State

North Dakota product recalls

72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5951–5975 of 75892

HighFDA (Food)·H-0294-2025·2025-07-23
YoCrunch vanilla yogurt with M&M toppers may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, Packaged in the following size containers: 1. Single Serve Cup 6 oz (170g) UPC 46675-00079 2. Multipack consisting of 4-4 oz. cups UPC 46675-01351 Keep Refrigerated. Distributed by Danone US, White Plai
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2120-2025·2025-07-23
VITROS Performance Verifier I lots can cause quality control drift
VITROS Chemistry Products Performance Verifier I is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier I Model/Catalog Number: 806 7324 Software Version: Not Applicable Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor perfo
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2119-2025·2025-07-23
NIO+ intraosseous device stabilizer may not release properly after insertion
The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.
Product
Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intraosseous access device supplied Sterile and single use. Indicated for Intraosseous access to t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0521-2025·2025-07-23
Levothyroxine sodium 100 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 100 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 9,739 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2111-2025·2025-07-23
BLS DIODE laser projectors shipped without a working remote interlock connector
BLS laser light show projectors, models DIODE 1000, 2000 and 3000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 10 units affected.
Product
Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.
Category
Other
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0520-2025·2025-07-23
Levothyroxine sodium 50 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2118-2025·2025-07-23
NIO-A intraosseous device stabilizer may not release properly after insertion
The NIO-A NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 7,056 US units affected.
Product
Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2025·2025-07-23
VITROS CHE slides can cause quality control drift with performance verifiers
VITROS Chemistry Products CHE Slides are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
Product
VITROS Chemistry Products CHE Slides; Catalog Numbers: (1) 191 4605 (300 slides), (2) 800 4707 (90 slides);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0549-2025·2025-07-23
Power Stick Spring Fresh roll-on antiperspirant recalled over manufacturing deviations
Beauty & Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant Spring Fresh is being recalled because of CGMP deviations. 22,482 cases are affected.
Product
Beauty & Skincare Power Stick original nourishing invisible protection roll-on Antiperspirant/Deodorant Spring Fresh, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-039-00, UPC Code 815195018194
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0516-2025·2025-07-23
Lisdexamfetamine 60 mg capsules failed dissolution testing at nine month stability
Lisdexamfetamine Dimesylate Capsules 60 mg are being recalled because an out of specification result was observed in dissolution testing at the nine month long term stability station. 5,448 bottles affected.
Product
LISDEXAMFETAMINE DIMESYLATE — LISDEXAMFETAMINE DIMESYLATE (LISDEXAMFETAMINE DIMESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0548-2025·2025-07-23
Power Stick for her roll-on antiperspirant recalled over manufacturing deviations
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent is being recalled because of CGMP deviations. 21,265 cases are affected.
Product
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0550-2025·2025-07-23
Power Stick roll-on antiperspirant recalled over manufacturing practice deviations
Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant is being recalled because of CGMP deviations. 23,467 cases are affected.
Product
Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz./ 53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-040-00 UPC Code 815195018224
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2114-2025·2025-07-23
NeuroSync EYE-SYNC headsets are inoperable and cannot be repaired
NeuroSync EYE-SYNC systems containing Pico Neo 2 headsets are being recalled because eye syncing issues render the device inoperable and it cannot be repaired. 27 units are affected.
Product
NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists of a Pico Neo 2 headset with embedded sensors, a paired Android tablet, and proprietary software, packaged in a portable field case. Eye-tracking headset system is intended for recording, viewing, and analyz
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0273-2025·2025-07-23
New Mexico Pinon single serve coffee cup ink can run
New Mexico Pinon Coffee Dark Pinon Single Serve cups are being recalled because an inconsistent clear coat seal allows the food safe ink printing to run in a K-cup machine. 154 units affected.
Product
New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Number:F03308 UPC:812361033081. Single Serve (Keurig) Cups, filled with ground coffee flavored with natural flavorings.
Category
Food
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0517-2025·2025-07-23
Compounded testosterone pellet vials carry incorrect lot numbers from printing issue
Compounded Testosterone 200 mg Pellet in 1 mL amber vials is being recalled because a printing issue resulted in incorrect lot numbers on the label. 2,832 vials are affected.
Product
Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only, Compounded product. Qualgen 14844 Bristol Park Blvd Edmond OK 73013, NDC 69761-202-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V476000·2025-07-22
Nova Bus steering can turn without driver input from missing valve
Nova Bus is recalling certain 2020-2023 LFS transit buses because the electric power steering system may be missing a check valve, allowing hydraulic pressure to turn the steering wheel on its own.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V478000·2025-07-22
Winnebago airbag wiring can be caught in the seat mechanism
Winnebago is recalling certain 2024-2026 motorhomes because Supplemental Restraint System wires can be caught in the seat mechanism when the front seats are adjusted, damaging them.
Product
WINNEBAGO — WINNEBAGO REVEL, EKKO, NAVION, VIEW
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V477000·2025-07-22
Lamborghini Recalls 2024-2025 Revuelto Vehicles for Door Spring Defect
Lamborghini is recalling 2024-2025 Revuelto vehicles because gas springs may fail, causing doors to close unexpectedly and increasing injury risk.
Product
LAMBORGHINI — LAMBORGHINI REVUELTO
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·25393·2025-07-21
Above-ground pools recalled after nine children drowned using strap footholds
Above-ground pools 48 inches and taller with compression straps over the vertical support legs are being recalled because the strap can create a foothold. CPSC believes nine children have drowned.
Product
48-inch and taller above-ground pools with compression straps running on the outside and over the vertical support legs
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V475000·2025-07-21
Rosenbauer Fire Trucks Recalled for Odometer Software Error
Rosenbauer America is recalling 2019-2024 fire trucks because a software error may cause the odometer to freeze, potentially delaying critical safety maintenance.
Product
ROSENBAUER — ROSENBAUER WARRIOR, COMMANDER, AVENGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V473000·2025-07-17
Grand Design trailer entrance door latch mechanism may fail
Grand Design is recalling certain 2025-2026 Lineage trailers with Lippert Modularia entrance doors because the door latch mechanism may fail, potentially trapping occupants in an emergency.
Product
GRAND DESIGN — GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·026-2025·2025-07-17
Kayem Foods Recalls Chicken Sausage Due to Plastic Contamination
Kayem Foods is recalling ready-to-eat chicken sausage products nationwide due to possible contamination with pieces of plastic.
Product
Kayem Foods Inc. — Kayem Foods Inc. Recalls Ready-To-Eat Chicken Sausage Products Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereCPSC·25390·2025-07-17
iStore magnetic wireless power banks can overheat and ignite while charging
iStore Magnetic Wireless Power Banks, model IST-09991/W05, are being recalled because the lithium-ion battery can overheat and ignite while charging. Three incidents and about $15,000 in property damage reported.
Product
iStore Magnetic Wireless Power Banks (IST-09991/W05 model only)
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25389·2025-07-17
CasaClean handheld steamers can leak steam or spew hot boiling water
CasaClean Handheld Steamers, model DF-958, are being recalled because they can leak steam or spew hot boiling water. Thirteen consumers have received burns. About 23,000 units are affected.
Product
CasaClean Handheld Steamers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25387·2025-07-17
Traveller aluminum loading ramps can bend or break under rated loads
Traveller aluminum loading ramps are being recalled because they cannot withstand the weight specified on the ramps and can bend or break in use. Two injuries have been reported. About 18,000 units affected.
Product
Traveller Aluminum Loading Ramps
Category
Consumer Product
Distribution
Distributed nationwide