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October 24, 2026, Tonight We Ride, LLC of Lakeville, Minnesota is voluntarily recalling all lots of Ultimate Forza Male Supplement capsules to the consumer level because it has been found to contain undeclared Sildenafil, Tadalafil, and Dapoxetine. The presence of Sildenafil, Tadalafil, and Dapoxetine in this product renders them unapproved drugs for which the safety and efficacy have not been established. Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Dapoxetine is an active ingredient not approved by the U.S. FDA and therefore its safety or efficacy has not been established. Chemically, dapoxetine belongs to a class of drugs known as selective serotonin reuptake inhibitors (SSRIs) used to treat depression. Consumption has been shown to increase the risk of suicidal thinking and behavior in children, adolescents, and young adults. Ultimate Forza products subject to the recall include the Ultimate Forza Multi-Capsule/Box (Item #810208, UPC 868592000002) and the Ultimate Forza Single Pack (Item #810222, UPC 868592000040). These items were distributed through certain independently owned and operated GNC franchise locations in the United States from 2017 to October 1, 2026. The products were not sold through GNC corporate stores. Ultimate Forza Male Supplement capsules are marketed as male performance dietary supplements. The Multi-Capsule/Box configuration contains ten blue hard-shell capsules, and the Single Pack contains one capsule. No adverse events or complaints have been reported to date. The recall was initiated after GNC's third-party product testing identified undeclared sildenafil, tadalafil, and dapoxetine. Sales were stopped, affected products were quarantined at franchise locations, and customers were notified to discontinue use and return remaining product. Consumers should stop using Ultimate Forza Male Supplement immediately. Consumers may return unopened or partially used product to a GNC store for a full refund. A receipt or the phone number or email address associated with the loyalty account used for the purchase should be provided so the purchase can be verified. Consumers with questions may contact GNC Customer Service at 1-877-462-4700 or [email protected]. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this 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.

This recall involves Bamamon LED Projecting Finger Light toys which contain three button cells batteries. The finger lights come in 32 pieces in a box in red, orange, blue, black, purple, clear, green and yellow. The finger lights project eight space themed patterns such as astronauts, rockets, UFO, galaxy and solar systems printed on labels located on the front of the package.

This recall involves Costway high chairs designed to convert into a table and chair set. They were available in several color combinations, including purple and white, red and white, blue and white, and brown and white. There is no tracking information located on the products.

This recall involves CIYTI Light-Up Princess Costumes. The costumes include a blue dress with a crown and wand that light up, and a remote control. The crowns, scepters, and remote controls contain button batteries. There are no markings on the product. The package has "CIYTI" on the front.

This recall involves Luminaires with certain adjustable tilt mounting arms manufactured between August 2019 to July 2020 and August 2024 to April 2026: AASP, AARP, AAWB, and AAWSC. The adjustable tilt arm mounts the RSX luminaire to a square pole, round pole, wall bracket or wall bracket with surface mount conduit. The arm mount allows the luminaire to be tilted from 0 degrees to 90 degrees above horizontal. Consumers should contact Lithonia Lighting to confirm their Luminaire with adjustable tilt mounting arms are included in the recall.

This recall involves VQQQ-branded natural gas patio heaters, models VQQQ-A1 and VQQQ-001. They have a bronze pole with a round base and a silver mushroom-shaped top with an adjustable height of 55 inches to 78 inches. A 24-foot-long gray gas hose is attached to the heater's base. The brand and model numbers are printed on the product's purchase receipt.

The U.S. Consumer Product Safety Commission (CPSC) is warning consumers to stop using PowRyte pressure washers immediately. The pressure washers lack an integrated immersion protection device on or near the power plug, also known as a Ground-Fault Circuit-Interrupter (GFCI), posing a risk of death or serious injury due to electrocution and shock. Powell Works, Inc. of China has not responded to requests for a recall. CPSC urges consumers to stop using the pressure washers immediately, and destroy them by unplugging, cutting the power cord, and disposing of them. Do not sell or give away these hazardous pressure washers. These pressure washers are sold in green with black, with a variety of accessories including a hose, multiple quick-connect nozzles and a foam cannon.

The U.S. Consumer Product Safety Commission (CPSC) is warning consumers to stop using Reliancer bed rails immediately because they violate the mandatory standard for adult portable bed rails, posing a deadly risk of entrapment and asphyxiation. When the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. In addition, the bed rails do not meet the structural stability or retention strap requirements, posing a fall hazard. In addition, the bed rails do not bear the required hazard warning labels. CPSC urges consumers to stop using the bed rails immediately and dispose of them. Do not sell or give away these hazardous products. CPSC issued a Notice of Violation to the retailer, Ningbo Beitao Trading Co., Ltd., doing business as Reliancer, of China. Reliancer has not responded to CPSC requests to conduct a recall or offer a remedy for the bed rails to consumers. This warning involves Reliancer-branded adult portable bed rails. The bed rails have white tubing with black foam rubber handle grips and a black storage pocket. The bed rails measure about 26.4 inches wide by 38.6 inches tall and weigh about 5 pounds. “Reliancer” is printed on the bed rail’s storage pocket.

The U.S. Consumer Product Safety Commission (CPSC) is warning consumers to stop using Kaizou Group’s Rainbow Mystery Squishy Bun and Squeezy Dumpling toys immediately. The toys violate the mandatory safety standard for toys containing water beads , posing deadly ingestion, choking, and obstruction hazards. CPSC urges consumers to stop using the toys immediately and dispose of them. Do not sell or give away these hazardous products. CPSC issued a Notice of Violation to the distributor, Kaizou Group Inc., of Pico Rivera, California. Kaizou Group has been unresponsive to CPSC’s request to recall these squishy toys or offer a remedy to consumers. This safety warning involves Rainbow Mystery Squishy Bun Toys and Squeezy Dumpling Toys. The squishy bun toys are translucent and contain glitter and water beads. The squishy bun toys have a cartoon face and are packaged in a tan plastic container shaped like a bamboo steamer. “Rainbow MYSTERY” and “ONE SET SUGAR EDITION” are printed on the front of the removable package labeling. There are no markings on the product, other than the cartoon face. The squeezy dumpling toys are translucent and contain multicolor water beads. The toys have a cartoon face and are packaged in a tan plastic container shaped like a bamboo steamer. “SQUEEZY DUMPLINGS” is printed on the front of the removable package labeling. There are no markings on the product, other than the cartoon face.

10/22/2026, Vitamin Cottage Natural Food Markets, Inc., Lakewood, Colorado, is recalling Natural Grocers Brand Organic 2-Pound Mung Beans due to the potential presence of glass. The recall is being initiated after receiving customer complaints about sharp glass fragments in the product. Ingesting glass fragments may cause injury to the consumer, and these injuries may include damage to teeth, laceration of the mouth and throat, or perforation of the intestine. No illnesses or injuries have been reported to date. The affected lots may have shipped to Natural Grocers stores in the following states: AR, AZ, CO, IA, ID, KS, LA, MN, MO, MT, ND, NE, NM, NV, OK, OR, SD, TX, UT, WA, WI and WY. These lots began shipping on 6/10/26. The recalled Natural Grocers Brand Bulk Organic Mung Beans are packaged in 2-pound clear plastic bags with UPC 000080112600. The recall includes the following pack dates: 26-160, 26-173, 26-196, 26-224, and 26-258, which can be found in the lower left corner of the label. Consumers who purchased this product should discontinue use immediately and either discard it or return it for a full refund or credit. Consumers with questions may contact the company at 303-226-1434, Monday-Friday, 8am-5 pm (mountain time), or send email to [email protected]. This recall is being made with the knowledge of the U.S. Food and Drug Administration.

October 22, 2026 - WinCo Foods of Boise, ID is recalling the following WinCo Foods Brand Hoagie Rolls due to undeclared sesame. WinCo Foods Hoagie Rolls with UPC 2-70552-00649-2, with a net weight of 16oz(1LB) 454g, with Best By Dates of 9/10/2026 – 11/3/2026. The best by date will be formatted as “Best if used by SEP 9” printed on the bag. People who have an allergy or severe sensitivity to sesame may risk a serious or life-threatening allergic reaction if they consume this product. The recalled product was distributed to WinCo Foods retail stores in CA, ID, MT, NV, OR, UT, and WA. The recall was initiated after the manufacturer, United States Bakery, discovered the packaging did not declare sesame flour in the ingredient list and allergen statement. No illnesses have been reported. Consumers are advised not to consume the hoagie rolls if they have a sensitivity or allergy to sesame, and to return them to their nearest WinCo Foods location for a refund. Consumers with questions or concerns are welcome to contact the WinCo Foods Customer Service Desk at 1-800-824-1706, or online through the WinCo Foods Customer Service Contact Us form. This recall is being made with the knowledge of the Food and Drug Administration. Consumer Contact Information: WinCo Foods Customer Service Desk Phone number: 1-800-824-1706 Website: WinCo Foods - Contact Us Online

SWEDESBORO, N.J., (October 21, 2026) - Wedgewood Pharmacy LLC ("Wedgewood") is recalling certain compounded veterinary medications within expiry at the provider/customer level due to inconsistencies in the reliability of certain analytical testing data generated by their laboratory, potentially resulting in subpotent and/or superpotent products. The affected products were shipped between February 18, 2026 and October 6, 2026 to veterinary practices, pharmacies, and other customers nationwide in the U.S. The issue was discovered through Wedgewood’s own quality processes. A complete list of affected products (including powders, pastes, oral suspensions, injectables, ophthalmic ointments and solutions, ear solutions and suspensions, topical sprays, and gels), lot numbers, and expiration dates are available at www.wedgewood.com/recall-lookup/. The products involved are intended for companion, equine, exotic, zoo, wildlife, and aquatic animals. They are not intended for use in food-producing animals. Hazard Statement: The health risks involved with low potency can include ineffective treatment and the health risks involved with high potency can include toxicity or overdose. To date, Wedgewood has received 98 complaints, of which 7 are serious. Customers should contact their veterinarians if they have medical concerns. For customers: Wedgewood has engaged Sedgwick to support the coordination of this recall. Sedgwick is notifying affected customers via email and mail and is arranging a refund or, where possible, replacement of recalled products. Animal owners who have received affected product should stop use, retain the product, and contact Wedgewood’s recall services by phone at 866-562-5931 Monday through Friday 8am – 9pm ET and Saturday 9am to 5pm ET. For businesses: Veterinary practices, pharmacies, and other customers should immediately examine their inventory, quarantine any affected product and contact Wedgewood’s recall services by phone at 866-562-5931 Monday through Friday 8am – 9pm ET and Saturday 9am to 5pm ET. Veterinary practices or pharmacies who have further dispensed affected product should identify and notify their customers of the recall. For clinical alternatives: Wedgewood is working to help customers, veterinarians, and pet owners maintain continuity of care, including identifying clinically appropriate alternatives where available. To identify alternative treatment options, customers can contact Sedgwick by phone at 866-562-5931 Monday through Friday 8am – 9pm ET and Saturday 9am to 5pm ET. Sedgwick will refer any clinical questions to Wedgewood’s care team. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA at 1888-FDA-VETS or online at http://www.FDA.gov/reportanimalae.

ARLINGTON, VA – OCTOBER 16, 2026 – Lidl US is recalling one lot of Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces 16 FL OZ (1 PT) UPC 4 0564897 22458 Lot: 085261 Best By MAR/26/2028 because it has the potential to be contaminated with 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, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women. The recalled product was distributed between 7/19/2026 - 10/15/2026 to all Lidl US retail store locations in Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia. The recalled product can be identified as follows: Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces 16 FL OZ (1 PT) UPC 4 0564897 22458 Lot: 085261 Best By MAR/26/2028, which can be found on the bottom of the container. The recalled product is packaged in a clear plastic container with a brown lid. No illnesses have been reported to date. This recall was initiated after routine quality testing identified Listeria monocytogenes present on a lab sample. Customers should immediately discard or return the recalled product to their nearest Lidl store for a full refund (a receipt is not required for return). Customers who have questions about this recall should call the Lidl US Customer Care Hotline at (844) 747-5435, Monday – Saturday between 8 am - 8 pm ET. The health and safety of our customers is our top priority. Lidl US regrets any inconvenience related to this voluntary recall. Our Quality Assurance Department is constantly working to ensure that all products on our shelves meet the high-quality standards that we would expect when feeding our own families. We are grateful for all our Lidl US customers who choose to shop with us every day.

Krasnyi Oktyabr Inc. of Brooklyn, New York, is voluntarily recalling STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED (227g/8oz) packages, because the product has the potential to be contaminated with 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, stiffness, nausea, abdominal pain, and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. The STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED (227g/8oz) product was distributed in New York, Florida, Georgia, New Jersey, Pennsylvania and Ohio. The recalled product is identified as follows: Product Name: STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED Brand: STARFISH SEAFOODD Net Weight: 227g/8oz Storage Method: Frozen Packaging: Vacuum-sealed plastic package UPC Code: 4751048940099 Product Code: Best before: 27.11.2027 LOT: D080-148 Country of Origin: Latvia No illnesses have been reported to date in connection with this product. The potential contamination with Listeria monocytogenes was identified by sampling of the product conducted by the New York State Department of Agriculture and Markets. As a result, Krasnyi Oktyabr Inc. initiated a voluntary recall of the affected product. The company is cooperating with the New York State Department of Agriculture and Markets and the FDA regarding the recall. Krasnyi Oktyabr Inc. is a wholesale distributor and did not manufacture the recalled product. The company has notified its affected customers and requested that they immediately discontinue the sale and distribution of the recalled product, identify any remaining inventory, and notify their customers as appropriate. Consumers who have purchased the recalled STARFISH SEAFOOD PREMIUM COLD SMOKED NORWEGIAN SALMON SLICED are urged not to consume the product and to return it to the place of purchase for a full refund. Consumers with questions may contact Krasnyi Oktyabr Inc. at (718) 858-6720, Monday through Friday, from 9:00 a.m. to 5:00 p.m. Eastern Time (ET).

“This is an update to the company’s press release, previously issued on 10/15/2026, to correct the distribution pattern and serotype of E. coli” WORCESTER, NY, October 15, 2026 - Family Farmstead Dairy of Worcester, NY is recalling specific lot of cheddar cheese because it may be contaminated with Escherichia coli O26:H11 and O45:H2 (E. Coli O26:H11 and O45:H2). E. coli O26:H11 and O45:H2 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death. Product to grocers in NY, PA, NJ, CT, MD, VA, and MA. But the product may also have been distributed to other states via downstream distributors. Affected Product Product: Family Farmstead Dairy Raw Mild Cheddar Cheese Lot Code: 7/22/27 Best By Date: 7/22/27 No other Family Farmstead Dairy products are included in this recall. No illnesses or allergic reactions have been reported to date. The issue was discovered when a LFFM sample in Maryland isolated two strains of Shiga toxin-producing E. coli (STEC) in two samples of Family Farmstead A2 Raw Cheddar, 8 oz package, 7/22/27. Consumer Information Consumers who have purchased the affected product should not consume it. The product should be discarded or returned to the place of purchase for a full refund. At this time, Family Farmstead Dairy has received no reports of illness associated with the recalled product. Consumer Contact Information Consumers with questions regarding this recall may contact: Family Farmstead Dairy Phone: (607) 397-4044 Email: [email protected] 8:30am-5:00pm Easterm, Mon-Fri. "We sincerely apologize to our customers, retail partners, and consumers for the inconvenience caused by this recall. Product quality is an utmost priority here at Family Farmstead so we are committed to identifying the cause of this issue and taking all necessary corrective actions to ensure the continued safety and quality of our products." About Family Farmstead Dairy Family Farmstead Dairy is a New York-based dairy processor dedicated to producing high-quality dairy products while maintaining rigorous food safety and quality standards.