Recalls in Hawaii (page 23)

3886 recalls.

• Joy Furniture Recalls Talan and Royce Living Room Furniture Sets Due to Risk of Serious Injury from a Fire Hazard
  Consumer productReported May 28, 2026 · The power switch on the sofa, loveseat, or recliner can malfunction and overheat posing a risk of serious injury from a fire hazard.
• Giantex Recalls Lounge Chairs Due to Amputation Hazard
  Consumer productReported May 28, 2026 · Consumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk.
• Tzumi Electronics Recalls SLF Sauna Blankets Due to Fire and Burn Hazards
  Consumer productReported May 28, 2026 · The recalled sauna blankets can overheat, posing fire and burn hazards.
• Lithium Coin Batteries Recalled Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported by Proudly American Store, of Canada
  Consumer productReported May 28, 2026 · The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. When button cell or coin...
• Daoen Recalls Zen Magnetic Promotional Ball Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
  Consumer productReported May 28, 2026 · The recalled magnetic balls violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When...
• MiniWarGaming and Primal Horizon Disc Magnets Recalled Due to Risk of Serious Injury or Death from Ingestion; Violate Mandatory Standard for Magnets; Imported by MiniWarGaming
  Consumer productReported May 28, 2026 · The magnets violate the mandatory safety standard for magnets because the high-powered magnets fit within CPSC's small parts cylinder and are stronger than...
• Giantex Recalls Giantex and Costway Portable Steam Saunas Due to Burn Hazard
  Consumer productReported May 28, 2026 · The sauna's steam diffuser can be positioned too close to a consumer's body, allowing hot steam to come in contact with user, posing a burn hazard.
• Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 ... recall (C.R. Bard Inc)
  Medical deviceClass IIReported May 27, 2026 · Due to stain present on the surface of affected foley catheters.
• Swan-Ganz Pacing Catheter recall (Becton, Dickinson and Company)
  Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection...
• Swan-Ganz Jr Catheter recall (Becton, Dickinson and Company)
  Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection...
• Swan-Ganz Catheter recall (Becton, Dickinson and Company)
  Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection...
• Fisher Tex Mex Trail Mix 30 oz plastic jar recall (JOHN B SANFILIPPO & SONS INC)
  FoodClass IReported May 27, 2026 · potential presence of Salmonella
• Good & Gather Mexican Street Corn Trail Mix 8 oz bag recall (JOHN B SANFILIPPO & SONS INC)
  FoodClass IReported May 27, 2026 · potential presence of Salmonella
• Squirrel Brand Town & Country Mix 16 oz can recall (JOHN B SANFILIPPO & SONS INC)
  FoodClass IReported May 27, 2026 · potential presence of Salmonella
• Squirrel Brand Travelers Mix 16 oz can recall (JOHN B SANFILIPPO & SONS INC)
  FoodClass IReported May 27, 2026 · potential presence of Salmonella
• Southern Style Nuts Hunter Mix 30 oz plastic jar recall (JOHN B SANFILIPPO & SONS INC)
  FoodClass IReported May 27, 2026 · potential presence of Salmonella
• Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar recall (JOHN B SANFILIPPO & SONS INC)
  FoodClass IReported May 27, 2026 · potential presence of Salmonella
• Non Fat Dry Milk 1# recall (PS Seasoning & Spices, Inc.)
  FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.
• PSW21585 Save A Lot Bind 50# recall (PS Seasoning & Spices, Inc.)
  FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.
• Blackstone Parmesan Ranch Seasoning recall (PS Seasoning & Spices, Inc.)
  FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.
• 1P Jalapeno Heat Unit for 300 lbs of Meat recall (PS Seasoning & Spices, Inc.)
  FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.
• 1P Original Smokehouse Unit for 300 lbs. of Meat recall (PS Seasoning & Spices, Inc.)
  FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.
• Ellsworth Sour Cream + Onion Seasoning recall (PS Seasoning & Spices, Inc.)
  FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.
• Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid.... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml.... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging:... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging:... recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• FulviLife Complex. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
• Joint Nourish. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
  FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.
• MG217 Multi-Symptom Treatment Cream & Skin Protectant recall (Wisconsin Pharmacal Company)
  DrugClass IReported May 27, 2026 · Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
• fentaNYL Citrate recall (IntegraDose Compounding Services LLC)
  DrugClass IIReported May 27, 2026 · Subpotent Drug
• cimzia recall (UCB Biosciences Inc.)
  DrugClass IIReported May 27, 2026 · Lack of Assurance of Sterility
• Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)
  DrugClass IIReported May 27, 2026 · CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
• Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)
  DrugClass IIReported May 27, 2026 · CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
• Estradiol Gel recall (ANI Pharmaceuticals, Inc.)
  DrugClass IIReported May 27, 2026 · Defective Container; packets were found to be either empty or partially full.
• Gas-X recall (Haleon US Holdings LLC)
  DrugClass IIReported May 27, 2026 · Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.
• Liraglutide Injection recall (Lupin Pharmaceuticals Inc.)
  DrugClass IIReported May 27, 2026 · Presence of particulate matter: a white thread-like structure in the cartridge
• Busulfan Injection recall (Sagent Pharmaceuticals)
  DrugClass IIIReported May 27, 2026 · Failed Impurities/Degradation Specifications
• Primidone Tablets recall (Amerisource Health Services LLC)
  DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
• Primidone Tablets recall (Amerisource Health Services LLC)
  DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
• Primidone Tablets recall (Golden State Medical Supply Inc.)
  DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
• Primidone Tablets recall (Golden State Medical Supply Inc.)
  DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
• Primidone Tablets USP recall (Lannett Company Inc.)
  DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
• Integris-Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in...
• Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in...
• Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in...
• Philips Azurion systems not configured with an optional auxiliary pan handle. Includes... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported May 27, 2026 · Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float...
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
  Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.
• OneLIF Interbody Cage recall (Novapproach Spine, LLC)
  Medical deviceClass IIReported May 27, 2026 · Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the...
• Oncology Kit w/60" recall (ICU Medical, Inc.)
  Medical deviceClass IIReported May 27, 2026 · Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak...
• Tangent Endoscopy recall (TANGENT ENDOSCOPY, LLC)
  Medical deviceClass IIReported May 27, 2026 · Affected devices exhibited fractures at the distal shaft tip without complete detachment.
• Bethlehem Lights Recalls Bethlehem Lights 10-inch Illuminated Ribbon Spheres Due to Risk of Serious Injury or Death from Fire Hazard; Sold by QVC
  Consumer productReported May 26, 2026 · The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.
• ABC Trading Recalls WSDZ Light-up Glasses Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
  Consumer productReported May 26, 2026 · The recalled glasses violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries can be accessed...
• PandaEar Recalls Portable Hook-On Chairs Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Portable Hook-On Chairs
  Consumer productReported May 26, 2026 · The recalled portable hook-on chairs violate the mandatory standard for portable hook-on chairs because the crotch restraints can be removed without the use of...
• Lil Pick Up Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash and Burn Hazards; Violates Mandatory Standard for ATVs
  Consumer productReported May 26, 2026 · The recalled youth ATVs violate the federal mandatory ATV safety standard, posing a risk of serious injury or death. The youth ATVs fail to meet mechanical...
• Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory
  Consumer productReported May 26, 2026 · The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.
• Resistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym
  Consumer productReported May 26, 2026 · The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.
• ABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
  Consumer productReported May 26, 2026 · The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries...
• Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom... recall (Dexcom, Inc.)
  Medical deviceClass IIReported May 20, 2026 · A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend...
• Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7... recall (Dexcom, Inc.)
  Medical deviceClass IIReported May 20, 2026 · A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend...
• Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7... recall (Dexcom, Inc.)
  Medical deviceClass IIReported May 20, 2026 · A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend...
• LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI... recall (Jolife AB)
  Medical deviceClass IIReported May 20, 2026 · Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the...
• Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original -... recall (Dakota Honey Company)
  FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic)
• Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
  FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic)
• Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
  FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic)
• Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
  FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic)
• Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
  FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic)
• Ascend Laboratories recall (Ascend Laboratories, LLC)
  DrugClass IIReported May 20, 2026 · Failed Dissolution Specifications
• Buprenorphine Hydrochloride recall (ENDO USA, Inc.)
  DrugClass IIReported May 20, 2026 · Crystallization; identified as Buprenorphine free base
• Oasis Tears PF recall (Oasis Medical, Inc.)
  DrugClass IIReported May 20, 2026 · Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of...
• Medtronic Marinr Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable BDB recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product
• Daig Livewire Steerable recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product

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