Safety Recalls
RSS ↗15,768 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 51–100 of 15,768
- Unclassified
Consumer Product Recall · August 13, 2026
Guangzhou Yide Toys Co., Ltd., of China
TooyBing Wooden Bead Stacking ToysThe recalled toys violate the small parts ban because they are intended for children under three years old and the wooden beads pose a deadly choking hazard to young children.
- Unclassified
Consumer Product Recall · August 13, 2026
Yongkang Dingchang Industry and Trade Co., Ltd, of China
Youth All-Terrain Vehicles (ATVs), model XW-A19The recalled youth ATVs violate the mandatory safety standard for ATVs because the parking brakes fail to hold and the ATV's speed limiting device is not set to the restricted speed required for children ages six (6) and older, posing a crash hazard. Additionally, the ATVs are missing the required rear safety reflectors, reducing visibility of the youth ATV to other vehicles, posing a deadly crash hazard.
- Unclassified
Vehicle Recall · August 7, 2026
2024 HUSQVARNA FE 350SCracks or breaks in the rear brake caliper can reduce braking ability, increasing the risk of a crash.
- Unclassified
Vehicle Recall · August 7, 2026
2026 PETERBILT 579An incorrectly installed quick release valve that does not function properly can increase the risk of a crash.
- Unclassified
Vehicle Recall · August 7, 2026
Toyota Motor Engineering & Manufacturing
2026 TOYOTA GRAND HIGHLANDERA broken rear axle carrier can cause a sudden loss of vehicle stability and control, increasing the risk of a crash.
- Unclassified
Vehicle Recall · August 7, 2026
2023 BMW X4, 2023 TOYOTA SUPRA, 2024 BMW X3, 2024 BMW X4, 2024 TOYOTA SUPRA, 2025 BMW X4Fire increases the risk of injury.
- Unclassified
Consumer Product Recall · August 6, 2026
Fitueyes, Inc., of City of Industry, California
Laziza DressersThe 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 death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · August 6, 2026
Generac Power Systems Inc., of Waukesha, Wisconsin
DR Power PRO MAX30 30" Walk-Behind Power Lawn MowersThe recalled mowers violate the mandatory safety standard for walk-behind power lawn mowers because the blades can operate without the blade control system engaged or continue to operate even after the release of the control, posing a serious laceration hazard.
- Unclassified
Consumer Product Recall · August 6, 2026
HEAD USA, Inc. dba Head Watersports of Delray Beach, Florida
Apeks Second Stage Scuba RegulatorsThe recalled second stage regulators can restrict air flow to the user at depths exceeding 45 meters (approximately 147 feet), posing risk of serious injury or death from a drowning hazard.
- Unclassified
Consumer Product Recall · August 6, 2026
BUSOHA Magnetic Fidget Slider ToysThe magnetic fidget sliders violate the mandatory standard for toys because they can liberate loose magnets 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, blood poisoning and death.
- Unclassified
Consumer Product Recall · August 6, 2026
Shenzhen Okabesini Technology Co., Ltd., dba Okabesini-us, of China
Little Rawr Silicone Pull String Teething ToysThe recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's throat and become lodged, posing a serious risk of respiratory distress and a deadly choking hazard.
- Unclassified
Consumer Product Recall · August 6, 2026
Vanderhall North America, LLC, of Provo, Utah
Vanderhall Brawley GTS electric recreational off highway vehiclesThe recalled recreational off highway vehicle can maintain speed or accelerate when the accelerator pedal is released, posing a risk of serious injury or death from a crash hazard.
- Unclassified
Consumer Product Recall · August 6, 2026
Voomf Play Yard and Crib MattressesThe recalled mattresses violate the mandatory safety standard for crib mattresses because the mattresses may not adequately fit certain play yards, posing a deadly entrapment hazard. Babies can suffocate in gaps between an undersized mattress, or extra padding, and side walls of a product, especially when the infant's face becomes trapped against the side and the mattress, preventing the infant from breathing. Furthermore, the full-sized crib mattresses violate the mandatory flammability standard for mattress sets, posing a risk of serious injury or death from fire.
- Unclassified
Consumer Product Recall · August 6, 2026
Courant Spliced Kalimba Climbing RopesThe spliced termination ends on the recalled ropes can fail unexpectedly, posing a risk of serious injury or death from fall hazard.
- Unclassified
Consumer Product Recall · August 6, 2026
Changsha 678 Trading Co., Ltd., dba Luqiba, of China
Liuqibax Adult Bed RailsThe 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 rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
- Unclassified
Consumer Product Recall · August 6, 2026
KC IMPORTS AND EXPORTS, Inc., of Vernon, California
Laser & LED Light Mini Laser Pointer KeychainsThe Mini Laser Pointer Keychains violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product 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
Consumer Product Recall · August 6, 2026
Huoshan County Haozhou E-commerce Co, doing business as PIXLABBY, of China
PIXLABBY Silicone Sensory Magnetic Fidget SlidersThe magnetic fidget sliders violate the mandatory standard for toys because they can liberate loose high-powered magnets 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, blood poisoning and death.
- Unclassified
Consumer Product Recall · August 6, 2026
OKK Trading, Inc., of Vernon, California
Easter LED HeadbandsThe recalled headbands violate the mandatory safety standard for toys with button cell and coin batteries because the lithium coin batteries can be accessed easily by children, posing an ingestion hazard. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Unclassified
Consumer Product Recall · August 6, 2026
Winston Porter and Seeday 3-Drawer, 4-Drawer and 5-Drawer DressersThe 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 death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · August 6, 2026
Changsha Yuelu District Ruiwu E-Commerce Co., Ltd., dba WURUI.BABY, of China
Wnttmt Baby WalkersThe 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 step, posing a deadly fall hazard. In addition, the infant walkers have leg openings that allow the child to slip down until the child's head can become entrapped, posing a risk of serious injury or death.
- Unclassified
Consumer Product Recall · August 6, 2026
Louisville Ladder, Inc., of Louisville, Kentucky
Louisville, Featherlite, Lite & Century Attic Stairway Ladders with gas strutsThe bolts on the attic stairway ladders can break while in use, posing a risk of serious injury or death from fall hazard.
- Unclassified
Consumer Product Recall · August 6, 2026
Senyu Era International Co. Limited, dba Syera, of China
Space Astronaut LED Finger LightsThe recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- Unclassified
Consumer Product Recall · August 6, 2026
EEMB USA, doing business as A2batt, Inc., of Redlands, California
EEMB Lithium-ion Coin Battery Chargers with Rechargeable 2032 BatteriesThe recalled battery chargers violate the mandatory standard for consumer products containing button cell or coin batteries, because the charger has lithium coin batteries that can be accessed easily by children. In addition, the coin batteries provided with the battery charger are not in child-resistant packaging, and the packaging does not have the warnings, as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Class II
Drug Recall · August 5, 2026
Zydus Pharmaceuticals (USA) Inc
Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Matoda, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington,CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.
- Class II
Drug Recall · August 4, 2026
Novartis Pharmaceuticals Corporation
Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 007Failed Dissolution Specifications
- Class II
Drug Recall · August 3, 2026
SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, MahCGMP Deviations:Noted during FDA inspection
- Class II
Drug Recall · August 3, 2026
TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, GuCGMP Deviations:Noted during FDA inspection
- Class II
Drug Recall · August 3, 2026
SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, MahCGMP Deviations:Noted during FDA inspection
- Class II
Drug Recall · August 3, 2026
TADALAFIL USP, 0.100 KG, 0.1KG(100gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania,CGMP Deviations:Noted during FDA inspection
- Class II
Drug Recall · August 3, 2026
TADALAFIL USP, 0.500 KG, 0.500KG(500gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, MahesaniaCGMP Deviations:Noted during FDA inspection
- Class I
Drug Recall · July 31, 2026
Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufactured by: Liebel-Flarsheim Company LLC, RaleiPresence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
- Unclassified
Consumer Product Recall · July 30, 2026
Changzhou Jiaxuan Intelligence Furniture Co., Ltd., of China
EnHomee 15-Drawer 51" DressersThe 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 death to children. The dressers violate the mandatory safety standards as required by the STURDY Act.
- Unclassified
Consumer Product Recall · July 30, 2026
Golden Link, of Middletown, New York
Fantastic Four Drinking Cups and Captain America Popcorn Helmet Containers with LED LightsThe cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. In addition, the products do not bear the warning labels required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- Unclassified
Consumer Product Recall · July 30, 2026
Hangzhouyuefangjiajuyongpinyouxiangongsi, dba OCTROT, of China
OCTROT Electric Thows and BlanketsThe 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.
- Unclassified
Consumer Product Recall · July 30, 2026
TT Trsmima Zipline Kits and Zipline Spring BrakesThe 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 safely slow a rider down and the kit design does not include an emergency brake, posing collision and fall hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
Galanz Retro RefrigeratorsThe recalled refrigerators' internal electrical components can short circuit and ignite, posing a risk of serious injury or death from fire and burn hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
Shantou Chenghai District Zhiwan Classroom Trading Co., doing business as TOYHW, of China
Mommy's Baby Lovely Deluxe Baby Doll PlaysetsThe 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, posing a deadly choking hazard.
- Unclassified
Consumer Product Recall · July 30, 2026
Guangzhou Dida Electronic Commerce Co., Ltd. dba CetoPMax, of China
Cpzzkq Baby LoungersThe recalled baby loungers violate the mandatory safety standard for infant support cushions because the padding can obstruct an infant's breathing, posing a serious risk of injury or deadly suffocation hazard.
- Unclassified
Consumer Product Recall · July 30, 2026
Jake's Fireworks, Inc., of Pittsburg, Kansas
World Class Fireworks "Skull Strobe" RocketsThe recalled fireworks rockets can explode prematurely before reaching their intended height, posing explosion and burn hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
Hangzhou Xinyanchuangxin Tech. Co., Ltd. dba Mangohood Direct, of China
Mangohood Direct Kids Kitchen Standing Towers, Model LT003The 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 serious injury and death due to tip over, fall and entrapment hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
Joyin US Corp., of Chandler, Arizona
Sloosh Dive Sticks, models 40041, 40003 and 16154The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children may fall or land on a dive stick, resulting in serious piercing injuries. Facial and eye injuries are also possible when children attempt to retrieve the sticks underwater.
- Unclassified
Consumer Product Recall · July 30, 2026
Shenzhen Street Cat Technology Co., Ltd., dba OCOOPA Direct, of China
OCOOPA Rechargeable Hand WarmersThe 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.
- Class II
Drug Recall · July 30, 2026
CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-603-51Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
- Unclassified
Consumer Product Recall · July 30, 2026
Shenzhen Muqiqu Creative Development Co. Ltd., of China
Woodure Toddler Kitchen Step StoolsThe 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 serious injury and death due to tip over, fall and entrapment hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
HARPPA, Inc., of Denver, Colorado
Nordi Foldable Toddler Tower StoolsThe 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 serious injury and death due to tip over, fall and entrapment hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
BenQ America Corp., of Costa Mesa, California
BenQ GV31 Portable ProjectorsThe recalled projectors' lithium-ion battery can overheat, posing a risk of serious injury or death from fire and burn hazards.
- Unclassified
Consumer Product Recall · July 30, 2026
Luoyang Siqi Trading Co., Ltd., dba KAIFAM, of China
KAIFAM 5-Drawer DressersThe 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 death to children. The dressers violate the mandatory safety standards as required by the STURDY Act.
- Class II
Drug Recall · July 29, 2026
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-0Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
- Class II
Drug Recall · July 29, 2026
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
- Class II
Drug Recall · July 29, 2026
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material