Recalls in North Dakota (page 23)
3825 recalls.
- 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... - 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... - Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID:... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported May 20, 2026 · Out-of-specification endotoxin result that did not meet the acceptance criteria. - Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO recall (Edwards Lifesciences, LLC)
Medical deviceClass IIReported May 20, 2026 · Labeling update to provide warning if functionality of the valve replacement delivery system is compromised. - 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... - 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 - CS Uni-Directional w Auto ID recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - CS Uni-Directional w Auto ID recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BW Webster Duo-Decapolar recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD EP XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD EP XT Decapolar Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Deca Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Deca Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - ZYMUTEST HIA IgG recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported May 20, 2026 · Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the... - Philips Azurion. System Code Description recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 20, 2026 · Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over... - QuickVue Dipstick Strep A Test recall (Quidel Corporation)
Medical deviceClass IIReported May 20, 2026 · Product has the potential for false positive results - 3DIMENSIONS MAMMOGRAPHY SYSTEM recall (Hologic, Inc)
Medical deviceClass IIReported May 20, 2026 · Complaints have been received of systems developing loose, missing, or broken internal bolts over time. - SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC recall (Hologic, Inc)
Medical deviceClass IIReported May 20, 2026 · Complaints have been received of systems developing loose, missing, or broken internal bolts over time. - Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The... recall (Stryker Corporation)
Medical deviceClass IIReported May 20, 2026 · Due to nonconforming products being inadvertently distributed. - Diowave Laser System recall (Technological Medical Advancements LLC)
Medical deviceClass IIReported May 20, 2026 · Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness... - 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... - NextStep Antegrade Chronic Hemodialysis Catheter recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported May 20, 2026 · 16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not... - Cannon II Plus Hemodialysis Catheter recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported May 20, 2026 · 16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not... - Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported May 20, 2026 · 16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not... - Arrow Edge Hemodialysis Catheterization Product recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported May 20, 2026 · 16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not... - Revolution Apex Select recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Apex recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution CT ES recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Apex Plus recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Apex Elite recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution CT recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Ascend recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - 1. 3 VALVE MAN KIT recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - 1. DBD-MTS recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Preceptor Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Preceptor Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Angiographic Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Angiographic Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Angiographic Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Brand Name: DONJOY Product Name: ICEMAN recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Brand Name: DONJOY Product Name: ICEMAN W/ recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Brand Name: DONJOY Product Name: ICEMAN W/ recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 ... recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes... recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported May 20, 2026 · Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which... - Generac Power Systems Expands Recall of Generac and DR Power Electric Start Pressure Washers Due to Risk of Serious Injury or Death from Carbon Monoxide Hazard; Includes Additional Models
Consumer productReported May 15, 2026 · The electronic start/stop button on the pressure washer can malfunction and self-start, posing a risk of serious injury or death due to carbon monoxide... - Cosyland Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Cosyland Official
Consumer productReported May 15, 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... - Guidecraft Children's Standing Towers Recalled Due to Risk of Serious Injury from Fall Hazard
Consumer productReported May 15, 2026 · The platform inside the recalled tower can loosen over time, causing it to become unstable or detach, and ultimately posing a fall hazard to young children. - ZWILLING J. A. Henckels Aktiengesellschaft Recalls Electric Water Kettles Due to Risk of Serious Injury Due to Burn Hazard
Consumer productReported May 15, 2026 · The kettle's handle can loosen and separate from the kettle, causing hot contents to spill, posing a risk of serious injury due to a burn hazard. - Petzl America Recalls ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE Harnesses Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported May 15, 2026 · The recalled harness' D-ring can release, allowing the attachment point to open, posing a risk of serious injury or death from a fall hazard. - Petzl America Recalls SIMBA and SWAN EASYFIT Harnesses Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported May 15, 2026 · The recalled harnesses are missing rivets in the FAST LT PIN-LOCK buckles, causing the buckles to open, posing a risk of serious injury or death from a fall... - Amazon Recalls Amazon Basics 55 Lbs. Adjustable Dumbbells Due to Impact Hazard
Consumer productReported May 15, 2026 · The weight plates can fail to engage completely during weight adjustment and dislodge from the dumbbell handle when used, posing an impact hazard. - World Bright International Limited Recalls Agio Menlo Woven Patio Swings Due to Risk of Serious Injury or Death from Fall Hazard; Sold at Costco
Consumer productReported May 15, 2026 · The swing seat can detach from the frame while in use, posing a risk of serious injury or death from a fall hazard. - Lithium Coin Batteries Recalled Due?to Risk of Serious Injury or Death from Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported and Sold on Amazon by LiCB
Consumer productReported May 15, 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... - Missry Associates Recalls Misco Sports Badminton Toy Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
Consumer productReported May 15, 2026 · The Misco Sports Badminton Toy Sets violate the mandatory safety standard for children's toys because the shuttlecocks contain button cell batteries that can... - BRP Recalls Can-Am All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury and Death from Crash Hazard
Consumer productReported May 15, 2026 · The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard. - Tiyol Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violates Mandatory Standard for Toys; Sold on Amazon by ZW Creations
Consumer productReported May 15, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can... - Superbobi Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Manufactured by Remy&shop
Consumer productReported May 15, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Minka Lighting Group Recalls Bardon Series Pendant Light Fixtures Due to Risk of Serious Injury or Death from an Impact Hazard
Consumer productReported May 15, 2026 · The recalled light fixture's frame can detach from the pendant downrod during installation, posing a risk of serious injury or death from an impact hazard.