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November 06,2026 – East Windsor, New Jersey, Eugia US LLC (f/k/a Auro Medics Pharma LLC) is voluntarily recalling lot number 3VM26026A of Vancomycin Hydrochloride for Injection USP 1.25g/Vial-30mL (Single Dose Vial) to the hospital/healthcare facility/user level due to the presence of particulate matter identified as a glass particle inside the vial. Risk Statement: There is a reasonable probability that use of product containing glass particulates can cause serious adverse health consequences such as blockage and clotting in blood vessels, which can cut off blood flow to vital organs, lead to a life-threatening blood clot in the lungs (pulmonary embolism) and cause permanent organ damage or death. Additionally, these particles may cause local vein irritation, inflammatory reaction, aggravation of preexisting infections, and allergic reactions. Greater susceptibility may exist in neonates, infants and patients with compromised organ function. To date, Eugia US LLC has not received any reports of adverse events related to this recall. Vancomycin hydrochloride for injection is a glycopeptide antibacterial indicated in adult and pediatric patients (Neonates and Older) for the treatment of Septicaemia, Infective Endocarditis, Skin and Skin Structure Infections, Bone Infections and Lower Respiratory Tract Infections. The recalled product is packaged in 30 mL vial and packed as 10 (vials) X 10 (Printed cartons) X 01 (Shipper) with NDC code as 55150-471-01. The product can be identified by product name on carton (NDC 55150-471-10) and vial (NDC 55150-471-01) label and with lot number 3VM26026A and Exp. JUL 2028 Eugia US LLC shipped the entire lot to wholesalers nationwide from September 2, 2026, through September 15, 2026. The Company is notifying its distributors and customers by recall letters and is arranging for return/replacement of all recalled products. Wholesalers/hospitals/pharmacies, institutions, and doctors with existing inventory of the recalled product lot should discontinue use and quarantine the product immediately. If you have further distributed the recalled product lot, please notify your accounts and or any additional locations which may have received the recalled product. Hospitals and institutions should inform Healthcare professionals in your organization of this recall. Consumers with medical questions regarding this recall or reporting an adverse event can contact Eugia US LLC from 8:00 am to 5:00 p.m. (EST) Monday to Friday at: 1-866-850-2876 Option 2 [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 drug product. If you have any general questions regarding the return of this product, please contact Qualanex at 1-800-505-9291 or email [email protected] (live calls received 7:00 am to 4:00 pm M-F CST). 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 is being conducted with the knowledge of the U.S. Food and Drug Administration.

November 7, 2026, Fresh & Ready Foods LLC of Renton, WA is recalling 2,414 of Fresh To You Sausage, Egg & Cheese Biscuit Sandwiches (4.6 oz) 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 Fresh To You Sausage, Egg & Cheese Biscuit Sandwiches were produced at a Fresh & Ready facility in Renton, Washington and was distributed in Oregon and Washington to employee break rooms, refrigerated vending, and cafeterias between October 25 and November 4, 2026. This recall is in connection with a recall initiated by CH Guenther & Son for certain biscuit products that may be contaminated with Listeria monocytogenes. Fresh & Ready Foods used the affected biscuit as an ingredient only in the specific product listed below. PRODUCT | SKU & UPC | USE BY / GOOD THRU DATES | WHERE DATE CAN BE FOUND ; Fresh to You Sausage, Egg & Cheese Biscuit Sandwich.4.6 oz packaged in clear plastic film | SKU 3100048 UPC 8 405493 0168 4 | Fresh Thru: 11/07-11/19 | Front label No other Fresh To You or Fresh & Ready Foods products, production dates, or products manufactured at other Fresh & Ready facilities are impacted. No illnesses have been reported to date. Consumers who have purchased the affected product are urged not to consume the product and discard any remaining product immediately. Consumers with questions or who would like to request a full refund may contact Fresh & Ready Foods by email at [email protected] or by calling 1-855-424-8390, Monday through Friday, 8:00 a.m. to 6:00 p.m. ET.

This recall involves Arlopu Slide Playsets with model numbers KT-CS17 and LY-31. The plastic playsets are designed for indoor or outdoor use and contain multiple activity components, including a slide and a basketball hoop. The playsets are available in tan, red, blue, yellow, gray and green. Model number KT-CS17 is printed on a label located on the underside of the elevated platform of the playset. Model LY-31 is printed on a label located on the upper back panel behind the slide of the playset.

This recall involves the SuperFast Sterilizer Dryer, a countertop appliance that uses a push-button control to sterilize and dry baby bottles, breast pump parts and accessories in ten minutes. The recalled units have model numbers BRZ0083, BRZ0154 and BRZ0156. The model number is printed on the product label located on the bottom of the unit.

This recall involves lithium-ion rechargeable battery packs intended for use with Bose S1 Pro and S1 Pro+ Portable Bluetooth Speaker Systems. The serial number of the battery packs included in this recall begins with any one of the following six digits: 083723, 078352, 084105, 078591, 078592, 084106, or 086409. The 17-digit serial number for the battery pack is printed on a label placed at the bottom of the battery pack. The affected battery packs were sold with S1 Pro and S1 Pro+ Portable Bluetooth Speaker Systems and sold separately as accessories or replacement parts.

This recall includes X-Dream, X-Dream Total Dry, X-All Mountain Hammer and X-All Mountain Adze. These products are designed for vertical ice climbing. The batch number is located on the side of the shaft. “CAMP” is written in white lettering on the ice axes shaft. The recalled nut and bolt kit were also sold as an accessory item as model number 3641. Recalled Models and Batches • X-Dream (model: 3570): Batches 10/24, 07/25, 10/25, 12/25 • X-Dream Total Dry (model: 3609): Batches 10/24, 07/25, 11/25 • X-All Mountain Hammer (model: 3630): Batches 10/24, 09/25 • X-All Mountain Adze (model: 3631): Batches 10/24, 09/25 • Accessory Kit (nut and bolt) (model: 3641)

This recall involves Gourmia 9-SliceDigitalAir Fryer Ovens with model number GTF7530, and UPC Code 810002862779. The recalled ovens are stainless steel and have two spring-loaded glass front French doors with metal handles. The Ovens can be identified with model and UPC codes on packaging. The Model number GTF7530 and codes 3021 to 0126 can also be found on a label on back of the unit.

This recall involves HAUOM-branded Eight-drawer dressers. The wooden black dressers measure about 27.6 inches wide, 15.8 inches long, 59.1 inches tall, and weigh about 112.4 pounds. "SKU: AJ_DJ504298_1" is printed on the product packaging.

This recall involves X-VESOLJE Nursing Pillows, model number NP001. The nursing pillows are C-shaped and sold in white with leaves pattern, dark brown with multicolored feather pattern and multicolored puzzle piece pattern. There are no markings or labels on the product.

This recall involves Little Giant ladders with Rapid Locks. Rapid Locks are designed to insert into ladder rungs for the purpose of adjusting the ladder’s height. Rapid Locks are black or orange and are located on each ladder leg. The affected models are Adjustable Fortress 2.0, Conquest 2.0, Dark Horse 2.0, Epic, King Kombo XT, Leveler, MegaLite, MegaLite+, Multi, Quantum and Vector. The brand name Little Giant and the model name are located on the side of the ladder. Only ladders without an orange rectangular “QC” sticker on the rail above one of the Rapid Locks are included in this recall.

Coral Gables, FL - Snack Right Super Foods, Inc., doing business as Brad's Raw Chips, is recalling certain Brad's Plant Based Crunchy Kale (2 oz) and Brad's Veggie Chips Kale (3 oz) products because they may contain thallium. Thallium (Tl) is a naturally occurring metal found in the soil and in sulfur-based minerals. It can be taken up by plants and vegetables, particularly those in the Brassicaceous family (i.e., cabbage, radish). Acute or chronic exposure to thallium at relatively high levels can result in serious adverse health effects, including gastroenteritis, damage to peripheral nerves, and alopecia (hair loss). The products were distributed nationwide through KeHE Distributors and United Natural Foods, Inc. (UNFI), and sold directly to five individual consumers. Approximately 25,000 bags (about 2,097 cases) of the recalled products are estimated to be in commerce. Distribution occurred between October 2025 and December 2025. The recall includes the following Brad's Plant Based products, all in bags, distributed under the brand name Brad's Plant Based, with the lot numbers and Best By dates listed below: Brad's Crunchy Kale, Original, 2 oz (57g) bag, UPC 813104021679, Lots 33525-1, 33525-2 and 33525-3 (Best By February 1, 2027), Lot 34525-1 (Best By February 11, 2027) and Lot 35125-2 (Best By February 17, 2027) Brad's Crunchy Kale, Cheeze It Up, 2 oz (57g) bag, UPC 813104021877, Lot 35025-3 (Best By February 16, 2027) Brad's Crunchy Kale, Radical Ranch, 2 oz (57g) bag, UPC 813104020726, Lot 29425-1 (Best By December 21, 2026) Brad's Veggie Chips Kale, 3 oz (85g) bag, UPC 854615002054, Lot 33225-3 (Best By January 28, 2027), Lot 33325-2 (Best By January 29, 2027), Lot 33425-1 (Best By January 30, 2027) and Lot 33525-1 (Best By February 1, 2027) In May 2026, the California Department of Public Health (CDPH) advised consumers not to eat certain Brad's Plant Based products after it investigated an inquiry from one individual with elevated thallium levels. CDPH collected samples at retail stores in the Sacramento area, and laboratory testing found elevated thallium levels in multiple varieties. The recall was initiated after the U.S. Food and Drug Administration (FDA) advised the firm of thallium in tested products. Brassica crops such as kale are known to accumulate certain elements from soil. The manufacturing process did not introduce the contaminant; however, the dehydration process removes approximately 85 to 90 percent of the product's water, which concentrates elements already present in the fresh kale. Consumers who have purchased any of the products listed above should stop consuming them immediately and discard the product. Refunds are not being offered, and the product should not be returned to the place of purchase. Consumers with questions may contact Alexa Olvera at Snack Right Super Foods, Inc. by email at [email protected], Monday through Friday, 10:00 a.m. to 4:00 p.m. Eastern Time. Consumers can expect a response within one business day. Consumers who believe they may have experienced adverse health effects from consumption of these products should contact their health care provider. This voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Once Upon a Farm (Berkeley, CA) is recalling all lots and varieties of fruit-flavored Tractor Wheel Organic Toddler Soft-Baked bars due to reports that the composition of the Tractor Wheel toddler snack can rapidly hydrate into a dense, dry, and sticky mass upon contact with saliva and during chewing, which can result in a potential choking hazard for toddlers for ages 1.5-2.5 years old. The Tractor Wheels were distributed nationwide, including Puerto Rico, and reached consumers via online sales and retail stores. This recall covers all lot codes currently available in distribution, including expired products which may be on consumers' shelves. Applicable unexpired Best If Used by Dates are 10/30/2026 to 8/26/2027. Recalled products can be identified as follows: Tractor Wheels – Strawberry, Pumpkin & Beet 5 count - Net Wt. 3.35 oz (95g) - UPC 81000351261 10 count - Net Wt. 6.7 oz (190 g) - UPC 810003512932 Tractor Wheels – Apple, Sweet Potato & Spinach 5 count - Net Wt. 3.35 oz (95g) - UPC 81000351260 10 count - Net Wt. 6.7 oz (190 g) - UPC 810003512840 Tractor Wheels – Banana, Pumpkin & Cauliflower 5 count - Net Wt. 3.35 oz (95g) - UPC 81000351262 Tractor Wheels (Variety Pack) – Strawberry, Pumpkin & Beet/Apple, Sweet Potato & Spinach 20 count – (10) Apple, (10) Strawberry - Net Wt. 13.4 oz (380g) - UPC 810003512918 TW 30 Ct Variety Pack – Stawberry, Pumpkin & Beet (10ct)/Apple, Sweet Potato & Spinach (10ct), Banana, Pumpkin & Cauliflower (10ct) 30 count - Net Wt. 20.1 oz (570g) - UPC 810003512925 Organic Baby & Toddler Snack Sampler Packs – Online Only – containing 5 count cartons of Tractor Wheels along with other Baby and Toddler Snack products Organic Baby & Toddler Snack Sampler 9 count - Contains 3 - 5 count cartons of tractor wheels all three flavors - Case 10810003513670 Organic Baby & Toddler Snack Sampler 12 count - Contains 3 - 5 count cartons of tractor wheels all three flavors - Case 10810003513694 Organic Ultimate Snack Sampler 15 count - Contains 3 - 5 count cartons of tractor wheels all three flavors - Case 10810003513687 The decision to recall these products was based on three consumer complaints that were reported to FDA for choking. No injuries have been reported to date. We are working with the U.S. Food & Drug Administration (FDA) to make sure affected products are removed as the company works on reformulating and families have the information they need. Consumers who have purchased this recalled Once Upon a Farm Tractor Wheels product should not open the package or consume the products. Instead, they should return the product to the location of purchase for a full refund or contact [email protected]. Consumers with questions should contact the company at [email protected] or call 1-888-983-1606 to contact our customer care team Monday – Friday: 6:00 am – 4:30 pm, PST and Saturday: 8:00 am – 11:00 am, PST. We are sorry for the worry and disruption this has caused parents, caregivers, and our retail partners. Link FDA Advisory

“Firm press was updated on 10/30/2026 to reflect nationwide product distribution rather than to select states.” Vitality Works Inc. of Albuquerque, New Mexico, is recalling one lot (lot number 2025-26227) of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules 120 count because it has the potential to be contaminated with Salmonella, an organism that 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 may experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organisms entering the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis. The recalled product was available for purchase from November 24, 2025, through October 20, 2026, both online through Amazon.com and at Whole Foods Market stores nationwide. The product is packaged in white plastic bottles labeled as 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha 120 count, with UPC 9948252099. The product can be identified by lot number 2025-26227 and expiration date 10/13/2028, both printed on the bottom of the bottle. No illnesses have been reported to date. The potential contamination was identified through routine sampling of a single retail unit. Customers who have the recalled product should not consume it. Discard the recalled product and do not return it to the store. Refunds are available at any Whole Foods Market store. Consumers with questions may contact Vitality Works Inc. at (505) 268-9950. Business hours are Monday-Friday 8:00 AM – 5:00 PM Mountain Time.

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

El Ruisenor De Mexico, Inc. — Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

El Ruisenor De Mexico, Inc. — Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

El Ruisenor De Mexico, Inc. — Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

El Ruisenor De Mexico, Inc. — Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

El Ruisenor De Mexico, Inc. — Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.