Recalls

The products have been found to contain undeclared diclofenac and dexamethasone from FDA laboratory analysis. 

Diclofenac is a non-steroidal anti-inflammatory drug (commonly referred to as NSAIDs). NSAIDs may cause increased risk of cardiovascular events, such as heart attack and stroke, as well as serious gastrointestinal damage, including bleeding, ulceration, and fatal perforation of the stomach and intestines. This hidden drug ingredient may also interact with other medications and significantly increase the risk of adverse events, particularly when consumers use multiple NSAID-containing products.

Dexamethasone is a corticosteroid commonly used to treat inflammatory conditions. Corticosteroid use can impair a person’s ability to fight infections and can cause high blood sugar levels, muscle injuries and psychiatric problems. When corticosteroids are taken for a prolonged period, or at high doses, they can suppress the adrenal gland. Only licensed health care professionals can evaluate patients for the risk or existence of adrenal suppression. In addition, the undeclared dexamethasone in Notoginseng Formula Special Gout Granule may cause serious side effects when combined with other medications.

Notoginseng Formula Special Gout Granule was distributed Nationwide to via retail and ecommerce platforms including Amazon, Shopify, and Ebay, as well as at 8th Avenue Pharmacy location in Brooklyn, New York.

The product recall includes all lots within expiry of Notoginseng Gout Formula granule distributed by 8th Avenue Pharmacy. The product is a tea that is marketed as a gout treatment and is packaged in an orange and white box containing 10 tea packs. The product can be identified by UPC 6952115888087.

To date, 8th Avenue Pharmacy has not received any reports of adverse events related to this recall.

Consumers taking Notoginseng Formula Special Gout Granule should immediately consult their health care professional to safely discontinue use of this product. The risks of withdrawal from corticosteroids should be assessed by a health care professional. Abrupt discontinuation can cause withdrawal symptoms.

Consumers/distributors/retailers that have Notoginseng Formula Special Gout Granule can return to place of purchase or discard it.

Consumers with questions regarding this recall can contact 8th Avenue Pharmacy by phone (347-893-4227) or email (8avepharmacy@gmail.com) between 9AM to 5PM Eastern standard time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Complete and submit the report Online: www.fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

The two recalled spinach items were distributed to retailers in seven states including AL, FL, GA, NC, SC, TN and VA.

Fresh Express Limited Product Recall December 15, 2023

Product codes are located on the front of the packages below the use-by dates. Photos are provided for ease of identifying the products.
To date no illnesses are reported in connection with the recall and no other Fresh Express products are being recalled.

The recall was initiated after routine sampling conducted by the Florida Department of Agriculture yielded a positive result for Listeria monocytogenes in a single randomly selected package of spinach. Fresh Express immediately notified affected retailers and instructed them to remove the recalled items from store shelves and all inventories.

In the event consumers have the recalled products in their refrigerators, they should be discarded and not consumed. To obtain a refund or for more information, consumers may call the Fresh Express Consumer Response Center at (800) 242-5472 between the hours of 8 a.m. to 7 p.m. Eastern Time. Refunds are also available where purchased.

The RTE chicken fried rice product was produced on November 10, 2023. The following product is subject to recall [view labels]:

• 12-oz. trays containing Freshness Guaranteed brand “CHICKEN FRIED RICE DICED CHICKEN MEAT WITH VEGETABLES AND RICE IN A SAVORY SOY SAUCE” with lot code WK10CFR and a best if used by date of 11/10/2024 represented on the label.

The products subject to recall bear establishment number “EST. P-31993” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered by FSIS during review of testing results, which showed the product tested positive for L. monocytogenes.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. 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. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media with questions regarding the recall can contact Bob Cocat, Chief Operating Officer of Garland Ventures, at 972-485-8878 or bobcocat@ballyplus.com. Consumers with questions can contact Evelyn Tsai or Phoebe Hsu, Account Managers at Garland Ventures, at 972-485-8878, evelyntsai@ballyplus.com or phoebehsu@ballyplus.com.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

All GHGA fresh-cut fruit products associated with the recalled whole cantaloupe associated with the outbreak have expired, however consumers who have purchased these items and may have frozen them for later use are urged not to consume the products and to dispose of them immediately or return the items to their local store for a full refund.

As of November 29, there have been no illnesses reported related to GHGA fresh-cut products. According to Centers for Disease Control and Prevention (CDC), several illnesses have been reported to date in connection with the whole cantaloupe recalled by Sofia Produce, LLC dba Trufresh, however, as of November 29, no illnesses have been confirmed to be associated with GHGA products.

The fresh-cut fruit products containing recalled cantaloupe were distributed to Kroger stores in Alabama and Georgia, Sprouts stores in Alabama, Georgia, North Carolina and South Carolina, and Trader Joe’s retail stores in Alabama, Florida, Georgia, South Carolina, and Tennessee. The products are packaged in clear square or round plastic containers, marked with a “sell by” date and a lot code on the label. All pictures of products can be found on the link hyperlinked on the company name. 

Voluntarily recalled items include the specific products, lot codes, and expiration dates below. No other products are affected.

Products Table - (PDF-194KB)

Consumers who have questions or would like to report adverse reactions should contact customer service at 888.449.9386 Monday through Friday, 8 AM to 5 PM PT.

This voluntary recall is isolated to 3 batches of Burn Boot Camp Afterburn Grass-Fed Whey Protein Bars (60 grams) Triple Chocolate Almond flavor products manufactured by Doctors Scientific Organica. This product was distributed through Burn Bootcamp retail locations, as well as online through its website to locations throughout the U.S. This recall does not involve any other products, including other varieties or flavors of protein bars.

While no illnesses or injuries have been reported, we are taking this action out of an abundance of caution after consumers contacted Burn Boot Camp about this issue.

Burn Boot Camp Afterburn Grass-Fed Whey Protein Bars (60 grams)
Triple Chocolate Almond flavor products 
Lot Numbers:
181, 184 and 187

Consumers who have purchased Burn Boot Camp Afterburn Grass-Fed Whey Protein Bars (60 grams) Triple Chocolate Almond flavor products with lot codes 181, 184 and 187 should not consume the product and should return the product to the location where it was purchased or destroy it themselves. Lot numbers are printed on the back of the foil for each bar, as well as on the bottom of each cardboard case.

We are working with the U.S. Food & Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.

The quality, safety and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to our consumers and retail customers.

The recalled fruit was distributed nationwide and sold at retail stores as individual pieces of fruit bearing PLU stickers (see photos) or in consumer packaging (also shown in the attached photos) AND sold at retail between May 1 and November 15, 2022 and between May 1 and November 15, 2023.

This recall includes only conventionally grown fruit - no organic fruit is being recalled. Peaches, plums, and nectarines currently available for sale at retail stores are not included in this recall.
The recalled peaches have been linked to an outbreak of Listeriosis that has resulted in eleven illnesses.

Consumers: Although the recalled fruit is no longer available in retail stores, consumers may have frozen the recalled fruit at home for later use. Consumers are urged to check their freezers for the recalled fruit, not consume it, and discard it. Consumers with further questions can contact the company’s consumer information desk at 844-483-3867, Monday-Friday, 8:00 a.m. - 8:00 p.m. Eastern Time.

The recalled product was sold in the seafood department of Whole Foods Market stores nationwide from August 25, 2023 through November 15, 2023. This product was sold from the seafood service case wrapped in paper or prepackaged in clear trays displaying PLU 56228:

Only the Farm Raised Lightly Seasoned Atlantic Salmon Burgers with the PLU code and sell by dates listed above are impacted.

The problem was discovered after a vendor reported visible sesame seeds present on the product. An investigation is currently under way to discover the cause. No illnesses have been reported to date.

Consumers with an allergy or sensitivity to sesame or milk should not consume the product. Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with any questions may contact Raw SeaFoods, Inc. at 508-673-0111 Monday - Friday between the hours of 8am and 5pm EST.

Raw SeaFoods, Inc. is taking the necessary steps to address this issue and apologizes for any inconvenience caused. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
 

Consumers would have been able to purchase them as early as September 13, 2023. The product covered by this recall was distributed to retail stores in the following states, as well as e-commerce customers: Alabama, Arkansas, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Nebraska, New Hampshire, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Texas, Virginia, West Virginia and Wisconsin.

No other Off The Eaten Path products, flavors, sizes or variety packs are recalled.

No allergic reactions related to this matter have been reported to date. If consumers have an allergy or severe sensitivity to milk, they are encouraged not to consume the product and discard it immediately. Frito-Lay has informed the FDA of this action.

Consumers with the product described below can contact Off The Eaten Path Consumer Relations at 1-844-683-7284 (9 a.m. – 4:30 p.m. CST, Monday-Friday).
The specific recalled product information is listed below:

The affected sandwiches were distributed from October 20, 2023 and November 3, 2023, in the states of: Alabama, Connecticut, Washington, D.C., Delaware, Florida, Georgia, Kentucky, Maryland, Michigan, North Carolina, Ohio, Pennsylvania, Tennessee, Virginia, and West Virginia.

To date, no illnesses related to this product have been reported. No other products distributed by Hearn Kirkwood are being recalled. Hearn Kirkwood is working collaboratively with the U.S. Food and Drug Administration on this recall.

The recall was initiated after one of our firm’s ingredients suppliers failed to notify them the ingredient formulation had changed. This led to products being sent to customers without properly identifying the allergens of soy and milk.

Hearn Kirkwood takes the safety and integrity of the products it distributes seriously. Hearn Kirkwood regrets any inconvenience and concern this recall may cause. Customers with allergies or sensitivities to soy or milk should discard the product. Customers who have any questions about the recall may contact: RetailSalesDistribution@CoastalSunbelt.com or call 410-799-9900. 9:00 AM to 4:30 PM EST.