eye drop products because of the risk of eye infections that may lead to vision loss or blindness. Click here for a new, updated story - Massive Eye Drop Recall Expands: 3 New Products Added As List Hits 29; Here's New Rundown The 26 products are from these brands: CVS Health, Leader (Cardinal Health), Rugby (Cardinal Health), Rite Aid, Target Up&Up, and Velocity Pharma. The alert comes after FDA investigators found bacterial contamination in critical drug production areas of a manufacturing facility. For the comp…

SHARE

by Joe Lombardi
Business
Van Leeuwen Recalls 4,000 Ice Cream Pints Due To Undeclared Ingredient Van Leeuwen Recalls 4,000 Ice Cream Pints Due To Undeclared Ingredient
Van Leeuwen Recalls 4,000 Ice Cream Pints Due To Undeclared Ingredient More than 4,000 pints of ice cream are being recalled by a New York-based manufacturer due to an undeclared ingredient. Van Leeuwen Ice Cream of Brooklyn says frozen 14-ounce pints of its French Ice Cream product "Brown Sugar Chunk” may contain an undeclared allergen, walnuts.  "People who have an allergy or severe sensitivity to walnuts run the risk of a serious or life-threatening allergic reaction if they consume these products," according to the FDA. The recalled products are distributed nationally in retail stores.  The product comes in a reddish-brown package with black le…

SHARE

by Joe Lombardi
Business
Company Issues Recall For Frozen Fruit Products Due To Hepatitis Outbreak Company Issues Recall For Frozen Fruit Products Due To Hepatitis Outbreak
Company Issues Recall For Frozen Fruit Products Due To Hepatitis Outbreak A company has issued a recall for various frozen food products sold at Costco, Aldi, Trader Joe's, and other businesses due to a hepatitis outbreak. Scenic Fruit Company said it is recalling frozen organic strawberries sold at Costco and Aldi, and frozen organic tropical blend sold to Trader Joe’s due to an outbreak of Hepatitis A illnesses. Although Hepatitis A has not been detected in this product, out of an abundance of caution, consumers should stop consuming the product and return it to their local store for a refund, the FDA said. The company has ceased the production and distributio…

SHARE

by Joe Lombardi
Business
Recall Issued For Popular Rao's Specialty Food Product Recall Issued For Popular Rao's Specialty Food Product
Recall Issued For Popular Rao's Specialty Food Product A recall has been issued for a popular Rao's Homemade Brand specialty food product. Sunny Dell Foods is recalling its 12-ounce jars of Rao’s Homemade Brand Roasted Red Peppers with Portobello Mushrooms because the affected jars of the condiment may contain undeclared tree nuts (pine nuts), the FDA announced.  People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reactions if they consume these products. The recalled products were distributed across retail stores in the Northeast US and through mail order e-commerce. The pro…

SHARE

by Joe Lombardi
Business
Recall Issued For Brand Of Mushrooms Due To Possible Health Risk Recall Issued For Brand Of Mushrooms Due To Possible Health Risk
Recall Issued For Brand Of Mushrooms Due To Possible Health Risk A Brooklyn-based company is recalling Enoki mushrooms that were imported from Korea which may be contaminated with Listeria monocytogenes. The FDA announced that H&C Food Inc. is recalling 7.05-ounce Enoki mushrooms that were important from Green Co. and distributed to supermarkets in New York, Maryland, and Virginia. The mushrooms subject to recall were distributed between Saturday, Feb. 15 and Thursday, March 5. According to the FDA, the mushrooms were sold in a clear plastic packaging with a green label, UPC code of 831211204181, and “H&C Food Inc.” on the back of the package. …

SHARE

by Zak Failla
Business
Nationwide Recall Issued For Hand Sanitizer Brand Due To Potential Contamination Nationwide Recall Issued For Hand Sanitizer Brand Due To Potential Contamination
Nationwide Recall Issued For Hand Sanitizer Brand Due To Potential Contamination A company has recalled bottles of hand sanitizer that may be contaminated with methanol. Adam's Polishes LLC recalled several lots of Adam’s Polishes Hand Sanitizer after FDA testing found that lot 133475 contains undeclared methanol, the company announced on Saturday, Nov. 5. Find the list of recalled lot numbers here. The hand sanitizer products were distributed nationwide to online customers between June 2020 and March 2022, Adam's Polishes said.  The company said those who accidentally ingest the products are at risk of methanol poisoning, which can cause comas, seizure…

SHARE

by Nicole Valinote
Business
Recall Issued For Supplement Due To Presence Of Undeclared Ingredient Recall Issued For Supplement Due To Presence Of Undeclared Ingredient
Recall Issued For Supplement Due To Presence Of Undeclared Ingredient A company recalled a supplement that was sold across the United States due to the presence of an undeclared ingredient.  Distributor RFR LLC recalled SANGTER Energy Supplements 3000mg with expiration date 01/2025 after Food & Drug Administration analysis found the products contained undeclared sildenafil, a substance found in FDA-approved treatments of male erectile dysfunction, according to an FDA announcement on Tuesday, Aug. 2. The presence of sildenafil makes the supplements an unapproved new drug, the FDA reported.  Undeclared sildenafil can interact with nitrates f…

SHARE

by Nicole Valinote
Business
Recall Issued For Supplement Sold On Amazon Due To Presence Of Unapproved Ingredient Recall Issued For Supplement Sold On Amazon Due To Presence Of Unapproved Ingredient
Recall Issued For Supplement Sold On Amazon Due To Presence Of Unapproved Ingredient Cartons of supplement products that were sold on Amazon are being recalled due to the presence of an undeclared, unapproved ingredient.  Ultra Supplement LLC announced the recall of cartons of its Sustango capsules packaged in 10-count blisters on Thursday, July 21. The company recalled products with lot number DAP272109 with an expiration date of 4/1/26 after laboratory analysis found that the products were contaminated with tadalafil, an ingredient in FDA-approved products for treatment of male erectile dysfunction. The presence of the ingredient makes the product an unapp…

SHARE

by Nicole Valinote
News
COVID-19: New Wave With 'Worst Version' Of Omicron Starting, Leading NY Doctor Says COVID-19: New Wave With 'Worst Version' Of Omicron Starting, Leading NY Doctor Says
Covid-19: New Wave With 'Worst Version' Of Omicron Starting, Leading NY Doctor Says A new COVID-19 wave with the strongest strain of the Omicron variant appears to have started in New York, one of NYC's top epidemiologists in the city is saying. Dr. Jay Varma, who was former Mayor Bill de Blasio's top public health advisor during the pandemic, said the infection rate appears to have stabilized at a high level rather than subsiding as summer starts to get into full swing. "This is likely the beginning of a BA.5 wave," Varma stated in a Tweet.  "Reported cases are at a high plateau, which means actual transmission is very high when you account for the &g…

SHARE

by Joe Lombardi
Business
National Recall Issued For Rainbox Sprinkles Products National Recall Issued For Rainbox Sprinkles Products
National Recall Issued For Rainbox Sprinkles Products A popular rainbow sprinkle product is being recalled, according to federal health officials. Illinois-based Wilton Industries initiated a voluntary recall of certain lots of Rainbow Chip Crunch Sprinkles And Rainbow Sprinkles Mix that may contain milk and could still be on store shelves, the US Food and Drug Administration (FDA) issued an alert on Monday, June 6. Rainbow Chip Crunch SprinklesFDA According to the FDA, the undeclared allergen is not declared on the product label after the issue was discovered earlier this month. Recalled items include: Rainbow Chip Crunch Sprinkles wi…

SHARE

by Zak Failla
News
COVID-19: FDA Expands Eligibility For Pfizer Booster To Children 5 Through 11 COVID-19: FDA Expands Eligibility For Pfizer Booster To Children 5 Through 11
Covid-19: FDA Expands Eligibility For Pfizer Booster To Children 5 Through 11 Federal health officials have granted emergency use authorization for a booster dose of the Pfizer-BioNTech COVID-19 vaccine in children. On Tuesday, May 17, the US Food and Drug Administration (FDA) announced that it is expanding eligibility for boosters to include children between the ages of 5 and 11 years old. That age group will be permitted to receive their booster shot five months after completing their initial COVID-19 vaccination series, officials said. FDA Commissioner Robert Califf said that while data shows COVID-19 is less severe in children, the vaccine and boosters can help …

SHARE

by Zak Failla
Business
Allergy Alert Issued For Planet Oat Non-Dairy Frozen Dessert Allergy Alert Issued For Planet Oat Non-Dairy Frozen Dessert
Allergy Alert Issued For Planet Oat Non-Dairy Frozen Dessert Sweet lovers may want to check their freezer after an allergy alert was issued for a frozen dessert product. Massachusetts-based HP Hood LLC is recalling nearly 5,000 cases of its Planet Oat non-dairy frozen dessert products over a possible undeclared peanut contamination, according to the FDA. The recall is specifically for the chocolate chip cookie dough and chocolate peanut butter swirl flavors with a best by date of 12/17/22. They were sold at stores across the United States. So far, no illnesses have been reported. The recall was issued after the company discovered that some of its…

SHARE

by Michael Mashburn
Business
Concerns Increase As US Baby Formula Shortage Worsens Concerns Increase As US Baby Formula Shortage Worsens
Concerns Increase As US Baby Formula Shortage Worsens The months-long baby formula shortage that has plagued parents and retailers across the country is getting worse, according to reports. In the first half of 2021, the out-of-stock baby formula hovered below 10 percent in the first half of 2021, according to Datasembly, though that number has jumped above 30 percent between November 2021 and April 2022. According to reports, that rate has increased above 40 percent in certain states, with some completely selling out of formula during the week of Sunday, April 24. Original story - Parents, Retailers Deal With National Baby Formula Shortag…

SHARE

by Zak Failla
Business
Recall Issued For Popular Brand Of Salad Dressing Recall Issued For Popular Brand Of Salad Dressing
Recall Issued For Popular Brand Of Salad Dressing A popular brand of salad dressing is being recalled. Van Law Food Products Inc of Fullerton, California is issuing the voluntary recall of Whole Foods Market 365 Organic Creamy Caesar Dressing because it may contain undeclared Soy and Wheat allergens, according to an announcement by the FDA. People who have an allergy or severe sensitivity to soy or wheat run the risk of serious or life-threatening allergic reaction if they consume these products. Whole Foods Market 365 Organic Creamy Caesar Dressing, with UPC code 99482-49028 is packed in 12-ounce glass bottles with a "Best" by date of 11…

SHARE

by Joe Lombardi
Business
Recall Issued For Popular Brand Of Cheese-Flavored Crackers Recall Issued For Popular Brand Of Cheese-Flavored Crackers
Recall Issued For Popular Brand Of Cheese-Flavored Crackers A popular brand of cheese-flavored crackers has been recalled. B&G Foods announced on Saturday, April 2 that it is voluntarily recalling 1,855 cases of a single date code of 6-ounce Back to Nature Cheddalicious cheese-flavored crackers, with a “best by” date of SEP 05 2022. (The “best by” date is located on the top of the box.) The recall comes after the FDA announced that the company learned that a limited number of the cracker boxes were inadvertently filled with foil wrapped pouches of animal shaped crackers, which contain egg and milk, allergens that are not declared on the box…

SHARE

by Joe Lombardi
News
COVID-19: Don't Use This Specific At-Home Test, FDA Warns COVID-19: Don't Use This Specific At-Home Test, FDA Warns
Covid-19: Don't Use This Specific At-Home Test, FDA Warns Federal health officials are cautioning Americans not to use a specific at-home rapid COVID-19 test that is being distributed but has yet to be authorized. The US Food and Drug Administration (FDA) issued an alert to advise that people should not use the ACON Laboratories test “Flowflex SARS-CoV-2 Antigen Rapid Test (Self Testing” that is packaged in a dark blue box (see above). Officials said that the test has not been authorized, cleared, or approved by the FDA for distribution or use in the United States, and the agency is concerned about the risk of false results from those using it. T…

SHARE

by Zak Failla
News
Deodorants Recalled Due To Unexpected Levels Of Cancer-Causing Chemical Deodorants Recalled Due To Unexpected Levels Of Cancer-Causing Chemical
Deodorants Recalled Due To Unexpected Levels Of Cancer-Causing Chemical A company has recalled some of its deodorant products due to unexpected levels of a carcinogen.  TCP HOT Acquisition LLC dba HRB Brands recalled "Sure" and "Brut" branded aerosol spray deodorants with expiration dates on or before August 2023, according to an announcement on Wednesday, Feb. 16. The company said the products contain unexpected levels of benzene, and that this was caused by the propellant that sprays the product from the can.  The announcement said the following products are included in the recall: Recalled productsFDA "Exposure to benzene can occur by inhalation, orall…

SHARE

by Nicole Valinote
News
COVID-19: US Sees Record 1.35M Cases In A Day, But Expert Says That Doesn't Tell Whole Story COVID-19: US Sees Record 1.35M Cases In A Day, But Expert Says That Doesn't Tell Whole Story
Covid-19: US Sees Record 1.35M Cases In A Day, But Expert Says That Doesn't Tell Whole Story Fueled by the highly contagious Omicron variant, the United States reported a record-breaking 1.35 million COVID-19 infections in a day on Monday, Jan. 10.  But that may not even be close to the actual number of cases. "We're probably only diagnosing somewhere between one in five and one in 10 actual infections," Former FDA Commissioner Dr. Scott Gottlieb said Sunday, Jan. 9 on CBS-TV. Gottlieb added that there are "probably a lot of people walking around with asymptomatic infection who don't know it, but are spreading it." That scenario could cause staffing issues for hospitals, and…

SHARE

by Joe Lombardi
News
COVID-19: Wave Of Omicron Cases In US May Be At Turning Point, Virus Expert Says COVID-19: Wave Of Omicron Cases In US May Be At Turning Point, Virus Expert Says
Covid-19: Wave Of Omicron Cases In US May Be At Turning Point, Virus Expert Says The wave of COVID-19 cases in the United States triggered by the highly contagious Omicron variant may be at a turning point, an infectious disease expert says. Former FDA commissioner Dr. Scott Gottlieb says parts of the nation may be about to pass the peak phase of the outbreak, while other regions will likely soon be hit hard. "f you look what's happening across the East Coast right now in New York City, Washington, DC, Maryland, probably Florida as well have already peaked, maybe Delaware and Rhode Island," Gottlieb said Sunday, Jan. 9 on CBS-TV's "Face the Nation." "You start to see t…

SHARE

by Joe Lombardi