State

North Dakota product recalls

72,984 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total: 2,921
Critical: 265
Severe: 727
Most recent: 2026-09-02

Of the 2,921 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 727 (25%) are Severe.

Which agencies issued them

These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6601–6625 of 75905

SevereFDA (Devices)·Z-1750-2025·2025-05-21
TufTex Over-the-Wire Embolectomy Catheter incomplete sterile barrier
LeMaitre Vascular is recalling TufTex Over-the-Wire Embolectomy Catheters due to incomplete seals on some packages that compromise the sterile barrier. Affected units were distributed nationwide and internationally.
Product
TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1651-68, 1651-78, 1651-84, 1651-88, E1651-34, E1651-38, E1651-44, E1651-48, E1651-64, E1651-68, E1651-78, E1651-84, E1651-88, 1651-44J, 1651-48J, 1651-84J, 1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1698-2025·2025-05-21
AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.
Product
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1763-2025·2025-05-21
LifeShield Infusion Safety Software Recalled for Drug Library Defects
ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.
Product
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1727-2025·2025-05-21
iGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk
Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.
Product
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2025·2025-05-21
Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Product
Intera 1.5T R11, Model Number: 781170;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V330000·2025-05-21
Ram ProMaster rearview camera image may not display in reverse
Chrysler is recalling certain 2022-2025 Ram ProMaster vehicles because a software error in the security gateway module may prevent the rearview camera image displaying, failing FMVSS 111.
Product
RAM — RAM, BRAUN PROMASTER, RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E036000·2025-05-21
Holley Recalls Fuel Pressure Regulators Due to Leak Risk
Holley Performance Products is recalling specific Fuel Pressure Regulators because a damaged diaphragm may cause a fuel leak, increasing the risk of fire.
Product
FUEL SYSTEM, GASOLINE recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V334000·2025-05-21
Volkswagen Atlas rearview camera image can become distorted in reverse
Volkswagen is recalling certain 2024-2025 Atlas and Atlas Cross Sport vehicles because a software error may distort the rearview camera image when the vehicle is in reverse.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1783-2025·2025-05-21
Philips SmartPath to dStream 3.0T MRI Coil Adhesive Failure Recall
Philips is recalling SmartPath to dStream 3.0T MRI systems (Model 782145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
SmartPath to dStream for 3.0T, Model Number: 782145;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1782-2025·2025-05-21
Philips SmartPath dStream 1.5T MRI coil may create sharp edges
Philips is recalling SmartPath to dStream 1.5T MRI units (Model 782146) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, lacerations, or tissue injury to patients.
Product
SmartPath to dStream for 1.5T, Model Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1774-2025·2025-05-21
Philips Intera 1.5T MRI Quadrature Body Coil seal adhesive failure
Philips is recalling Intera 1.5T MRI systems due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and contact patient skin during scanning.
Product
Intera 1.5T, Model Numbers: 781195 and 781295;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2025·2025-05-21
Philips Intera 0.5T Standard MRI System Quadrature Body Coil Seal
Philips is recalling the Intera 0.5T Standard MRI system (Model 781101) because the Quadrature Body Coil seal adhesive may fail and create sharp edges that could injure patients during scanning.
Product
Intera 0.5T Standard, Model Number: 781101;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1770-2025·2025-05-21
Philips Enterprise 1.5T MRI Equipment Quadrature Body Coil Seal
Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Enterprise 1.5T, Model Number: 781145;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2025·2025-05-21
Halyard RAPIDES E-PACK Cardiovascular Procedure Kit Surgical Needle Coating Issue
AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Convenience Kits due to a raw material defect in surgical needle coating that may cause diminished performance or coating removal during use.
Product
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1748-2025·2025-05-21
Abbott Alinity m Resp-4-Plex Amplification Kit Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex Amplification Kit due to reports of reactive negative controls and false positive results in respiratory virus testing.
Product
Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the qualitative detection and differentiation of RNA from influenza A virus (flu A), influenza B virus (fl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2025·2025-05-21
KliniTray surgical alignment system recalled for microbial contamination risk
Klinika Medical is recalling the KliniTray tissue resection margin examination board (Model 2001105-F) due to potential microbial contamination. The device was distributed nationwide in Massachusetts.
Product
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and posi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1769-2025·2025-05-21
KliniTray Platte Faxitron Sterile Tissue Resection Examination Board Recalled
KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.
Product
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2025·2025-05-21
Pruitt Irrigation Occlusion Catheter Recalled for Incomplete Sterile Seals
LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.
Product
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V333000·2025-05-21
Mack Recalls 2026 MD Trucks Due to Incorrect Seat Belt Routing
Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1749-2025·2025-05-21
Abbott Alinity m Resp-4-Plex AMP Kit Multiplex PCR Test Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit (List Number 09N79-096) due to reports of increased reactive negative controls and false positive results in respiratory viral testing.
Product
Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the simultaneous qualitative detection and differentiation of RNA from SARS-CoV-2, influenza A virus (flu A), influenza B virus
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2025·2025-05-21
Pruitt Occlusion Catheter Recalled Due to Incomplete Sterile Barrier Seals
LeMaitre Vascular is recalling Pruitt Occlusion Catheters (catalog numbers 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56) because some packages have incomplete sterile barrier seals, potentially compromising product sterility.
Product
Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1775-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T Explorer/Nova Dual MRI scanners (Model 781108) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges that could contact patients during scanning and cause skin injuries.
Product
Intera 1.5T Explorer/Nova Dual, Model Number: 781108;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1776-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Body Coil Seal Failure Recall
Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.
Product
Intera 1.5T Master/Nova, Model Number: 781106;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2025·2025-05-21
Philips Intera 1.5T MRI Scanner QBC Seal Adhesive Failure Risk
Philips is recalling the Intera 1.5T Power/Pulsar MRI scanner because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 1.5T Power/Pulsar, Model Number: 781105;
Category
Medical Device
Distribution
Distributed nationwide