- Why it was recalled
- Undeclared soy and tree nuts (almonds)
- What to do
- Follow the company's instructions in the official FDA announcement.
Affected identifiers: STORE | ITEM DESCRIPTION | BEST IF USED BY DATE | UPC
H-E-B | Backyard BBQ Chop Salad Kit 13.4 oz | October 30, 2026 | 041220300457
Company announcement: 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… View all
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]
- Why it was recalled
- Potential contamination with Clostridium botulinum
- What to do
- Follow the company's instructions in the official FDA announcement.
Affected identifiers: Cold Smoked Sprat Fish
Company announcement: 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… View all
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
- Why it was recalled
- Product contains undeclared Sildenafil, Tadalafil, and Dapoxetine
- What to do
- Follow the company's instructions in the official FDA announcement.
Affected identifiers: Male Supplement
Company announcement: 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… View all
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.
- Why it was recalled
- None reported.
- What to do
- Consumers should stop using the toys immediately and contact Bamamon. Consumers will be asked to email a photograph showing the product being properly disposed of in the trash to [email protected].
Affected identifiers: Bamamon LED Projecting Finger Light Toys
Firm / distribution: 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… View all
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.
- Why it was recalled
- The convertible high chairs violate the mandatory safety standard for high chairs because they do not contain a passive restraint system and a child can slip through the opening between the feeding tray and seat and become entrapped or fall, posing a risk of serious injury or death.
- What to do
- Consumers should immediately stop using the recalled high chairs and contact Costway for a free replacement high chair. Consumers will be asked to provide a receipt or a photo of the product and will receive a prepaid label to return the recalled product to Costway. Upon receipt of the recalled product, Costway will ship a replacement high chair free of charge.
Affected identifiers: Costway Convertible High Chairs
Firm / distribution: 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.… View all
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.
- Why it was recalled
- The costumes violate the mandatory safety standard for toys because the button cell batteries can be accessed easily by children, posing a deadly ingestion hazard. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- What to do
- Consumers should take the princess costumes away from children immediately, stop using them and contact FoShanShiNanHaiQuNuoAiTongZhuangShangHang for a full refund. Consumers will be asked to write "RECALLED" with permanent marker on the dress, crown, wand, and remote, then throw away the toys and submit a photo of the disposed toys to [email protected]. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures.
Affected identifiers: CIYTI Light-Up Princess Costumes
Firm / distribution: 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.… View all
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.
- Why it was recalled
- The knuckle of the recalled adjustable tilt arm mountings can fail, allowing the luminaire to fall from the mounting arm, posing a risk of serious injury due to impact hazard.
- What to do
- Consumers should keep clear of the area directly beneath the Luminaire and contact Lithonia Lighting to schedule a free repair. Lithonia Lighting will arrange for a qualified professional to replace the recalled adjustable tilt arm mount with a new complete adjustable arm assembly.
Affected identifiers: Lithonia Lighting RSX Luminaires with AASP, AARP, AAWB, and AAWSC Adjustable Tilt Arm Mountings used for commercial outdoor lighting.
Firm / distribution: 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… View all
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.
- Why it was recalled
- Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards.
- What to do
- Consumers should stop using the recalled patio heaters immediately, shut the valve at the portable gas source, disconnect the gas hose and contact VQQQ for a full refund. Consumers will be asked to write in permanent marker "Recalled" on the heater's base and send a photo of the marked heater to [email protected]. Consumers should then dispose of the recalled product.
Affected identifiers: VQQQ Natural Gas Patio Heaters
Firm / distribution: 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… View all
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.
- Why it was recalled
- 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.
- What to do
- 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.
Affected identifiers: PowRyte pressure washers
Firm / distribution: 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… View all
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.
- Why it was recalled
- The recalled bed rails violate the mandatory standard for adult portable bed rails because 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, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. In addition, the bed rails do not bear the required hazard warning labels.
- What to do
- CPSC urges consumers to stop using the bed rails immediately and dispose of them. Do not sell or give away these hazardous products.
Affected identifiers: Reliancer Adult Portable Bed Rails
Firm / distribution: 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… View all
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.
- Why it was recalled
- The toys violate the mandatory safety standard for toys containing water beads , posing deadly ingestion, choking, and obstruction hazards.
- What to do
- CPSC urges consumers to stop using the toys immediately and dispose of them. Do not sell or give away these hazardous products.
Affected identifiers: Kaizou Rainbow Mystery Squishy Bun Toys, Squeezy Dumpling Toys
Firm / distribution: 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… View all
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.
- Why it was recalled
- Possible foreign material contamination with glass
- What to do
- Follow the company's instructions in the official FDA announcement.
Affected identifiers: 2 pound Mung Beans
Company announcement: 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… View all
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.
- Why it was recalled
- Undeclared sesame
- What to do
- Follow the company's instructions in the official FDA announcement.
Affected identifiers: Hoagie Rolls
Company announcement: 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… View all
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
- Why it was recalled
- Foreign object: May contain pieces of metal
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: best by Feb.10.27 — 10,392 units
Firm / distribution: Stewart's Shops Corp. — NY, VT, NH
- Why it was recalled
- Undeclared soy.
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: Best if USED BY Dec 11 26 and Best if USED BY Dec 18 26 — 769 cases (13 bags/case)
Firm / distribution: Saratoga Potato Chips LLC — The recalled J. HIGGS Loaded Bacon and Cheddar Potato Chips were distributed in the states of Florida, Indiana, Kentucky, Ohio, Tennessee, and Maryland and sold in Save A Lot stores.
- Why it was recalled
- May contain undeclared aspartame.
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: Best if use by: 032327 TA — 2100 units
Firm / distribution: Refresco Beverages US Inc — Florida with further downstream distribution to retail stores
- Why it was recalled
- defective packaging; packaging can rupture/explode during cooking.
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: Best By Date: 2027 09 14 Lot # 2576 — 4544 cases / 27,324 individual retail units
Firm / distribution: DARING FOODS INC — Product was distributed to a single retail grocery chain customer with multiple locations in Florida and one location in North Carolina. A total of 6 locations received recalled product.
- Why it was recalled
- Lack of process control
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: Lot# SER-081726-1-10, Beyond Use Date: 10/01/2026. — 7 vials
Firm / distribution: Houston Rx LLC — Nationwide in the USA.
- Why it was recalled
- Presence of Foreign Tablets/Capsules
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: Lot, expiry: [100 Tablets] Lots 8634085, 8635085, 8636085, exp 07/2027; [500 Tablets] Lot 8633085, exp 07/2027 — 240,448 cartons
Firm / distribution: Teva Pharmaceuticals USA, Inc — US Nationwide.
Full product description
Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-620-01; NDC Unit Dose: 60687-620-11
- Why it was recalled
- Presence of Foreign Tablets/Capsules
- What to do
- The recall is ongoing. Follow the firm and FDA instructions.
Affected identifiers: Lot 1028135, 1029555; Exp. Date 07/31/2027 — 5,363 cartons
Firm / distribution: American Health Packaging — US Nationwide