State

North Dakota product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8451–8475 of 75913

HighFDA (Devices)·Z-0676-2025·2024-12-18
Philips Allura Xper X-ray Systems Prone to Clamping Bolt Failure and Collision Risk
Philips Allura Xper radiological systems may experience propeller motor and x-ray tube locking bolt breaks, causing erratic C-arm movements with potential for collision with patients or bystanders, and unnecessary radiation exposure.
Product
Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Number: 722010. 2. Allura Xper FD10/10, Model Number: 722011. 3. Allura Xper FD20, Model Number: 722012. 4. Allura Xper FD20 Biplane, Model Number: 722013. 5. Allura Xper
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0674-2025·2024-12-18
Convertor Isolation Gowns may fail protective barrier requirements
Cardinal Health is recalling 940,203 Convertor Isolation Gowns because raw materials may prevent them from meeting AAMI Level 3 protection specifications.
Product
Convertor Isolation Gown, AAMI Level 3 protection, Product Codes AT6100, AT6100-XL, AT6200, and AT6200-XL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0670-2025·2024-12-18
BD Pyxis MedStation ES Automated Medication Cabinet Recalled for Software Defect
An automated medication dispensing cabinet may open the wrong storage pocket due to a software malfunction, potentially leading to incorrect medication removal. The manufacturer is recalling affected units.
Product
BD Pyxis MedStation ES, REF: 323
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V937000·2024-12-18
2025 Chevrolet Silverado EV Pedestrian Alert System Sound Volume
General Motors is recalling certain 2025 Chevrolet Silverado EV work trucks because the pedestrian alert sound system may not produce sound at sufficient volume. This increases the risk of pedestrians being unaware of an approaching vehicle.
Product
CHEVROLET — CHEVROLET SILVERADO EV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0679-2025·2024-12-18
Galaxy Bronchoscope Biopsy Tool Insertion Risk at Sharp Bend Angles
Noah Medical is recalling Galaxy bronchoscope units due to risk that biopsy tools may require excessive force or fail to pass through the scope channel when the bronchoscope is sharply bent, potentially causing tissue injury or pneumothorax.
Product
Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0269-2025·2024-12-18
Cucumber Chunk & Tomato Wedge Recalled for Salmonella Risk
Sysco Corporation is recalling Cucumber Chunk & Tomato Wedge products due to potential Salmonella contamination in cucumbers. Products were distributed in Iowa, Minnesota, South Dakota, North Dakota, Wisconsin, and Canada.
Product
Cucumber Chunk & Tomato Wedge Item 11835. 2/2.5 lb. Keep Refrigerated
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0665-2025·2024-12-18
MICRO-X Rover Mobile X-ray System delivers lower-than-set radiation doses
Micro-X Ltd. is recalling 18 MICRO-X Rover Mobile X-ray Systems because they can deliver lower radiation doses than operators set. The affected units use Control Board PCBA 12425-03 or earlier.
Product
MICRO-X Rover Mobile X-ray System, # MXU-RV35; MICRO-X Rover Mobile X-ray System, # MXU-RV71
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0118-2025·2024-12-18
Drug Recall: Levothyroxine Sodium Tablets Affected by Potency Failures
Viatris Inc recalls 92,512 bottles of Levothyroxine Sodium tablets with potency failures—some are stronger than intended, others are weaker than intended.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0262-2025·2024-12-18
Dietary supplement recalled for undeclared soy lecithin allergen
DesBio lunaSOMM Natural Sleep Support Dietary Supplement is recalled due to undeclared soy lecithin. The product is labeled as containing sunflower lecithin but contains soy lecithin, posing a risk to consumers with soy allergies.
Product
DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap. Supplement facts declare Phosphatidylserine (from non-GMO sunflower lecithin powder) 40 mg. Distributed by Deseret Biologicals Inc 469 West Parkland Dr, Sandy, UT.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0671-2025·2024-12-18
Automated Dispensing Cabinet Software Flaw May Cause Medication Dispensing Errors
The BD Pyxis MedStation ES automated dispensing cabinet may dispense the wrong medication due to a software issue, potentially causing medication errors and inventory shortages.
Product
BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V938000·2024-12-18
Volvo Recalls 2023-2024 C40 Vehicles for Air Bag Clamp Defect
Volvo is recalling 2023-2024 C40 vehicles because improperly crimped clamps may cause the driver's air bag to deploy improperly, increasing injury risk.
Product
VOLVO — VOLVO C40BEV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0675-2025·2024-12-18
Cardinal Health isolation gowns recalled for failing hydrostatic pressure standards
Cardinal Health is recalling 940,203 SMS Elastic Cuff Thumbhook Level 3 Isolation Gowns because the raw materials may fail hydrostatic pressure specifications, preventing them from meeting required AAMI Level 3 protection standards.
Product
Cardinal Health SMS Elastic Cuff Thumbhook Level 3 Isolation Gown, Full-Back, Product Codes AT6588-2XL, AT6588-BD, AT6588-XL, AT6688-2XL, AT6688-BD, and AT6688-XL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0122-2025·2024-12-18
Levothyroxine Sodium Tablets Recalled Due to Potency Failures
Viatris Inc. is recalling Levothyroxine Sodium 200 mcg tablets nationwide due to potency failures—some tablets are superpotent while others are subpotent. Affected lots expire July 2025; patients should contact their healthcare provider.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0135-2025·2024-12-18
FDA Recalls Levothyroxine Sodium Tablets for Potency Variation
Mylan Institutional recalls 690 cartons of Levothyroxine Sodium 150 mcg tablets nationwide due to potency variation. Some units may be subpotent or superpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0664-2025·2024-12-18
MICRO-X Rover Mobile X-ray System Exposure Timing Defect Recalled
Micro-X Ltd. is recalling five MICRO-X Rover Mobile X-ray Systems due to a timing defect that prevents adequate X-ray exposures. The 4 millisecond exposure time does not allow sufficient tolerance for diagnostic-quality imaging.
Product
MICRO-X Rover Mobile X-ray System, # MXU-RV35
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0120-2025·2024-12-18
Levothyroxine sodium tablets recalled for potency failures nationwide
Viatris Inc is recalling Levothyroxine Sodium Tablets USP 150 mcg nationwide due to potency failures. Affected lots containing both subpotent and superpotent tablets expire June 2025.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0127-2025·2024-12-18
Levothyroxine sodium tablets recalled for potency failures nationwide
Viatris Inc is recalling Levothyroxine Sodium 100 mcg tablets for potency failures causing some tablets to be too strong and others too weak. Approximately 65,169 units are affected nationwide.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0124-2025·2024-12-18
Levothyroxine Sodium Tablets Recalled for Potency Variation and Dosage Failures
Viatris Inc. is recalling 42,331 bottles of Levothyroxine Sodium Tablets 50 mcg distributed nationwide due to potency failures resulting in both superpotent and subpotent tablets.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0136-2025·2024-12-18
Levothyroxine Sodium Tablets Recalled for Subpotent and Superpotent Content
Mylan Institutional is recalling Levothyroxine Sodium tablets nationwide due to subpotent and superpotent units. Patients taking affected tablets may receive incorrect doses of this thyroid medication.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0113-2025·2024-12-18
Varithena Administration Pack Recalled Due to Incorrect Syringe Connector Type
Biocompatibles is recalling 432 Varithena (polidocanol injectable foam) Administration Packs due to incorrect syringe connectors. The packs contain luer lock syringes instead of the required luer slip connection syringes.
Product
Varithena (polidocanol injectable foam) Administration Pack, Contains: 3 silicone-free syringes, 2 compression pads, 1 Varithena Transfer Unit, 1 manometer tubing, Rx Only, Distributed by Biocompatibles Inc., a BTG International Group company. CN01114.3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0117-2025·2024-12-18
FDA Recalls JAVYGTOR Tablets Due to Failed Impurities and Degradation Specifications
Dr. Reddy's Laboratories is recalling 7,233 bottles of JAVYGTOR (sapropterin dihydrochloride) tablets nationwide because the medication failed specifications for impurities and degradation products. Affected patients should contact their healthcare provider.
Product
JAVYGTOR — JAVYGTOR (SAPROPTERIN DIHYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0669-2025·2024-12-18
Hologic Sizer Set Missing Instructions for Use and Sterilization
Hologic is recalling 178 units of Sizer Set surgical instruments nationwide because instructions for use and revised sterilization instructions were not provided with the product.
Product
Hologic Sizer Set- sterilization tray and 6 individual sizers, intended as a Surgical instrument guide Model/Catalog Number: F0101
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0115-2025·2024-12-18
OTC Cold and Flu Medication Recalled Due to Manufacturing Process Deviations
LNK International recalls Kirkland Severe Cold & Flu Plus Congestion due to Current Good Manufacturing Practice (CGMP) deviations. The product should not have been released and was distributed to wholesale customers.
Product
SEVERE COLD AND FLU PLUS CONGESTION — SEVERE COLD AND FLU PLUS CONGESTION (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0652-2025·2024-12-18
ICU Medical ChemoLock Closed System Transfer Device Packaging Recall
ICU Medical is recalling 6,000 units of ChemoLock Close Vial Spike (Model CL-80) due to incorrect packaging and labeling of finished goods. Units were distributed in Illinois and Canada.
Product
ChemoLock Close Vial Spike REF CL-80 The Chemolock Closed System Transfer Device prevents the transfer of environmental contaminants. The Chemolock is needle free and cannot be deactivated, which will passively aid in preventing needlestick injuries and the exposure to cytoto
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V934000·2024-12-17
Cummins Recalls 2022-2024 Trailer-Mounted Generators Due to Wiring Defect
Cummins is recalling 2022-2024 C275D2RE trailer-mounted generators because unsecured wire leads may chafe and short circuit, increasing the risk of electrical shock or fire.
Product
CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
Category
Vehicle
Distribution
Distributed nationwide