Recalls in October 2026
96 recalls.
- Riad's Oliva to Go Hummus recall (Oliva on Main)
FoodClass IReported November 4, 2026 · contains undeclared sesame - Riad's Oliva to Go Spicy Baba Ghanouj recall (Oliva on Main)
FoodClass IReported November 4, 2026 · contains undeclared sesame - Riad's Oliva to Go Baba Ghanouj recall (Oliva on Main)
FoodClass IReported November 4, 2026 · contains undeclared sesame - EDEN BROTHERS Broccoli Seeds - Calabrese. Sold in packets recall (EDEN BROTHERS)
FoodClass IReported November 4, 2026 · Salmonella - Atorvastatin Calcium Tablets recall (MSN Laboratories Private Limited (Formulations Division, Unit-II))
DrugClass IIReported November 4, 2026 · Presence of Foreign Tablets/Capsules - Theophylline Extended-Release Tablets recall (Brandywine Pharmaceuticals, LLC)
DrugClass IIReported November 4, 2026 · CGMP Deviations: interruption in the ongoing stability testing program conducted at a third-party laboratory - Theophylline Extended-Release Tablets recall (Brandywine Pharmaceuticals, LLC)
DrugClass IIReported November 4, 2026 · CGMP Deviations: interruption in the ongoing stability testing program conducted at a third-party laboratory - Vecuronium Bromide for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIIReported November 4, 2026 · Labeling: Label Lacks Warning or Rx Legend - Vecuronium Bromide for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIIReported November 4, 2026 · Labeling: Label Lacks Warning or Rx Legend - OXYTOCIN recall (Eagle Pharma Outsourcing LLC)
DrugClass IIReported November 4, 2026 · Lack of Assurance of Sterility - PHENYLephrine HCL Infusion recall (Eagle Pharma Outsourcing LLC)
DrugClass IIReported November 4, 2026 · Lack of Assurance of Sterility - ULTRA STRENTGH recall (Fei Fah Medical Manufacturing Pte. Ltd.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg recall (Prodose, Inc.)
DrugClass IIIReported November 4, 2026 · Incorrect label placed on product: Outer carton label correctly identifies drug product in bottle as ValuHealth Extra Strength Pain Relief Acetaminophen 500... - Carboxymethylcellulose Sodium recall (Huons Co., Ltd.)
DrugClass IIReported November 4, 2026 · Failed Impurities/Degradation Specification; detection of polyethylene (PE)-related oligomers - Olmesartan Medoxomil recall (MACLEODS PHARMA USA, INC)
DrugClass IIReported November 4, 2026 · Failed Dissolution Specifications. - Metoclopramide Tablets recall (Safecor Health, LLC)
DrugClass IIReported November 4, 2026 · Manufacturer is recalling batches due to co-mingled tablet. - Abiraterone Acetate Tablets USP 500 mg recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported November 4, 2026 · Labeling: Not Elsewhere Classified - Formoterol Fumarate Inhalation Solution recall (The Ritedose Corporation)
DrugClass IIReported November 4, 2026 · Failed Impurities/Degradation Specification - Philips Azurion S. Model Number: 722285. recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 7 M20. Model Numbers: 722079 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 7 M12. Model Numbers: 722078 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 7 B20. Model Numbers: 722068 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 7 B12. Model Numbers: 722067 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 5 M20. Model Numbers: 722228 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 5 M12. Model Number: 722227. recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 3 M15. Model Number: 722064 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - Philips Azurion 3 M12. Model Numbers: 722063 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported November 4, 2026 · Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance... - ALPHENIX INTERVENTIONAL ANGIOGRAPHY SYSTEM REF: INFX-8000V recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported November 4, 2026 · Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis... - ALPHENIX INTERVENTIONAL ANGIOGRAPHY SYSTEM REF: INFX-8000F recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported November 4, 2026 · Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis... - ALPHENIX INTERVENTIONAL ANGIOGRAPHY SYSTEM REF: INFX-8000C recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported November 4, 2026 · Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis... - Longjili Trading Recalls Pamag Pieeoo Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability
Consumer productReported October 29, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - Harkla Recalls Children’s Sensory Swings Due to Risk of Serious Injury from Fall Hazard
Consumer productReported October 29, 2026 · The recalled swings’ ceiling hook can separate from its plate, posing a risk of serious injury from a fall hazard. - Yinklev Recalls Jocoevol 6-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported October 29, 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... - RootStim Recalls Minoxidil Hair Regrowth Treatment Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported October 29, 2026 · The recalled hair regrowth products contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The... - HAIARA Power Banks Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Sold on Amazon.com by Mitrytech
Consumer productReported October 29, 2026 · The power bank’s lithium battery can explode and ignite, posing fire and burn hazards to consumers. - Bodum USA Recalls 5.9 Million French Press Coffee Makers with Replaceable Glass Carafes Due to Risk of Serious Burn Injury
Consumer productReported October 29, 2026 · The carafe can unexpectedly break during use if the glass carafe is damaged or cracked, including by use of a metal spoon to stir the coffee, posing a risk of... - DREO Recalls DR-HSH015 Space Heaters Due to Fire and Burn Hazards
Consumer productReported October 29, 2026 · The recalled space heaters can overheat and ignite, posing fire and burn hazards. - NTI and HTP Brand Gas Boilers Recalled Due to Risk of Serious Injury or Death from Fire, Carbon Monoxide (CO) Poisoning and Impact Hazards; Manufactured by Ariston, formerly NTI Boilers
Consumer productReported October 29, 2026 · The condensate dish inside the boiler can crack during a delayed ignition, allowing unburned gas to build up inside the sealed cabinet. If the gas ignites, the... - Whatever Works Recalls Microwave Grills Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 29, 2026 · The recalled grills can overheat and ignite, posing a risk of serious injury or death from fire hazard. - SOOWERY Recalls 8-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported October 29, 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... - PILLANI Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows
Consumer productReported October 29, 2026 · The recalled nursing pillows violate the mandatory safety standards for nursing pillows because they can obstruct an infant’s breathing, posing a serious risk... - Fashion Brand Apparel Recalls QZH.DUAO Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standards for Children’s Sleepwear
Consumer productReported October 29, 2026 · The recalled children’s pajama sets violate the mandatory safety standards for children’s sleepwear, posing a risk of serious burn injuries. - Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed. Net wt. 8oz ASIN... recall (EAK Distribution LLC)
FoodClass IReported October 28, 2026 · Salmonella. - Babies' Magic Tea recall (Pacific Health Sciences Llc)
FoodClass IIReported October 28, 2026 · Adulterated (elevated levels of alcohol) infant dietary supplement - Great Value Fruit Cocktail in Fruit Juice from Concentrate recall (Pacific Coast Producers)
FoodClass IIReported October 28, 2026 · Potential contamination with elevated levels of lead. - Andronico's COMMUNITY MARKETS 100% SQUEEZED ORANGE ANDROINCO'S COMMUNITY MARKETS SAN... recall (Voila Juice Company)
FoodClass IIReported October 28, 2026 · Product not processed to achieve 5-log pathogen reduction. - Voila! juice 100% SQUEEZED ORANGE VOILA! OAKLAND recall (Voila Juice Company)
FoodClass IIReported October 28, 2026 · Product not processed to achieve 5-log pathogen reduction. - Glutathione Injection recall (Greenwich Rx)
DrugClass IReported October 28, 2026 · Microbial Contamination of Sterile Products - Argatroban Injection recall (Par Health USA, LLC)
DrugClass IReported October 28, 2026 · Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product... - Argatroban Injection recall (Par Health USA, LLC)
DrugClass IReported October 28, 2026 · Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product... - Cinacalcet Tablets recall (STRIDES PHARMA INC)
DrugClass IIReported October 28, 2026 · Failed dissolution specifications - Abirtega recall (Hikma Pharmaceuticals USA INC.)
DrugClass IIReported October 28, 2026 · Failed Tablet/Capsule Specifications: Failed tablet specifications for weight uniformity. - Testosterone Cypionate recall (Right Value Drug Stores LLC)
DrugClass IIReported October 28, 2026 · Lack of sterility assurance. - Heparin Sodium Injection recall (Shenzhen Techdow Pharmaceutical Co., Ltd.)
DrugClass IIReported October 28, 2026 · Lack of Assurance of Sterility - Telmisartan and Amlodipine recall (Viatris, Inc.)
DrugClass IIIReported October 28, 2026 · Superpotent Drug: potential for the Telmisartan content in these lots to exceed specifications - Amlodipine and Olmesartan Medoxomil Tablets recall (Ascend Laboratories, LLC)
DrugClass IIReported October 28, 2026 · Out of specification due to dissolution. - BAMAMON Recalls LED Projecting Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 22, 2026 · None reported. - Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arm Mountings Due to Risk of Serious Injury from Impact Hazard
Consumer productReported October 22, 2026 · The knuckle of the recalled adjustable tilt arm mountings can fail, allowing the luminaire to fall from the mounting arm, posing a risk of serious injury due... - Costway Recalls Convertible High Chairs Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs
Consumer productReported October 22, 2026 · The convertible high chairs violate the mandatory safety standard for high chairs because they do not contain a passive restraint system and a child can slip... - VQQQ Gas Patio Heaters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported October 22, 2026 · Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards. - FoShanShiNanHaiQuNuoAiTongZhuangShangHang Recalls CIYTI Light-Up Princess Costumes Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 22, 2026 · The costumes violate the mandatory safety standard for toys because the button cell batteries can be accessed easily by children, posing a deadly ingestion... - Pur Aqua Sparkling Frost Cherry Limeade 17 oz. recall (Refresco Beverages US Inc)
FoodClass IIIReported October 21, 2026 · May contain undeclared aspartame. - Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon recall (Stewart's Shops Corp.)
FoodClass IIReported October 21, 2026 · Foreign object: May contain pieces of metal - Stewarts Shops Vanilla chocolate Strawberry Ice Cream 1/2 gallon recall (Stewart's Shops Corp.)
FoodClass IIReported October 21, 2026 · Foreign object: May contain pieces of metal - Metoclopramide Tablets recall (American Health Packaging)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - Hydrocortisone Sodium Succinate for Injection recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported October 21, 2026 · Failed Impurities/Degradation Specifications. - usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported October 15, 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... - Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion
Consumer productReported October 15, 2026 · The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through... - Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards
Consumer productReported October 15, 2026 · The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby... - Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards
Consumer productReported October 15, 2026 · Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards. - HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard
Consumer productReported October 15, 2026 · The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from... - 3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 15, 2026 · The recalled thermal laminators can overheat, posing a fire hazard. - Saint Francis Apizza Frozen Supreme Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Saint Francis Apizza Frozen Mushroom & Onion Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Saint Francis Apizza Frozen Cheese Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Saint Francis Apizza Frozen Pepperoni Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - The Conqueror Recalls Avengers Medals Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets
Consumer productReported October 8, 2026 · The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to... - Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks Due to Risk of Serious Injury or Death from Burn and Fire Hazards
Consumer productReported October 8, 2026 · The fireplace's lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards. - Romorgniz Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported October 8, 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... - Pacearth Direct Recalls PACEARTH Swing Seats Due to Risk of Serious Injury from Fall Hazard
Consumer productReported October 8, 2026 · The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall... - ONTHEWEI Recalls Baby Bath Seats Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats
Consumer productReported October 8, 2026 · 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... - Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard
Consumer productReported October 8, 2026 · The recalled bicycles' front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard. - DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported October 8, 2026 · Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards. - Giant Bicycle Recalls LED-Light Keys Included with SureLock Bike Lock Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported October 8, 2026 · The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and... - Agrish Reannounces and Expands Recall of Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Additional Units Added
Consumer productReported October 1, 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... - Golden Resale Recalls Portable Camping Showers Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 1, 2026 · The recalled camping showers' immersion heaters can quickly ignite when they are partially or completely out of water, posing a risk of serious injury or death... - Dollar Tree Stores Recalls Electric Balloon Pumps Due to Burn Hazard
Consumer productReported October 1, 2026 · The recalled electric balloon pumps can overheat, posing a burn hazard. - Kobayashi Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported October 1, 2026 · The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn... - Walmart Recalls Over 4.4 Million Expert Grill Brushes Due to Ingestion Hazard
Consumer productReported October 1, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Gobi Heat Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported October 1, 2026 · The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn... - GBYMIUY Recalls Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 1, 2026 · The magnetic stick figure toy sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to... - Designs Direct Recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported October 1, 2026 · When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn... - LLK Trading Recalls Mochi Malrang Mystery Dumpling Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 1, 2026 · The mystery dumpling toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a... - YunHeng Recalls LandTale Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported October 1, 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... - Gazelle USA Recalls Urban Arrow Cargo Electric Bikes Due to Fall Hazard
Consumer productReported October 1, 2026 · The front bolt in the seat post clamping mechanism can break, causing the seat to become loose, posing a fall hazard. - ABC Trading Recalls Squishy Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 1, 2026 · The squishy toys violate the mandatory safety standard for toys because the water beads inside the toys expand larger than permitted, posing a deadly ingestion...