The Recall Desk

State

North Dakota product recalls

73,218 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,924
Critical
265
Severe
729
Most recent
2026-09-23

Of the 2,924 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 729 (25%) are Severe.

Which agencies issued them

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15526–15550 of 76142

  • HighFDA (Drugs)·D-0931-2023·2023-07-26

    Norepinephrine injectable recalled due to sterility assurance concerns

    SterRx is recalling norepinephrine injections due to lack of assurance of sterility. The recall affects 132,299 bags distributed nationwide.

    Product
    Norepinephrine 4 mg per 250 mL (16 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-552-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0934-2023·2023-07-26

    Norepinephrine Injectable Recalled Due to Lack of Sterility Assurance

    SterRx recalled 2,088 bags of Norepinephrine 32 mg per 250 mL (Lot #490100) distributed nationwide due to lack of sterility assurance. The recall affects a critical care medication used in intensive care settings.

    Product
    Norepinephrine 32 mg per 250 mL (128 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-702-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0924-2023·2023-07-26

    Loteprednol Etabonate Eye Drops Recalled for Out-of-Specification Potency

    Sun Pharmaceutical recalls Loteprednol Etabonate eye drops due to out-of-specification unit dose content in certain lots. Affected bottles may contain incorrect potency levels.

    Product
    LOTEPREDNOL ETABONATE — LOTEPREDNOL ETABONATE (LOTEPREDNOL ETABONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0927-2023·2023-07-26

    FDA Recalls Phenylephrine HCl IV Solution Over Manufacturing Contamination

    Advanced Compounding Solutions is recalling 82 bags of phenylephrine HCl intravenous solution due to potential contamination from manufacturing facility violations. No illnesses have been reported.

    Product
    PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride 250mL, 250 mL IV Bag @60 Total volume), RX only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC: 71546-450-25;
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2146-2023·2023-07-26

    Aesculap Surgical Needle Recalled for Incorrect Product Code Marking

    Aesculap Implant Systems is recalling Aesculap Surgical Needles (MD610) because they are etched with an incorrect product code. The needles are marked MD611 when they should be marked MD610.

    Product
    Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0939-2023·2023-07-26

    Famotidine tablets recalled for carton labeling error on strength

    Glenmark Therapeutics is recalling famotidine 20 mg tablets after some cartons were labeled with a side label indicating 10 mg instead. The medication inside is correct; only the external carton label is mislabeled.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0925-2023·2023-07-26

    Prescription drug recall: Fingolimod capsules fail dissolution specifications

    Ascend Laboratories is recalling 2,652 bottles of Fingolimod capsules nationwide because they failed to meet dissolution specifications, potentially affecting medication effectiveness.

    Product
    FINGOLIMOD — FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23E057000·2023-07-25

    RevHD Recalls Oil Hubcaps Due to Fire and Crash Risk

    RevHD is recalling specific oil and PSI oil hubcaps because the lens may become loose, causing lubricant leaks that can overheat wheel bearings and increase the risk of fire or a crash.

    Product
    WHEELS:HUBCAP/COVER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V514000·2023-07-24

    Mack Recalls 2022-2023 LRBE Electric Trucks Due to Battery Fire Risk

    Mack Trucks is recalling 2022-2023 LRBE electric trucks because over-tightened battery inserts may break, causing a short circuit and increasing fire risk.

    Product
    MACK — MACK LRBE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V512000·2023-07-24

    Volvo Recalls 2020-2024 VNR Electric Trucks Due to Battery Fire Risk

    Volvo Trucks is recalling 2020-2024 VNR Electric vehicles because over-tightened battery inserts may break, causing a short circuit and increasing fire risk.

    Product
    VOLVO — VOLVO VNRE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E056000·2023-07-24

    Allison Transmission Recalls Emergency Vehicle Transmission Control Modules

    Allison Transmission is recalling 584 Emergency Vehicle Series 6th Generation Transmission Control Modules that may fail to engage 4th gear lockup, preventing the water pump from operating.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V511000·2023-07-24

    2022-2024 Volvo Trucks Windshield Wiper Motor Failure Recall

    Volvo Trucks is recalling 2022-2024 commercial trucks due to windshield wiper motor gears that may wear and fail, reducing visibility. Dealers will replace the motor assembly at no cost.

    Product
    VOLVO — VOLVO VNR, VAH, VNL, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V510000·2023-07-21

    2023 Ford F-53 and F-59 Recalled for Inoperative Instrument Panel

    Corrosion in the Smart Data Link Connector may prevent the instrument panel from displaying critical safety information like the speedometer and warning lights in certain 2023 Ford F-53 and F-59 vehicles, increasing crash risk.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V504000·2023-07-21

    Peterbilt and Kenworth trucks recalled for loose driveline fasteners

    PACCAR is recalling certain 2023-2024 Peterbilt and Kenworth trucks due to improperly applied thread-lock on driveline fasteners. Loose fasteners could allow the driveline to separate, increasing crash risk.

    Product
    KENWORTH — KENWORTH, PETERBILT T280, 536, 537, T480
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V507000·2023-07-21

    2023 Ford Super Duty Trucks Door Window Auto-Reverse May Fail

    Ford is recalling 2023 Super Duty F-250, F-350, F-450, and F-550 trucks due to a door module power issue that may prevent the power window anti-pinch function from detecting obstructions and automatically reversing.

    Product
    FORD — FORD F-550 SD, F-250 SD, F-450 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V503000·2023-07-21

    Forest River Recalls 2023 Impression Fifth Wheels Due to Fire Risk

    Forest River is recalling 2023 Impression fifth wheels because the exterior griddle may be stowed while connected to the LP gas line, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER IMPRESSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V506000·2023-07-21

    2023 Ford Super Duty Trucks and Escape Instrument Panel Illumination Defect

    Ford is recalling certain 2023 Super Duty F-250, F-350, F-450, F-550 and Escape models. The instrument panel module may fail to illuminate due to improper soldering, preventing drivers from seeing critical safety information like the speedometer and warning lights.

    Product
    FORD — FORD F-350 SD, ESCAPE, F-550 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V500000·2023-07-20

    2023 Chrysler Pacifica Plug-In Hybrid Fuel Line Defect Recall

    Certain 2023 Chrysler Pacifica Plug-In Hybrid Electric vehicles may have deformed fuel lines that could leak, increasing fire risk. Dealers will replace the fuel lines free of charge.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23774·2023-07-20

    CUPKIN Stainless Steel Children's Cups Recalled for Excessive Lead Content

    SOOJIMUS is recalling about 346,000 CUPKIN Double-Walled Stainless Steel Children's Cups because they contain lead levels that exceed the federal ban. Lead ingestion poses a health risk to young children.

    Product
    CUPKIN Double-Walled Stainless Steel Children's Cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23247·2023-07-20

    Wild Country Superlight Rocks climbing chocks recalled for fall hazard

    Salewa USA recalls Wild Country Superlight Rocks cable wire climbing chocks due to corrosion from seaside exposure that weakens and breaks the chocks, creating a fall hazard for climbers. No injuries have been reported in the U.S.

    Product
    Superlight Rocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23775·2023-07-20

    Pottery Barn Kids Penny Convertible Cribs Recalled for Laceration Hazard

    Williams-Sonoma Inc., operating as Pottery Barn Kids, is recalling about 310 Penny Convertible Cribs because the end panel can become loose and expose sharp edges, creating a laceration hazard to children. No injuries have been reported.

    Product
    Pottery Barn Kids Penny Convertible Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1236-2023·2023-07-19

    FDA Recalls Rader Farms Organic Fresh Start Smoothie for Hepatitis A

    Rader Farms Organic Fresh Start Smoothie, a frozen fruit and vegetable blend, has been recalled due to potential Hepatitis A contamination. The recall affects 62,380 bags distributed across 31 states.

    Product
    Rader Farms Organic Fresh Start Smoothie Blueberry, Strawberry, Raspberry, Kale, Spinach. Item # 1399671. Frozen, packed into 8oz. flexible plastic pouches and six 8oz pouches are packed into one flexible plastic bag. Net Wt. 48oz. UPC on retail bag: 8 84038 08326 2. A total…
    Category
    Food
    Distribution
    32 states