Recalls in July 2026 (page 4)
416 recalls.
- FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: recall (Biofire Defense)
Medical deviceClass IIReported August 12, 2026 · Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the... recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported August 12, 2026 · Devices could potentially contain an occluded or partially occluded Guedel Airway tip. - FORWARD Oral Airway Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported August 12, 2026 · Devices could potentially contain an occluded or partially occluded Guedel Airway tip. - Mellish Island Super Skin recall (Mellish Island Corp)
FoodClass IIReported August 5, 2026 · Firm's finished product label does not declare the source of marine collagen which was determined to be fish. - Dabigatran Etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported August 5, 2026 · Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for... - Dabigatran Etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported August 5, 2026 · Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for... - Dabigatran Etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported August 5, 2026 · Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for... - Mycophenolate Mofetil for Injection USP recall (MYLAN PHARMACEUTICALS INC)
DrugClass IIReported August 5, 2026 · Presence of precipitate - Azelaic Acid Gel recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported August 5, 2026 · CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received. - Dorzolamide HCl and Timolol Maleate Ophthalmic Solution recall (MICRO LABS USA INC)
DrugClass IIReported August 5, 2026 · Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops. - Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - OsteoBallast recall (IsoTis OrthoBiologics, Inc.)
Medical deviceClass IIReported August 5, 2026 · Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were... - OCOOPA Direct Recalls 1.5 Million Rechargeable Hand Warmers Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported; Imported by Shenzhen Street Cat Technology
Consumer productReported July 31, 2026 · The lithium-ion battery in the recalled hand warmers can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards. - Woodure Toddler Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Shenzhen Muqiqu Creative Development
Consumer productReported July 31, 2026 · The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of... - Recall of Cpzzkq Baby Loungers Expanded Due to Risk Serious Injury or Death from Suffocation Hazard; Violate Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax
Consumer productReported July 31, 2026 · The recalled baby loungers violate the mandatory safety standard for infant support cushions because the padding can obstruct an infant's breathing, posing a... - Mommy's Baby Lovely Deluxe Baby Doll Playsets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Temu by TOYHW
Consumer productReported July 31, 2026 · The recalled doll playsets violate the small parts ban because the toys are for children under three years old and some of the accessories are small parts... - Mangohood Direct Kids Kitchen Standing Towers Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Hangzhou Xinyanchuangxin
Consumer productReported July 31, 2026 · The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of... - Joyin Expands Recall of Sloosh Dive Sticks Due to Risk of Serious Injury from Impalement; Violate Federal Dive Sticks Ban
Consumer productReported July 31, 2026 · The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children... - Jake's Fireworks Recalls World Class Fireworks "Skull Strobe" Rockets Due to Risk of Serious Injury from Explosion and Burn Hazards
Consumer productReported July 31, 2026 · The recalled fireworks rockets can explode prematurely before reaching their intended height, posing explosion and burn hazards. - Heated Sherpa Throws and Blankets Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Sold on Amazon by OCTROT
Consumer productReported July 31, 2026 · The electrical cord on the recalled throws and blankets can detach and ignite, posing a risk of serious injury or death from fire, burn and shock hazards. - HARPPA Recalls Nordi Toddler Tower Stools Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards
Consumer productReported July 31, 2026 · The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of... - Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported July 31, 2026 · The cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries... - Galanz Americas Recalls Retro Refrigerators Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
Consumer productReported July 31, 2026 · The recalled refrigerators' internal electrical components can short circuit and ignite, posing a risk of serious injury or death from fire and burn hazards. - BenQ America Recalls GV31 Portable Projectors Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported July 31, 2026 · The recalled projectors' lithium-ion battery can overheat, posing a risk of serious injury or death from fire and burn hazards. - 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by KAIFAM
Consumer productReported July 31, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - 15-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Enhomee-Direct
Consumer productReported July 31, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Trsmima Zipline Kits and Zipline Spring Brakes Recalled Due to Fall and Collision Hazards; Manufactured by Trsmima
Consumer productReported July 31, 2026 · The zipline kit's steel cable, turnbuckle and seat can detach or break during use, posing a fall hazard. The zipline spring brakes are not stiff enough to... - Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units recall (Man Fon, Inc.)
FoodClass IIReported July 29, 2026 · No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6. - Man Fon Inc. Won Ton Wrappers Extra Thin recall (Man Fon, Inc.)
FoodClass IIReported July 29, 2026 · Undeclared colors: Yellow#5, and Yellow#6. - Organic Moringa Powder recall (Green Jeeva LLC)
FoodClass IReported July 29, 2026 · Moringa Powder ingredient positive for salmonella - Brooklyn Roasting Company Pasteurized Cold Brew Concentrate recall (Brooklyn Roasting Works LLC)
FoodClass IIReported July 29, 2026 · Ambient storage of the product may lead to Clostridium botulinum toxin formation. - Trokendi XR recall (Supernus Pharmaceuticals, Inc.)
DrugClass IIIReported July 29, 2026 · Failed Dissolution Specifications - Glycopyrrolate Oral Solution recall (Precision Dose Inc.)
DrugClass IIReported July 29, 2026 · Failed Impurities/Degradation Specifications - Xylocaine recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Xylocaine recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Naropin recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Lidocaine HCl Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Glycopyrrolate Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in product - Rising recall (Rising Pharma Holding, Inc.)
DrugClass IIReported July 29, 2026 · Presence of Precipitate: medication was crystallizing and particles floating in the bottle - Rohto Cooling Eye Drops Cool Relief recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Dry Aid recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Dry Aid recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Digi Eye recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Optic Glow recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Max Strength recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Max Strength recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops ALL-IN-ONE recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Lidolog Kit recall (Asclemed USA Inc.)
DrugClass IIIReported July 29, 2026 · Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan - Amlodipine and Olmesartan Medoxomil Tablets recall (Ascend Laboratories, LLC)
DrugClass IIReported July 29, 2026 · Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities. - Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported July 24, 2026 · The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children. - CuddleCubs Creations Teething Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by YouRfocus
Consumer productReported July 24, 2026 · The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and... - OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold Exclusively on Amazon by Yuanxinxiang
Consumer productReported July 24, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act
Consumer productReported July 24, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Aojieni Silicone Recalls Sili Factory Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
Consumer productReported July 24, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - 12-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Romorgniz
Consumer productReported July 24, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - EnHomee 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by Raybee-Direct
Consumer productReported July 24, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or... - Organic Whole Blueberries recall (Frutas y Hortalizas del Sur S.A.)
FoodClass IReported July 22, 2026 · Potential E. coli O145:H28 Contamination - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 22, 2026 · Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator - CLEVIPREX recall (Chiesi USA, Inc.)
DrugClass IIReported July 22, 2026 · Lack of Assurance of Sterility - MNIENT Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported July 17, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported July 17, 2026 · The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard. - SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
Consumer productReported July 17, 2026 · The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of... - Noerishia Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Hurzein
Consumer productReported July 17, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
Consumer productReported July 17, 2026 · The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of... - Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
Consumer productReported July 17, 2026 · The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death. - Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
Consumer productReported July 17, 2026 · The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning. - Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning
Consumer productReported July 17, 2026 · The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or... - Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
Consumer productReported July 17, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard
Consumer productReported July 17, 2026 · The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard. - TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards
Consumer productReported July 17, 2026 · The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards. - Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo Technology
Consumer productReported July 17, 2026 · The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act.... - Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
Consumer productReported July 17, 2026 · The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard. - Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
Consumer productReported July 17, 2026 · The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children.... - Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Consumer productReported July 10, 2026 · Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit... - Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported July 10, 2026 · The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards. - WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Walmart.com by Wonder Stone Toys
Consumer productReported July 10, 2026 · The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a...