Recalls in Utah (page 14)
3917 recalls.
- Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. ... recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. - Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog... recall (Prismatik Dentalcraft, Inc.)
Medical deviceClass IIReported July 29, 2026 · Due to device not having FDA Clearance - 3mensio Workstation recall (PIE Medical Imaging B.V.)
Medical deviceClass IIReported July 29, 2026 · User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than... - Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect concentration of Betadine solution contained within certain AVID convenience kits. - Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities. - Hotline Fluid Warming Set recall (ICU Medical Inc.)
Medical deviceClass IIReported July 29, 2026 · ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent... - P28 PHANTON INTRAMEDULLARY NAIL SYSTEM recall (Paragon 28, Inc.)
Medical deviceClass IIReported July 29, 2026 · Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging. - FARADRIVE STEERABLE SHEATH CLEAR OUS recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE STEERABLE SHEATH recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE STEERABLE SHEATH CLEAR recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE Steerable Sheath Clear IDE recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - The intended use is to be paired with a weapon for aiming purposes. recall (Wilcox Industries Corp.)
Medical deviceClass IIReported July 29, 2026 · Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all... - Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported July 24, 2026 · The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children. - CuddleCubs Creations Teething Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by YouRfocus
Consumer productReported July 24, 2026 · The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and... - OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold Exclusively on Amazon by Yuanxinxiang
Consumer productReported July 24, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act
Consumer productReported July 24, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Aojieni Silicone Recalls Sili Factory Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
Consumer productReported July 24, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - 12-Drawer Fabric 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 Romorgniz
Consumer productReported July 24, 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... - EnHomee 9-Drawer Fabric 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 Walmart.com by Raybee-Direct
Consumer productReported July 24, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or... - functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA... recall (Nutricia North America)
FoodClass IIReported July 22, 2026 · Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher... - functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE... recall (Nutricia North America)
FoodClass IIReported July 22, 2026 · Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Orthofix MINIRAIL recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111 recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - Orthofix MINIRAIL recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - Orthofix MINIRAIL recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 22, 2026 · Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator - CLEVIPREX recall (Chiesi USA, Inc.)
DrugClass IIReported July 22, 2026 · Lack of Assurance of Sterility - CAREone recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - meijer recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - Foster & Thrive recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - LEADER recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - GOOD NEIGHBOR PHARMACY recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - FAMILY Wellness recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - AUDIOLOGIST'S CHOICE recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - TopCare Health recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - QC Quality Choice recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - Clinere recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - CVS Health recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - Nystatin Cream USP recall (Padagis US LLC)
DrugClass IIReported July 22, 2026 · Subpotent Drug: Low out of specification assay results performed during long-term stability testing. - ST AIA-Pack Testosterone recall (Tosoh Bioscience Inc)
Medical deviceClass IIReported July 22, 2026 · The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could... - Photera 600 3-D recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - Photera 600 recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - Photera 400 recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recall (Maquet Cardiovascular, LLC)
Medical deviceClass IIReported July 22, 2026 · Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization... - Medtronic Bio-Medicus Adult Cannula Kit recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Medtronic DLP One-Piece Pediatric Arterial Cannula recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Papablic Replacement Brush Heads. Model Number: PAPA317AA. recall (Papablic Inc)
Medical deviceClass IIReported July 22, 2026 · Potential for brush heads to break. - Papablic Replacement Brush Heads. Model Number: Papablic18B recall (Papablic Inc)
Medical deviceClass IIReported July 22, 2026 · Potential for brush heads to break. - Optima XR240amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Optima XR220amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Optima XR200amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Rapid Refill Continuous Injection System recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 22, 2026 · Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the... - ICU Medical Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - ICU Medical Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Ellik Evacuator Includes Glass Body recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Arterial Line Kit 20ga x 6 recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - T-Lok Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - General Biospy Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - One-Piece Introducer Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - ABIOMED Intro Kit recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Insertion Kit recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Smart Assist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella 5.5 SmartAssist S2 Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella 5.5 Smart Assist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Introducer Kit 23 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella RP Flex with SmartAssist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - MNIENT 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
Consumer productReported July 17, 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... - Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported July 17, 2026 · The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard. - SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
Consumer productReported July 17, 2026 · The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of... - Noerishia Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Hurzein
Consumer productReported July 17, 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... - Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
Consumer productReported July 17, 2026 · The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of... - Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
Consumer productReported July 17, 2026 · The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death. - Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
Consumer productReported July 17, 2026 · The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning. - Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning
Consumer productReported July 17, 2026 · The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or... - Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
Consumer productReported July 17, 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... - Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard
Consumer productReported July 17, 2026 · The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard. - TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards
Consumer productReported July 17, 2026 · The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards. - Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo Technology
Consumer productReported July 17, 2026 · The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act.... - Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
Consumer productReported July 17, 2026 · The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard. - Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
Consumer productReported July 17, 2026 · The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children.... - Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough recall (Bear Stewart Co)
FoodClass IIReported July 15, 2026 · undeclared soy - TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia... recall (Think Surgical, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. - Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator ... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Intracept Access Instruments recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported July 15, 2026 · Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if...