Recalls in North Dakota (page 38)
3825 recalls.
- NFSVLB Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning and Entrapment; Violate Mandatory Standard for Infant Bath Seats; Sold on Amazon by NFSVLB
Consumer productReported January 9, 2026 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, and have leg openings... - Marcus Adler Glove Recalls Julie and Judah Pajama Pants and Shorts Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported January 9, 2026 · The pajama pants and shorts violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children. - The Kalencom Corporation Recalls SARO Braided Crib Bumpers Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban
Consumer productReported January 9, 2026 · The recalled padded crib bumpers violate the federal ban on crib bumpers because they can obstruct an infant's breathing, posing a risk of serious injury or... - Infant Innovations Recalls BabyBond Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported January 9, 2026 · 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... - DR Power Equipment Reannounces and Expands Recall of Leaf Vacuums Due to Laceration Hazard; New Remedy Available
Consumer productReported January 9, 2026 · Pieces from the recalled leaf vacuums can come loose inside the unit, or debris can pierce the chute, resulting in material ejecting and posing a laceration... - Agrish 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; Sold on Amazon by Agrish Direct
Consumer productReported January 9, 2026 · 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... - Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Chocolate GF V. Product is... recall (Tom Bumble LLC)
FoodClass IIReported January 7, 2026 · Foreign material. - traZODONE Hydrochloride Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIIReported January 7, 2026 · Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface. - Ondansetron Orally Disintegrating Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported January 7, 2026 · Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets... - Wegovy recall (Novo Nordisk Inc.)
DrugClass IIReported January 7, 2026 · Presence of Particulate Matter: Hair was found in a prefilled syringe - Wegovy recall (Novo Nordisk Inc.)
DrugClass IIReported January 7, 2026 · Presence of Particulate Matter: Hair was found in a prefilled syringe - BD ChloraPrep" Triple Swabsticks recall (CareFusion 213, LLC)
DrugClass IIReported January 7, 2026 · Lack of Assurance of Sterlity - BVI Leos Laser and Endoscopy System. Model Number: OME6000U. recall (Beaver-Visitec International, Inc.)
Medical deviceClass IIReported January 7, 2026 · Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not... - Sheathes3D Seamless Viral Barrier recall (Sheathing Technologies Inc)
Medical deviceClass IIReported January 7, 2026 · Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk. - Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog... recall (Ferndale Laboratories, Inc.)
Medical deviceClass IIReported January 7, 2026 · Butyrate tube cracks during actuation, rendering product unusable. - Product: Zimi Kunefe Ready to eat recall (Karabetian Import and Distribution, Inc.)
FoodClass IIReported December 31, 2025 · partially hydrogenated oils (PHOs) in foods exported to the US - Product: Zimi Puff Pastry French Style recall (Karabetian Import and Distribution, Inc.)
FoodClass IIReported December 31, 2025 · partially hydrogenated oils (PHOs) in foods exported to the US - 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... - Brand Name: Alcon Laboratories recall (Alcon Research LLC)
Medical deviceClass IReported December 31, 2025 · Ophthalmic procedure packs may have incomplete seals affecting sterility. - 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. - 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... - 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... - 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. - 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... - 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... - 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 - BIOSURE HA SCREW recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported December 24, 2025 · Removal of affected lot of screws due to labeling error. - 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... - Simplot¿ Traditional Reduced Sodium Tater Gems¿ recall (JR Simplot Company)
FoodClass IIReported December 17, 2025 · Plastic fragments. Pieces of semi-rigid plastic embedded in the recalled Tater Gems product. - 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 - 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... - 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. - 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...