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.

26051–26075 of 76501

ModerateFDA (Devices)·Z-1580-2021·2021-05-19
ICU Medical Recalls Smallbore Trifuse Extension Sets Due to Leakage Defect
ICU Medical is recalling specific lots of Smallbore Trifuse Extension Sets because a molding defect may cause leakage in the inactivated position.
Product
REF CH3625 5" (13 cm) Appx 0.50 ml, Smallbore Trifuse Ext Set w/3 ChemoClave (Purple, Green Rings), Spiros w/Red Cap, 3 Clamps - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1578-2021·2021-05-19
ICU Medical Recalls Sprios Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of Sprios administration sets due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH3011 30" (76 cm) Appx 3.3 mL, 20 Drop Admin Set w/Integrated ChemoClave Drip Chamber, Spiros w/Red Cap, Bag Hanger - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1572-2021·2021-05-19
ICU Medical Recalls Oncology Kits Due to Molding Defect
ICU Medical is recalling specific lots of REF CL3538 Oncology Kits because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF CL3538 Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port, Vented Cap; ChemoLock , Spinning Spiros w/Red Cap - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1565-2021·2021-05-19
ICU Medical Recalls Oncology Kits Due to Molding Defect and Leakage
ICU Medical is recalling specific lots of Oncology Kits due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH3397 Oncology Kit w/Spiros¿, Red Cap, Bag Spike w/Clave Additive Port LOT 5118610 - Product Usage: for use in the preparation and patient administration of cytotoxic medications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1586-2021·2021-05-19
ICU Medical Recalls Spinning Spiros Male Luers Due to Molding Defect
ICU Medical is recalling specific lots of Spinning Spiros male luers because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF 20130-01 Spinning Spiros¿ Closed Male Luer, Red Cap REF CH2000S-PC Spinning Spiros¿ Closed Male Luer, Purple Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1590-2021·2021-05-19
ICU Medical Recalls Spinning Spiros Male Luers Due to Leakage Defect
ICU Medical is recalling specific lots of Spinning Spiros Closed Male Luers because a molding defect may cause leakage in the inactivated position.
Product
REF K7040-001 Spinning Spiros Closed Male Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1536-2021·2021-05-19
Fresenius AquaBplus Water Purification System Recalled for Installation Error
Fresenius Medical Care is recalling 27 AquaBplus water purification systems because an installation guideline error may reduce the effectiveness of heat disinfection.
Product
AquaBplus and AquaBplus B2 Water Purification System - Product Usage: Intended for use with a hemodialysis system to remove organic and inorganic substances and microbial contaminants from the water used for hemodialysis or related therapies. Fresenius P/N 24-2500-0 All 3…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1560-2021·2021-05-19
Haag-Streit LENSTAR LS900 Software Recall for Data Mixing Errors
Haag-Streit USA Inc is recalling Eyesuite 9.3.1 software for LENSTAR LS900 devices due to potential mixing of patient names and examination data.
Product
Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1587-2021·2021-05-19
ICU Medical Recalls Bag Spike Adapters Due to Molding Defect
ICU Medical is recalling specific lots of Bag Spike Adapters due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH3034 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap, Vented Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1575-2021·2021-05-19
ICU Medical Recalls Smallbore Extension Sets Due to Molding Defect
ICU Medical is recalling specific lots of smallbore extension sets because a molding defect may cause leakage in the inactivated position.
Product
REF CL4151 45" (114 cm) Appx 1.7 ml, Smallbore Ext Set w/Spiros w/Red Cap, Anti-Siphon Valve, Clamp, Y-Connector w/ChemoLock Port, Rotating Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1561-2021·2021-05-19
Remel Bile Esculin Azide Agar Recalled for Growth of E. faecalis
Remel Inc is recalling Bile Esculin Azide Agar with Vancomycin because the media allows growth of E. faecalis ATCC 29212.
Product
Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative procedures as a screening method for primary isolation and presumptive identification of vancomycin-resistance enterococci (VRE) from surveillance cultures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1589-2021·2021-05-19
ICU Medical Recalls IV Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of IV administration sets because a molding defect may cause leakage in the inactivated position.
Product
REF CH3762 35" (89 cm) Appx 3.9 ml, 10 Drop Admin Set w/Integrated Clave" Drip Chamber, Clave", Spiros" w/Red Cap, Bag Hanger - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1562-2021·2021-05-19
Musculoskeletal Transplant Foundation Recalls AFT Straight Tubes Due to Filling Error
Musculoskeletal Transplant Foundation is recalling AFT Straight Tubes that were filled only halfway instead of three-quarters, which may cause surgery delays.
Product
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1574-2021·2021-05-19
ICU Medical Recalls Oncology Kits Due to Potential Leakage Defect
ICU Medical is recalling specific lots of Oncology Kits because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF CL3960 Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros ; w/ChemoLock; Syringe Transfer Set w/MicroClave, w/ChemoLock Port - Product Usage: provides access for the administration of fluids from a container to a…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V364000·2021-05-18
MCI Recalls Diesel Buses Due to Fuel Rail Leak Fire Risk
Motor Coach Industries is recalling specific 2017-2021 MCI diesel buses because a fuel rail leak could cause a fire.
Product
MCI — MCI D4000ISTV, J3500, D4000, D4005
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V365000·2021-05-18
New Flyer Recalls Buses Due to Fuel Rail Leak Fire Risk
New Flyer is recalling certain 2016-2021 XD and XDE series buses because a fuel rail leak could cause a fire.
Product
NEW FLYER — NEW FLYER XD35, XD60, XD40, XDE60
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·018-2021·2021-05-17
Kraft Heinz Recalls Chef Francisco Soup Due to Undeclared Allergens
Kraft Heinz is recalling Chef Francisco soup products because they contain undeclared milk and eggs. The mislabeled frozen soup was distributed to foodservice establishments nationwide.
Product
Kraft Heinz Foods Company — Kraft Heinz Foods Company Recalls Chef Francisco Soup Product Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·21V359000·2021-05-17
Mercedes-Benz Recalls 2020 Sprinter Vans for Door Hinge Screw Issue
Daimler Vans USA is recalling 2020 Mercedes-Benz Sprinter vans because front door hinge screws may not be tightened properly, increasing injury risk in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 2500, SPRINTER 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V363000·2021-05-17
Husqvarna 701 Enduro LR Recalled for Fuel Line Chafe Risk
KTM is recalling 2020 Husqvarna 701 Enduro LR motorcycles because fuel lines may chafe and leak, increasing fire risk.
Product
HUSQVARNA — HUSQVARNA 701 ENDURO LR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V361000·2021-05-17
2021 Ducati Scrambler Turn Signals May Not Flash Brightly Enough
Ducati is recalling certain 2021 Scrambler 800 Night Shift motorcycles because the front and rear turn signal lights may not flash brightly enough, reducing visibility to other drivers and increasing crash risk.
Product
DUCATI — DUCATI SCRAMBLER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V360000·2021-05-17
Mercedes-Benz Recalls 2019 Sprinter Vans for Stability Control Software Update
Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vans with camper upfits because the Electronic Stability Control software was not updated for their higher center of gravity.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER (VS30)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V362000·2021-05-17
2021 Porsche Taycan and Panamera Front Suspension Trailing Arm Defect Recall
Porsche is recalling certain 2021 Taycan and Panamera models due to front lower trailing arms that may not be properly forged and could break, risking loss of vehicle control.
Product
PORSCHE — PORSCHE PANAMERA 4S E-HYBRID, PANAMERA 4S, PANAMERA 4 E-HYBRID, PANAMERA TURBO S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V358000·2021-05-17
Sutphen Recalls One 2012 SP70 Vehicle for Display Lockup Issue
Sutphen is recalling one 2012 SP70 vehicle because low voltage spikes may cause the LCD display to lock up, potentially delaying emergency efforts.
Product
SUTPHEN — SUTPHEN SP70
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V352000·2021-05-14
Gillig Recalls 2017-2020 Low Floor Vehicles Due to Fuel Leak Risk
Gillig is recalling 2017-2020 Low Floor vehicles because a fuel rail leak could cause a fire. Owners should contact Gillig for a free inspection and repair.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V353000·2021-05-14
Mercedes-Benz 2019-2021 G63 and G550 Rear Door Latch Defect
Mercedes-Benz is recalling 2019-2021 G550 and G63 AMG vehicles for defective rear door latches that may not engage properly or open while driving, creating risk of injury or crashes. Dealers will replace the latches free of charge.
Product
MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63
Category
Vehicle
Distribution
Distributed nationwide