Recalls in Florida (page 41)
4115 recalls.
- Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - BD Pyxis MedStation ES recall (CareFusion 303, Inc.)
Medical deviceClass IIReported December 31, 2025 · Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a... - Draeger Vapor 3000. Unheated recall (Draeger, Inc.)
Medical deviceClass IReported December 31, 2025 · A certain component of affected devices was not delivered within specification and contained impurities. - Draeger Vapor 2000. Unheated recall (Draeger, Inc.)
Medical deviceClass IReported December 31, 2025 · A certain component of affected devices was not delivered within specification and contained impurities. - Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. recall (Silvestri Sweets Inc dba Carousel Candies)
FoodClass IReported December 31, 2025 · Undeclared pecan - Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag. 5 oz. recall (Silvestri Sweets Inc dba Carousel Candies)
FoodClass IReported December 31, 2025 · Undeclared wheat - Noxafil Powdermix recall (Merck Sharp & Dohme LLC)
DrugClass IIReported December 31, 2025 · Presence of particulate matter: potential presence of metal particulates in the product. - Merck Emend recall (Merck Sharp & Dohme LLC)
DrugClass IIReported December 31, 2025 · Presence of particulate matter: potential presence of metal particulates in the product. - Restore Clinician Programmer Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported December 31, 2025 · Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and... - LYFO DISK recall (Microbiologics Inc)
Medical deviceClass IIReported December 31, 2025 · Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. - KWIK-STIK 6-Pack recall (Microbiologics Inc)
Medical deviceClass IIReported December 31, 2025 · Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. - KWIK-STIK 2-Pack recall (Microbiologics Inc)
Medical deviceClass IIReported December 31, 2025 · Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the... - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users... - Brand Name: Alcon Laboratories recall (Alcon Research LLC)
Medical deviceClass IReported December 31, 2025 · Ophthalmic procedure packs may have incomplete seals affecting sterility. - Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common... recall (AGFA Healthcare Corp.)
Medical deviceClass IIReported December 31, 2025 · It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on... - Celebration Herbals Senna Leaf Herbal Tea 24 Teabags recall (CELEBRATION HERBALS US)
FoodClass IIReported December 24, 2025 · possible salmonella - BIOSURE HA SCREW recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported December 24, 2025 · Removal of affected lot of screws due to labeling error. - Intelerad InteleShare software recall (DICOM Grid, Inc.)
Medical deviceClass IIReported December 24, 2025 · Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing... - HemosIL SynthAFax. Partial Thromboplastin Time Tests. recall (Instrumentation Laboratory)
Medical deviceClass IIIReported December 24, 2025 · Recalled lots were manufactured with double the amount of preservative concentration. - Orthofix NorthStar OCT Navigation Surgical Technique Guide recall (SEASPINE ORTHOPEDICS CORPORATION)
Medical deviceClass IIReported December 24, 2025 · The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as... - Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IReported December 24, 2025 · Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death. - Ciclopirox Shampoo recall (SUN PHARMA /TARO)
DrugClass IIReported December 24, 2025 · Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Baclofen Tablets USP recall (Golden State Medical Supply Inc.)
DrugClass IIReported December 24, 2025 · Presence of Foreign Tablets/Capsules - Hardware configuration of the BeneVision Central Monitoring System recall (Mindray DS USA, Inc. dba Mindray North America)
Medical deviceClass IIReported December 24, 2025 · When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing. - GE Healthcare Carestation anesthesia system Power Management Board recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - GE Healthcare Carestation anesthesia system recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - GE Healthcare Carestation anesthesia system recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - Meaicezli Play Purse Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Angeer-US
Consumer productReported December 24, 2025 · The children's toy violates the mandatory standard for toys because the toy cell phone contains button cell batteries and the toy tablet contains a lithium... - Blue Wave Recalls Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard
Consumer productReported December 18, 2025 · The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk. - SereneLife Home Recalls Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard
Consumer productReported December 18, 2025 · This recall involves all SereneLife brand above-ground pools 48 inches and taller. Models SLPORND15 and SLPORND18 are included in this recall. Model... - ANNQUAN Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold on Amazon by Hefei Juyuan Sporting Development
Consumer productReported December 18, 2025 · The power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can... - JOKOSIS Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by JOKOSIS
Consumer productReported December 18, 2025 · 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... - KKL Fabric 9-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 HK Brilliant
Consumer productReported December 18, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing a serious tip-over and entrapment hazards that can result in injuries or death... - Feel The Beard Recalls Minoxidil Beard Growth Serum Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported December 18, 2025 · The beard serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging... - Plantimex Recalls Mamisan Lidocaine Ointment Containers Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported December 18, 2025 · The ointment contains lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The ointment's packaging is... - 17 Stories Furniture 18-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by Shenzhen Jinhongzhen Technology Co
Consumer productReported December 18, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazard that can result in injuries or death to... - Currey & Company Recalls Electra Chandeliers Due to Impact Injury Hazard
Consumer productReported December 18, 2025 · The component that connects the recalled chandelier light fixture to the ceiling mount is not threaded properly and the fixture can fall unexpectedly, posing a... - TopHomer Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold on Amazon by TopHomerUS
Consumer productReported December 18, 2025 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Furnulem 8-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Furnulem
Consumer productReported December 18, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injuries or death to... - Pedego Electric Bikes Recalls Fat Tire Trikes Due to Fall and Laceration Hazards
Consumer productReported December 18, 2025 · The trike frame can develop a hairline fracture near a weld, which can cause the tubes to separate, posing fall and laceration hazards. - Pacific Cycle Recalls Schwinn Ovation Bicycle Child Carriers Due to Fall Hazard
Consumer productReported December 18, 2025 · The buckles securing the restraints around the child can release during use, posing a fall hazard. - Amp Fit Recalls AMP Smart Fitness Machines Due to Laceration and Serious Injury Hazard
Consumer productReported December 18, 2025 · The arm on the MP2 model of the fitness machine does not lock properly, which can allow the arm to swing unexpectedly, posing a risk of laceration or serious... - Outer-packaging: gimme! brand Decaf de Agua coffee pods recall (Gimme Coffee, Inc.)
FoodClass IIReported December 17, 2025 · Undeclared caffeine - Doughy brand Chocolate Chip Cookie Dough recall (HUDSON RIVER FOODS CORP)
FoodClass IReported December 17, 2025 · Product may be contaminated with Salmonella - AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product... recall (Steris Corporation)
Medical deviceClass IIReported December 17, 2025 · Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within... - AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description:... recall (Steris Corporation)
Medical deviceClass IIReported December 17, 2025 · Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within... - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Morphine Sulfate Oral Solution 100 mg / 5 mL recall (Winder Laboratories, LLC)
DrugClass IIIReported December 17, 2025 · Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton. - Nebivolol Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIReported December 17, 2025 · Cross Contamination with Other Products - Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic... recall (Fagron Compounding Services)
DrugClass IIReported December 17, 2025 · Incorrect Product Formulation - Luyuan Recalls Youth ATVs Due to Risk of Serious Injury or Death from Crash Hazard; Violate Mandatory Standard for All-Terrain Vehicles
Consumer productReported December 11, 2025 · The recalled youth ATVs violate the mandatory ATV safety standard. The youth ATVs' mechanical suspension fails to comply with safety requirements, posing a... - Sanven Technology Recalls Vevor Ice Crushers Due to Fire Hazard
Consumer productReported December 11, 2025 · The ice crusher can experience a thermal event and ignite, posing a fire hazard. - YCXXKJ Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats; Sold on Amazon by BenTalk
Consumer productReported December 11, 2025 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious... - Sanven Technology Recalls VEVOR Steamers Due to Risk of Serious Injury from Burn Hazard
Consumer productReported December 11, 2025 · The steamers can leak or spit hot water, posing a risk of serious burn injury to users and bystanders. The water tank cap can also leak or detach during use... - Uuoeebb Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by BaoD
Consumer productReported December 11, 2025 · 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... - SKCAIHT Children's Costumes Recalled Due to Risk of Injury from Phthalate Exposure; Violates Federal Phthalates Ban; Sold on Amazon by SKCAIHT Direct
Consumer productReported December 11, 2025 · The children's costumes contain a prohibited phthalate, which violates the federal phthalates ban. Phthalates are toxic if ingested by young children and can... - Primark Recalls Little Bear 2-Pack Soother Clips Due to Choking and Laceration Hazards
Consumer productReported December 11, 2025 · The wooden button on the soother clips can come off, exposing a sharp screw, which can pose choking and laceration hazards. - TREK Recalls Electric Bicycles Due to Fall or Crash Hazard
Consumer productReported December 11, 2025 · The bolts on the chainring can come loose, causing the chainring to separate from the bike, resulting in a fall or crash hazard to the user. - Lava Bun with Salted Egg Yolk orange packaging recall (Prime Food Processing LLC.)
FoodClass IIReported December 10, 2025 · Products do not declare milk in the Contains statement or the ingredient statement. - Lava Bun with Green Tea Flavor bright lime green packaging recall (Prime Food Processing LLC.)
FoodClass IIReported December 10, 2025 · Products do not declare milk in the Contains statement or the ingredient statement. - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported December 10, 2025 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported December 10, 2025 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Bisoprolol Fumarate and Hydrochlorothiazide Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIReported December 10, 2025 · Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe - INIU Recalls Power Banks Due to Fire and Burn Hazards; Sold on Amazon
Consumer productReported December 5, 2025 · The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers. - Grizzly Industrial Recalls Heavy-Duty Planers Due to Impact and Laceration Hazards
Consumer productReported December 4, 2025 · The chip breaker can contact the cutterhead blades during use, which can cause debris to be ejected from the planer, posing impact and laceration hazards to... - Cubimana Building Toy Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Shein by Vatos Toys
Consumer productReported December 4, 2025 · The building toy sets violate the mandatory safety standard because the battery compartment within the LED light piece contains button cell batteries that can... - Little Pea Shop Crib Bumpers Recalled Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban; Sold by Little Pea Shop
Consumer productReported December 4, 2025 · The recalled crib bumpers violate the federal crib bumper ban because they can obstruct an infant's breathing, posing a risk of serious injury or death, due to... - KTEBO Writing Tablet Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by KTEBO
Consumer productReported December 4, 2025 · The recalled toys violate the mandatory standard for toys because the screw used to secure the battery compartment that contains a button cell battery does not... - HydroJug Recalls 14-Ounce Children's Sport Tumblers Due to Choking Hazard
Consumer productReported December 4, 2025 · The rivets on the handle can come loose, causing the handle to detach, posing a choking hazard for children. - CreateOn Recalls Pip-Cubes Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard
Consumer productReported December 4, 2025 · The recalled magnetic building cubes contain magnets that can become loose if the seams separate, posing an ingestion hazard to children. When high-powered... - Casaottima 13-Drawer 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 Amazon by Casaottima
Consumer productReported December 4, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries... - Ningbo Tianqi Electronic Recalls FUFU&GAGA Murphy Wall Beds Due to Impact and Laceration Hazards
Consumer productReported December 4, 2025 · During assembly or disassembly, the 215-pound frame of the wall bed can fall onto consumers, posing deadly impact, crush, and laceration hazards. - Primark US Recalls Primark Water Balloon Pumps Due to Injury Hazard
Consumer productReported December 4, 2025 · The water balloon pump can generate excessive pressure during use, causing the product to rupture, posing a risk of physical injury to the user or bystanders. - McLee Creations Recalls MyOnlyStyler Root Booster Hair Dryers Due to Risk of Serious Injury or Death from Electrocution and Shock Hazards
Consumer productReported November 26, 2025 · The handheld hair dryers lack an immersion protection device, which presents a substantial product hazard to consumers, posing the risk of death or serious... - Outdoor Master Children's and Youth Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold and Imported by Outdoor Master
Consumer productReported November 26, 2025 · The recalled children's and youth helmets violate the mandatory safety standard for bicycle helmets. Particularly, the helmets do not comply with the... - Convertible High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for High Chairs; Sold on Amazon by Rotinyard
Consumer productReported November 26, 2025 · The high chairs violate the mandatory standard for high chairs because they were sold without the required attached restraint system, posing a deadly fall... - Ozark Trail Tabletop 1-Burner Butane Camping Stoves Recalled Due to Serious Burn and Fire Hazards; Imported and Sold by Walmart; Manufactured by China Window Industry Co.
Consumer productReported November 26, 2025 · The stoves can explode or catch fire, posing a burn and fire hazard to consumers. - Sofoliana and Glotika Baby Loungers Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products; Sold on Amazon by Bosen US
Consumer productReported November 26, 2025 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed...