Safety Recalls

15,259 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 5,351–5,400 of 15,259

• Food Recall · July 25, 2025

  Tropicale Foods, LLC

  La Michoacana Mango Con Crema Single Serve Paleta 3.75oz UPC: 7-67778-00008-2

  Product label includes the ingredient CREAM but does not include Milk as the source.

  Class II

• Food Recall · July 25, 2025

  Distinctive Foods LLC

  Frederik's by Meijer Artisan Baked Sea Salt flatbread crackers net wt 5.5oz. UPC 7 13733 00048 2

  Undeclared sesame.

  Class II

• Medical Device Recall · July 25, 2025

  Olympus Corporation of the Americas

  Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410 Surgical Energy Platform (SEP). Model Number: WA91327U. The ESG-410 Electrosurgical Generator is an elect

  Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.

  Class II

• Food Recall · July 25, 2025

  Tropicale Foods, LLC

  Helados Mexico Choco-Dipped Minis Variety Paletas 12-Count 18oz UPC: 6-82082-81215-5 UPC: 6-82082-41215-7

  Product label includes the ingredient CREAM but does not include Milk as the source.

  Class II

• Food Recall · July 25, 2025

  Gelsons

  Gelson's Hummus; Low Sodium No Cholesterol Classic NET WT 10OZ (283g) UPC: 23631-10260

  Gelson branded Hummus product labels do not include storage instructions "keep refrigerated"

  Class II

• Medical Device Recall · July 25, 2025

  Merit Medical Systems, Inc.

  10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / 00884450821305 MAPTEN42 / 00884450832509 MAPTEN452 / 00884450821329 The 10Fore Hemostasis Valve is intended to maintain hemostasi

  Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.

  Class II

• Medical Device Recall · July 24, 2025

  Dexcom, Inc.

  Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: versions 2.8.0 and earlier Product Description: D

  The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0 or earlier) and Dexcom ONE+ CGM System using iOS and Android App software (versions 1.4.0 or earlier), henceforth referred to as the App. The affected App does not provide an expected "Sensor Failed" alert when the transmitter sends a "transmitterFailed" error message to the App when the CGM experiences a hardware or firmware failure. Instead, the App ends the CGM sensor session, stops reporting glucose values and displays the Start Sensor screen or No active sensor message without alerting the user, which can lead to missed detection of a hyperglycemic or hypoglycemic event and a delay in treatment.

  Class I

• Food Recall · July 24, 2025

  The Bonami Baking Company, Inc.

  Wheat Hamburger Buns --- Ingredient Declaration: Water, Whole Wheat Flour, Enriched Wheat Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamin Mononitrate (Vitamin B1) Riboflavin

  Undeclared milk and/or eggs from sub-ingredients and/or Contains statement.

  Class II

• Medical Device Recall · July 24, 2025

  THOR Photomedicine Ltd

  Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visib

  The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.

  Class II

• Medical Device Recall · July 24, 2025

  Dexcom, Inc.

  Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM Android App Model/Catalog Number: SW12299 Software Version: version 2.8.0 and earlier Product Description: De

  The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0 or earlier) and Dexcom ONE+ CGM System using iOS and Android App software (versions 1.4.0 or earlier), henceforth referred to as the App. The affected App does not provide an expected "Sensor Failed" alert when the transmitter sends a "transmitterFailed" error message to the App when the CGM experiences a hardware or firmware failure. Instead, the App ends the CGM sensor session, stops reporting glucose values and displays the Start Sensor screen or No active sensor message without alerting the user, which can lead to missed detection of a hyperglycemic or hypoglycemic event and a delay in treatment.

  Class I

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, upbeat

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Food Recall · July 24, 2025

  The Bonami Baking Company, Inc.

  Whole Grain Par Baked Jalapeno Cheddar Bagel --- Ingredient Declaration: Whole White Wheat Flour, Enriched Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamine Mononitrate (Vitam

  Undeclared milk from Contains statement.

  Class II

• Consumer Product Recall · July 24, 2025

  Shenzhen Yiqun Technology Co. Ltd. dba Aiho Inc., of China

  Aiho Dressers

  The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers fail to meet the mandatory standard, as required by the STURDY Act.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Jinanmingzhongdashangmaoxiaoshouyouxiangongsi, dba Minongad, of China

  LED Gloves

  The recalled LED gloves violate the mandatory standard for toys containing coin batteries because the compartment that holds the batteries can be easily accessed and opened by children. Additionally, the spare coin batteries provided with the toys are not in child-resistant packaging and do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, spicy lemonade

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Medical Device Recall · July 24, 2025

  Dentsply IH, Inc.

  Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04S / 6802034 Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-

  The defect in the thread area will not allow the device to fully engage with an implant or analog (implant replica used for prosthetic modeling). The threads will only engage approximately 2 rotations as opposed to full engagement which is approximately 5 rotations. This equates to approximately 1mm difference in depth of engagement.

  Class II

• Medical Device Recall · July 24, 2025

  Dexcom, Inc.

  Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number: SW12300 Software Version: version 2.8.0 and earlier Product Description: Dexcom

  The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0 or earlier) and Dexcom ONE+ CGM System using iOS and Android App software (versions 1.4.0 or earlier), henceforth referred to as the App. The affected App does not provide an expected "Sensor Failed" alert when the transmitter sends a "transmitterFailed" error message to the App when the CGM experiences a hardware or firmware failure. Instead, the App ends the CGM sensor session, stops reporting glucose values and displays the Start Sensor screen or No active sensor message without alerting the user, which can lead to missed detection of a hyperglycemic or hypoglycemic event and a delay in treatment.

  Class I

• Drug Recall · July 24, 2025

  Cipla USA, Inc.

  Albuterol Sulfate, Inhalation Aerosol, 90 mcg, 200 metered Inhalations, NET CONTENT 6.7 g, Manufactured by: Cipla Ltd, Indore, SEZ, Pithampur, India; Manufactured for: Cipla USA, Inc. 10 Independence

  Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.

  Class III

• Medical Device Recall · July 24, 2025

  Beckman Coulter, Inc.

  MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of ae

  Due to the likely presence of contamination in well(s).

  Class II

• Medical Device Recall · July 24, 2025

  Dexcom, Inc.

  Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ Android CGM App Model/Catalog Number: SW14245 Software Version: versions 1.4.0 and earlier Product Descriptio

  The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0 or earlier) and Dexcom ONE+ CGM System using iOS and Android App software (versions 1.4.0 or earlier), henceforth referred to as the App. The affected App does not provide an expected "Sensor Failed" alert when the transmitter sends a "transmitterFailed" error message to the App when the CGM experiences a hardware or firmware failure. Instead, the App ends the CGM sensor session, stops reporting glucose values and displays the Start Sensor screen or No active sensor message without alerting the user, which can lead to missed detection of a hyperglycemic or hypoglycemic event and a delay in treatment.

  Class I

• Medical Device Recall · July 24, 2025

  Boston Scientific Corporation

  ENDOTAK RELIANCE G/SG, transvenous defibrillation lead, implantable cardioverter defibrillator (non-CRT); Model Nos. 0160, 0161, 0162, 0163, 0164, 0165, 0166, 0167, 0170, 0171, o182, 0173, 0174, 0175,

  Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.

  Class I

• Medical Device Recall · July 24, 2025

  Boston Scientific Corporation

  ENDOTAK RELIANCE G/SG with 4-SITE Connector, transvenous defibrillation lead, Permanent Defibrillator Electrodes; Model Nos. 0282, 0283, 0285, 0286, 0292, 0293, 0295, 0296

  Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.

  Class I

• Food Recall · July 24, 2025

  Superior Foods Company

  Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. in plastic tub UPC 4061462440151

  foreign material (plastic)

  Class II

• Medical Device Recall · July 24, 2025

  Boston Scientific Corporation

  RELIANCE 4-FRONT, endocardial cardioversion/defibrillation and pace/sense lead, Permanent Defibrillator Electrodes; Model Nos. 0654, 0655, 0657, 0658, 0682, 0683, 0685, 0686, 0692, 0693, 0695, 0696

  Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.

  Class I

• Food Recall · July 24, 2025

  The Bonami Baking Company, Inc.

  Chocolate Croissants --- Ingredients: HARVEST KING FLOUR, Butter, Water, Sugar, Yeast, Salt, Chocolate Chips (Sugar, Chocolate, Butter

  Undeclared wheat, milk, and soy (from soy lecithin) from sub-ingredients.

  Class II

• Consumer Product Recall · July 24, 2025

  ShangYu North Electron Manufacture Co. Ltd., of China

  Frigidaire-brand Minifridges, models EFMIS129, EFMIS137, EFMIS149 and EFMIS175, limited to the listed serial numbers

  The minifridges' internal electrical components can short circuit and ignite the surrounding plastic housing, posing fire and burn hazards.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Lichang E-Commerce, Inc, of Hacienda Heights, California

  LIVACTI Retractable Safety Gates

  The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment.

  Unclassified

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, sweet greens

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Medical Device Recall · July 24, 2025

  THOR Photomedicine Ltd

  Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spe

  The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.

  Class II

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, cashew milk

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Consumer Product Recall · July 24, 2025

  Diamond G Forest Products LLC, of Patterson, Georgia

  Georgia Pine Gum Spirits of Turpentine Bottles

  The bottles contain turpentine, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are ingested by young children.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Transpro US Inc., of Paterson, New Jersey

  Transpro Electric Scooters

  The battery compartment of the recalled light-up ruler bracelets can be opened easily by children allowing access to the button cell batteries, violating the battery-operated toys requirements under the mandatory standard for toys. If a child swallows a button cell or coin battery, it can cause serious injuries, internal chemical burns or death.

  Unclassified

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, DETOX GREENS

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, cashew coffee milk

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Food Recall · July 24, 2025

  The Bonami Baking Company, Inc.

  Cheddar Bagel --- Ingredient Declaration: Harvest King Flour, All purpose flour, kosher salt, light brown sugar, yeast, water, malt, cheddar cheese --- The Bonami Baking Company

  Undeclared wheat and milk from sub-ingredients.

  Class II

• Medical Device Recall · July 24, 2025

  THOR Photomedicine Ltd

  Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visib

  The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.

  Class II

• Food Recall · July 24, 2025

  Everpress Juice

  JUICE from the Raw, pineapple mint

  Under-processed product may contain pathogenic bacteria that could harm to humans.

  Class I

• Food Recall · July 24, 2025

  The Bonami Baking Company, Inc.

  Whole Wheat Chocolate Croissants --- Ingredients: Whole White Wheat Flour, Enriched Wheat Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamine Mononitrate (Vitamin B1), Riboflavi

  Undeclared milk and soy (from soy lecithin) from sub-ingredients.

  Class II

• Medical Device Recall · July 24, 2025

  Dentsply IH, Inc.

  Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software Version: n/a Product Description: The Atlantis intraoral feature locating object fo

  The defect in the thread area will not allow the device to fully engage with an implant or analog (implant replica used for prosthetic modeling). The threads will only engage approximately 2 rotations as opposed to full engagement which is approximately 5 rotations. This equates to approximately 1mm difference in depth of engagement.

  Class II

• Medical Device Recall · July 24, 2025

  THOR Photomedicine Ltd

  Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectr

  The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.

  Class II

• Medical Device Recall · July 24, 2025

  Dexcom, Inc.

  Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.4.0 and earlier Product Description: D

  The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0 or earlier) and Dexcom ONE+ CGM System using iOS and Android App software (versions 1.4.0 or earlier), henceforth referred to as the App. The affected App does not provide an expected "Sensor Failed" alert when the transmitter sends a "transmitterFailed" error message to the App when the CGM experiences a hardware or firmware failure. Instead, the App ends the CGM sensor session, stops reporting glucose values and displays the Start Sensor screen or No active sensor message without alerting the user, which can lead to missed detection of a hyperglycemic or hypoglycemic event and a delay in treatment.

  Class I

• Consumer Product Recall · July 24, 2025

  Shenzhen Fengqisi Car Industry Co., Ltd., dba FENGQS, of China

  FENGQS F7 Pro E-bikes

  The e-bikes' lithium-ion battery can overheat and ignite, posing serious fire and burn hazards to consumers.

  Unclassified

• Consumer Product Recall · July 24, 2025

  iMirror Inc., of Rancho Cucamonga, California

  Rechargeable Electric Bug Zapper Racket, Fly Swatter, and Mosquito Swatter for Indoor and Outdoor use

  The rechargeable battery in the Electric Bug Zapper Racket, Fly Swatter, and Mosquito Swatter can catch fire when used for extended periods of time.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Apollo Imports Inc., of Newark, Delaware

  Apollo City Model Year 2024 Electric Scooters

  The weld line on the electric scooter can crack, causing the stem to break and posing fall and injury hazards.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Creekwood Naturals, of Corona, California

  100% Natural Pure Gum Spirits of Turpentine Bottles

  The recalled bottles contain turpentine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The turpentine bottles violate the mandatory standard for child-resistant packaging, posing a deadly poisoning hazard to young children.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Innovative Designs LLC, of New York

  Minecraft Light-Up Slap Ruler Bracelets

  The battery compartment of the recalled light-up ruler bracelets can be opened easily by children, allowing access to the button cell batteries, violating the battery-operated toys requirements under the mandatory standard for toys. If a child swallows a button cell or coin battery, it can cause serious injuries, internal chemical burns or death.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Pura Scents Inc., of Pleasant Grove, Utah

  Pura 4 Smart Home Fragrance Diffusers with detachable covers

  The magnets on the inside cover can detach, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.

  Unclassified

• Consumer Product Recall · July 24, 2025

  Winston Products, of Glenwillow, Ohio

  HydroTech 5/8-inch Expandable Burst-Proof Hoses

  The recalled hoses can burst, posing an impact hazard and a risk of temporarily impaired hearing.

  Unclassified

• Food Recall · July 23, 2025

  Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods

  Sukhi's, CLASSIC CURRY INDIAN CURRY SAUCE, NET WT 3 OZ., UPC 7-67226-00165-4, DISTRIBUTED BY: SUKHI'S GOURMET INDIAN FOODS 25823 CLAWITER ROAD, HAYWARD, CA 94545 USA

  Potential contamination with foreign objects (metal pieces).

  Class II

• Medical Device Recall · July 23, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DYNJG901001B CRANIOTOMY DYNJ908819B KIT CRANIOTOMY (only units from

  Kits contain SureStep Foley Tray Systems recalled by BD that include incorrect product information insert sheets. If a mislabeled tray is used, patient risk ranges from minor injury to injury that requires medical intervention, such as infection or local/systemic allergic reaction (anaphylaxis).

  Class II