State

North Dakota product recalls

73,576 recalls have nationwide distribution and so reach North Dakota. 2,925 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total: 2,925
Critical: 265
Severe: 869
Most recent: 2026-10-14

Of the 2,925 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 869 (30%) are Severe.

Which agencies issued them

These figures cover only the 2,925 recalls whose distribution notice names North Dakota specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26251–26275 of 76501

HighFDA (Devices)·Z-1455-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik Inc is recalling 658 ITREVIA 7 implantable defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ITREVIA 7, DR-T QP DF-1, REF 392412, UDI: 04035479128807 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21119·2021-04-28
Pentair Recalls StaRite and Mastertemp Pool Heaters Due to Fire Hazard
Pentair Water Pool and Spa is recalling about 4,700 StaRite and Mastertemp pool heaters because a connection can leak a combustible air-gas mixture, posing a fire hazard.
Product
StaRite and Mastertemp pool heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V298000·2021-04-28
2021 BMW 330E Seat Belt Buckle Assembly Bolt Not Properly Secured
BMW is recalling certain 2021 330E, 330i, M340i, and M3 vehicles due to an undertightened bolt on the front seat belt buckle assembly. The defect may prevent proper occupant restraint, increasing injury risk.
Product
BMW — BMW M340I, 330I, 330E, M3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V300000·2021-04-28
Blue Bird Recalls 2018-2021 School Buses for Power Steering Defect
Blue Bird is recalling 2018-2021 Vision and All American school buses because an electrical issue may cause a loss of power steering, increasing crash risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, ALL AMERICAN, VISION, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2021·2021-04-28
Smiths Medical Recalls Tubing Components Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of tubing components for blood-pressure transducers due to insufficient or incomplete welds.
Product
Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1449-2021·2021-04-28
BIOTRONIK IPERIA 7 ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling 3,832 IPERIA 7 ICDs and CRT-Ds due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK IPERIA 7,VR-T, DX, DF-1, ProMRI, REF 393032, UDI: 04035479129477 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1456-2021·2021-04-28
Biotronik ILIVIA 7 ICD Recall for Premature Battery Depletion
Biotronik is recalling 3,497 ILIVIA 7 implantable cardioverter defibrillators due to a potential for premature battery depletion. The recall covers units distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, DR-T DF4 ProMRI, REF 404623, UDI: 04035479142100 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2021·2021-04-28
Biotronik Iperia 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 1,652 Iperia 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK Iperia 7, DR-T, DF-1, ProMRI REF 392409, UDI: 04035479128777 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1441-2021·2021-04-28
BIOTRONIK Ilestro 7 DR-T ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling Ilestro 7 DR-T implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK Ilestro 7 DR-T, DF-1, REF383562, UDI: 04035479125189 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1478-2021·2021-04-28
Smiths Medical Recalls Medex High Pressure Tubing Due to Weld Defects
Smiths Medical ASD Inc. is recalling specific lots of Medex high pressure tubing and components due to insufficient or incomplete welds.
Product
HIGH PRESSURE TUBING, 72IN, Model Number MX152114 (Component). Stopcocks and manifolds are used to control the direction of IV fluid flow.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2021·2021-04-28
Smiths Medical Recalls LogiCal Monitoring Sets Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of LogiCal Monitoring Sets and related components due to insufficient or incomplete welds.
Product
LogiCal Monitoring Set, Model Number DPS564898. for blood pressure monitoring and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1458-2021·2021-04-28
Biotronik ILIVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 779 ILIVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, VR-T DF4 ProMRI, REF 404626, UDI: 04035479142131 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1461-2021·2021-04-28
Biotronik ILIVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik Inc is recalling 1,547 ILIVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, DR-T DF-1 PROMRI, REF 404622, UDI: 04035479142094 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2021·2021-04-28
Smiths Medical Recalls Left Heart Kits Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of Left Heart Kits and related components due to insufficient or incomplete welds.
Product
Left Heart Kit, Model Number M20268. for blood pressure monitoring.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1457-2021·2021-04-28
Biotronik ILIVIA 7 ICDs Recalled for Premature Battery Depletion
Biotronik is recalling 914 ILIVIA 7 ICDs due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, VR-T DF-1 ProMRI, REF 404625, UDI: 04035479142124 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V302000·2021-04-28
2021 Hyundai Elantra seat back recliner frame welding defect
Hyundai is recalling certain 2021 Elantra vehicles because the driver and front passenger seat back recliners may have been improperly welded and could separate during a crash, increasing injury risk.
Product
HYUNDAI — HYUNDAI ELANTRA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21118·2021-04-28
UST Recalls LifeSeasons Iron Supplement Due to Child-Resistant Packaging Failure
UST Mfg. LLC. is recalling LifeSeasons Blood Nourish-R iron supplements because the bottles do not meet child-resistant packaging requirements, posing a poisoning risk to young children.
Product
LifeSeasons Blood Nourish-R Iron Supplement
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1450-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 386 ITREVIA 7 implantable defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ITREVIA 7, VR-T DX DF-1, REF 393037, UDI: 04035479129521 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1464-2021·2021-04-28
Biotronik ILIVIA NEO 7 DR-T DF-1 ProMRI Defibrillators Recalled for Battery Depletion
Biotronik is recalling 98 ILIVIA NEO 7 DR-T DF-1 ProMRI defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI, REF 429529, UDI: 04035479156749 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21117·2021-04-28
Sauder Woodworking Recalls Counter-Height Bar Stools Due to Fall Hazard
Sauder Woodworking is recalling about 3,100 counter-height bar stools because the legs can become unstable, posing a fall hazard. No injuries have been reported.
Product
Sauder and Aliesha-May Counter-height bar stools (two-piece sets)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1434-2021·2021-04-28
Siemens Sensis Systems Recalled for Windows Service Permission Vulnerability
Siemens Medical Solutions is recalling Sensis and Sensis Vibe Hemo systems due to Windows Service Permission configuration risks that could expose sensitive information or allow data manipulation.
Product
Sensis/ Sensis Vibe Hemo systems with VD12A software as follows: Dedicated SIS Server- 6648153 Sensis Post-Processing Workstation- 6648161 Sensis- 10764561 VM Virtual Server- 10765502 Sensis High-End Servers- 10910620 Sensis Vibe Hemo- 11007641 Sensis Vibe Combo…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1435-2021·2021-04-28
Siemens BCS XP System Recalled for Potential Emicizumab Carryover
Siemens Healthcare Diagnostics is recalling BCS XP Systems due to a potential risk of Emicizumab carryover on patient samples.
Product
BCS XP System: Multipurpose system for in vitro coagulation studies. Product code: 10459330, 10461894, 10470625 - Product Usage: The Behring Coagulation System is an instrument intended to perform quantitative assays of a specific parameters in plasma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1465-2021·2021-04-28
Biotronik Intica Neo 7 HF-T Defibrillators Recalled for Battery Depletion
Biotronik is recalling eight Intica Neo 7 HF-T implantable defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI, REF 429553, UDI: 04035479156831 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1466-2021·2021-04-28
AngioDynamics Recalls Implantable Infusion Port Kits Due to Sterility Concerns
AngioDynamics is recalling specific lots of Smart Port CT-Implantable Port kits due to potential compromised sterility. The recall affects 267 kits distributed nationwide.
Product
Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient requiring repeated access of the vascular system, for delivery of medications, nutritional supplementation, fluids, blood, blood products, and sampling of blood and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1482-2021·2021-04-28
Welch Allyn ELI 280 Electrocardiograph Recalled for Safety Standard Non-Compliance
Welch Allyn is recalling 99 ELI 280 Electrocardiographs because they do not meet IEC 60601-2-27 safety requirements as labeled.
Product
ELI 280 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated for use on adult and pediatric populations.
Category
Medical Device
Distribution
Distributed nationwide