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This recall involves DREO space heaters, model number DR-HSH015. The ceramic, electric heaters are black and measure about 11.5 inches wide and 13 inches tall and include a remote control. Only units manufactured from April 2025 through January 2026 are included in this recall. The manufacture date, in YYYY/MM format, and the model number are printed on a label on the heater’s underside and “DREO” on the front of the unit.

This recall involves QZH.DUAO pajama sets. The pajama sets consist of short-sleeve tops and matching pants. They were sold in Pink Bow, Pink, Black, Light Blue, Purple, Mint Green, Hot Pink, Pink Bowknot, Blue Bowknot, Pink Strawberry and Pink Bow Flower and in sizes 4-5T through 13-14 years.

This recall involves Harkla’s children’s sensory swings. The compression swings have a blue fabric seat and come with a four-hole hook and ceiling mounting hardware for suspension, with a drop length of 18 to 24 inches. Only swings with a four-hole hook are included in this recall. SKU number LS-COMP-1BLU or LS-COMP-1BLU-SW is printed on the side of the product packaging.

This recall involves Pamag Pieeoo Mattresses. The mattresses are 8 inches thick and were sold in a twin-XL size. They have a white top and white sides with a gray curve pattern. They were sold compressed in a box. The date of manufacture and “Model: BFC8HMBYTX-US” and care instructions are printed on a sewn-in white label located on one side of the mattress.

This recall involves NTI brand residential gas boilers in the FTVN and TFTN model series, and HTP brand residential gas boilers in the EFTU model series. The NTI FTVN and TFTN series boilers are gray, while the HTP EFTU (Elite Fire Tube Ultra) boilers are black. The boilers are metal, rectangular units and have either NTI or HTP printed on the front. The model serial number can be found on the rating plate, located on the left-hand side of the boiler. The following models and serial number ranges are included in this recall:

This recall involves PILLANI-branded nursing pillows. The U-shaped nursing pillows were sold in the following colors and prints: cloud and stars, wild animal, white with leaf and feather, stars, pink with leaf, light blue, pink, light yellow, gray, light gray, beige and light green. The pillows have a smaller pillow attached atop and an adjustable waist strap. The brand name, model number NP4351 and batch numbers 202604, 202605 or 202606 are printed on an attached label.

This recall involves three RootStim Minoxidil Hair Regrowth Treatment bottles: RootStim 5% Minoxidil Foam Hair Regrowth Treatment with Rosemary and Biotin, 6 fl. oz. The Foam comes in a blue and white package, with an orange accent band or orange lettering. The package contains three 2 fl. oz. pump-foam bottles. UPC code 810169130594 is printed on a label on the bottom of the box. RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil Rosemary & Biotin, 2 fl. oz. The spray comes in a magenta box with a 2 fl. oz spray-pump bottle. UPC code 810169301005 is on a label on the bottom of box. RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil with Rosemary, 4 fl. oz. The serum comes in a blue and white package with an orange accent band containing two 2 fl. oz. amber glass bottles with black spray-pump caps. UPC code 810169301012 is on a label on the bottom of the box.

This recall involves SOOWERY 8-Drawer Fabric Dresser. The recalled dressers come in gray and black. The dressers have eight fabric drawers and the frames are made of metal. They measure 47.2 inches wide, 11.8 inches long, 35.4 inches tall and weigh 47.5 pounds. The SKU “SOO-8DD-G01” is printed on the products packaging.

SLR Food Distribution Inc. of Hicksville, New York, is voluntarily recalling Wise Wife Brand Ground Cinnamon because it has the potential to be contaminated with elevated levels of lead. Short-term exposure to very low levels of lead may not elicit any symptoms. Increased blood lead levels may be the only apparent sign of lead exposure. Additional signs and symptoms are more likely with acute exposure to higher levels of lead or chronic exposure to lead. While lead can affect nearly every bodily system, its effects depend upon the amount and duration of exposure, as well as the age and body weight of the individual. If a child is exposed to enough lead for a prolonged period of time, such as weeks to months, permanent damage to the central nervous system may occur. This can result in learning disorders, developmental defects, and other long-term health problems. Wise Wife Brand Ground Cinnamon (UPC: 0688474302754) was distributed to retail stores and grocery stores in Connecticut, Indiana, Kansas, Massachusetts, Michigan, Minnesota, North Carolina, Nebraska, New York, Ohio, Pennsylvania, Texas, Virginia, and Wisconsin between September 8, 2025, and June 28, 2026. The recalled product is packaged in a 110 g (3.88 oz) clear plastic container with a black screw-top cap. The Best Before date is 4/25/2027. The UPC 0688474302754 is printed on the back label of the product. No illnesses have been reported to date. The recall was initiated after a sample collected and analyzed by The Connecticut Agricultural Experiment Station revealed elevated levels of lead in the product. SLR Food Distribution Inc. has initiated a recall and is notifying customers to stop distribution and sale of the affected product and to remove the product from store shelves. Customers are being instructed to place any remaining inventory on hold and follow the company's recall instructions. Consumers should not consume the recalled product and should either discard it or return it to the place of purchase for a full refund. Company Contact Information Consumers with questions may contact: SLR Food Distribution Inc. 495 West John St. Hicksville, NY 11801 Phone: 1-516-437-3782 Email: [email protected] Business Hours: Monday–Friday, 9:00 a.m.–5:00 p.m. Eastern Time

Taylor Farms of Dallas, Texas is recalling H-E-B Backyard BBQ Chop Salad kit due to the potential undeclared soy and tree nuts(almonds). People who have sensitivity or allergy to soy and tree nuts(almonds) may be at risk of a serious adverse reaction if they consume this product. To this date, there have been no reported adverse reactions to this product. The recalled product was distributed to H-E-B stores located in Texas and has the Best If Used By date October 30, 2026. The recalled product is packaged in plastic bags and can be identified by the Best If Used By date and UPC code below: STORE | ITEM DESCRIPTION | BEST IF USED BY DATE | UPC ; H-E-B | Backyard BBQ Chop Salad Kit 13.4 oz | October 30, 2026 | 041220300457 Customers who purchased the products should not consume the items. Impacted products should be disposed of or returned to the store for a full refund. Customers with questions may contact Taylor Farms at (855) 455-0098 Monday through Friday between 8am and 4pm PST. Media: [email protected]

HAIFA SMOKED FISH of QUEENS NY is recalling approximately 560 lbs. of Cold Smoked Sprats, due to potential contamination with Clostridium botulinum, a bacterium which can cause life-threatening illness. Consumers are warned not to use the product even if it does not look or smell spoiled. Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention. Cold Smoked Sprats was distributed in New Jersey, New York and Pennsylvania through retail stores. The product packed loose in bulk cardboard boxes labeled Cold Smoked Sprats and shipped refrigerated. All Lots are included in the recall "No illnesses have been reported to date." FDA initiated an inspection at D&M Smoked Fish Inc., of Jamaica, NY, and the inspection revealed that the firm was producing cold-smoked sprats without required food safety controls to prevent Clostridium botulinum growth and toxin formation. Consumers who have purchased Cold Smoked Sprats are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-523-8899, between 9am and 5 pm, Eastern Standard Time. Link to FDA Advisory

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.

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