The Recall Desk

State

North Dakota product recalls

72,968 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.

These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5251–5275 of 75889

  • ModerateFDA (Devices)·Z-2579-2025·2025-09-24

    Fourteen millimetre distraction pins recalled over unvalidated shelf life labeling

    Frontier Devices 14 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 10,960 units are affected.

    Product
    Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 10 single packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0647-2025·2025-09-24

    Chlorpromazine 25 mg blisterpacks recalled over micro-organism on packaging coil

    Chlorpromazine Hydrochloride Tablets, USP, 25 mg, in blisterpacks from American Health Packaging, are recalled because a micro-organism was found on a lot of packaging coil. 2,708 cartons are affected.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0587-2025·2025-09-24

    Adderex XR focus tablets recalled over unapproved drug claims and misbranding

    Hi-Tech Pharmaceuticals Adderex XR, 30 tablets, lot 303120691, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS ADDEREX XR STRONGEST FOCUSING AID WITHOUT A PRESECRIPTION! HELPS ADULTS MAINTAIN CONCENTRATION & IMPROVE PRODUCTIVITY! 30 TABLETS UPC 8 11836 02691 7 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0593-2025·2025-09-24

    Slimaglutide weight loss supplement recalled over unapproved drug claims and misbranding

    Hi-Tech Pharmaceuticals Slimaglutide, 180 tablets, lot C19El8, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST AND SECRETAGOGUES NOVEL GIP (GLUCOSE-DEPENDENT ISNULINOTROPIC POLYPEPTIDE) RECEPTOR AGONIST 180 TABLETS DIETARY SUPPLEMENT
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0590-2025·2025-09-24

    Joint supplement recalled over unapproved drug claims on the label

    Hi-Tech Pharmaceuticals Joint-RX dietary supplement, 90 count, lot 503110607, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity Dr Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2582-2025·2025-09-24

    Blood gas cartridges recalled for lacking clearance covering updated measurement ranges

    i-STAT CG4+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting the updated lactate sample type and pH and PO2 measurement ranges. 9,067,050 units are affected.

    Product
    i-STAT CG4+ cartridge (white). List Number: 03P85-25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2583-2025·2025-09-24

    Blood gas CG8+ cartridges recalled for lacking updated premarket clearance

    i-STAT CG8+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 8,962,450 units are affected.

    Product
    i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0599-2025·2025-09-24

    Uric acid control capsules recalled over unapproved drug claims on label

    Top Secret Nutrition Extra Strength Uric Control, 30 veggie caps, lot C1238, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.

    Product
    Top Secret Nutrition extra strength uric control fast acting multi-pronged uric acid control 30 veggie caps DIETARY SUPPLEMENT UPC 8 11226 02158 4 Distributed by: TOP SECRET NUTRITION, LLC 6015-B Unity Dr. Norcross, GA 30052
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2578-2025·2025-09-24

    Distraction pins in five packs recalled over unvalidated shelf life

    Frontier Devices 14 mm Distraction Pins in 5 single packs are recalled because the labeling includes a shelf life that has not been validated. 2,700 units are affected.

    Product
    Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 5 single packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0586-2025·2025-09-24

    Flexible joint formula capsules recalled over unapproved drug claims on label

    Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis, 240 capsules, lot 405310805, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.

    Product
    FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH CARTILAGE LUBRICATES JOINTS 240 Capsules UPC 7 97573 90884 1 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2585-2025·2025-09-24

    Blood gas EG6+ cartridges recalled for lacking updated premarket clearance

    i-STAT EG6+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 547,250 units are affected.

    Product
    i-STAT EG6+ cartridge. List Number: 03P77-25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2560-2025·2025-09-24

    Lactate slides in 18-slide cartridges recalled over calibration failures delaying results

    VITROS Chemistry Products LAC Slides, catalog 8150112, from coating 0130 and above are recalled because of increased calibration failures on VITROS XT systems, delaying lactate results. 2,320 units are affected.

    Product
    VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slides, for a total of 90 tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0596-2025·2025-09-24

    Battle Hardener supplement cycle recalled over unapproved drug claims

    LG Sciences Battle Hardener Platinum Series complete 6 week cycle with PCT is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.

    Product
    LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH PCT LEGAL GEAR DIETARY SUPPLEMENT 17-PROANDRO pBOLD FORM-XT UPC 7 44890 94151 6 MADE FOR LG SCIENCES 6015-B UNITY DR. NORCROXX, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Drugs)·D-0650-2025·2025-09-24

    Packaged chlorpromazine cartons recalled over micro-organism on packaging coil

    Chlorpromazine Hydrochloride Tablets, USP, 200 mg, in blister cartons from American Health Packaging, are recalled because a micro-organism was found on a lot of packaging coil. 873 cartons are affected.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V635000·2025-09-23

    Blue Bird Recalls Vision Buses Due to Brake Software Defect

    Blue Bird is recalling 2021-2026 Vision school and transit buses because brake software may activate the parking brake unexpectedly, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V634000·2025-09-23

    Porsche Cayenne, Panamera fuel pump fasteners inadequately tightened

    Porsche is recalling certain 2024–2026 Cayenne and Panamera models because fasteners securing the high pressure fuel pump may not be tightened properly, creating a fuel leak risk and potential fire hazard.

    Product
    PORSCHE — PORSCHE PANAMERA, CAYENNE, PANAMERA 4 E-HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V636000·2025-09-23

    BMW and Toyota Supra starter relays can corrode and short circuit

    BMW is recalling certain 2019-2022 BMW models and the Toyota Supra because the engine starter relay may corrode, overheat and short circuit. Owners are told to park outside until repaired.

    Product
    BMW — BMW, TOYOTA 230I, 530I, SUPRA, Z4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V628000·2025-09-19

    Ford Recalls 2020 Expedition and Lincoln Navigator for Fire Risk

    Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a short circuit in the battery junction box can cause an engine fire.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V630000·2025-09-19

    Isuzu and Chevrolet truck fuel heaters can overheat and leak fuel

    Isuzu is recalling certain 2022-2026 FVR, FTR and Chevrolet 6500XD and 7500XD vehicles because the fuel heater may overheat, melting the casing and allowing fuel to leak into the electrical connector.

    Product
    CHEVROLET — CHEVROLET, ISUZU 7500XD, 6500XD, FVR, FTR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V626000·2025-09-19

    Ford Super Duty steering column upper shaft can detach

    Ford is recalling certain 2020-2021 F-250, F-350 and F-450 vehicles because the steering column upper shaft may detach from the steering column, causing a loss of steering control.

    Product
    FORD — FORD F-350 SD, F-250 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V631000·2025-09-19

    New Flyer Recalls Transit Buses Due to High Voltage Battery Fire Risk

    New Flyer is recalling 2019-2025 XE35, XE40, and XE60 transit buses because a high voltage battery short circuit may cause a fire. Owners should park outside and limit charging to 75%.

    Product
    NEW FLYER — NEW FLYER XE35, XE40, XE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V632000·2025-09-19

    MCI Recalls 2024-2025 Electric Coaches Due to Battery Fire Risk

    Motor Coach Industries is recalling specific 2024 and 2025 electric coaches because a high-voltage battery short circuit could cause a fire.

    Product
    MCI — MCI D45CRTELE, J4500E, D45CRTE
    Category
    Vehicle
    Distribution
    Distributed nationwide