The Recall Desk

State

North Dakota product recalls

72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3176–3200 of 75857

  • HighFDA (Devices)·Z-1348-2026·2026-02-18

    Azurion 7 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V094000·2026-02-18

    2025 Lexus LX vehicles recalled for transmission control software defect

    Toyota is recalling certain 2025-2026 Lexus LX600 vehicles due to a potential transmission solenoid failure that can damage the transmission, causing loss of drive power or fluid leaks that increase crash and fire risk.

    Product
    LEXUS — LEXUS LX, LS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1318-2026·2026-02-18

    Spectral CT 7500 scanners recalled over rotor fasteners that may loosen

    Philips is recalling 3 units of the Spectral CT 7500 on Rails because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.

    Product
    Spectral CT 7500 on Rails; Product Code (REF): 728334;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0502-2026·2026-02-18

    Peanut butter cups recalled over blue plastic found in a filter

    Ventura Foods is recalling 17 after the firm found pieces of blue plastic in a filter during production.

    Product
    CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET WT 0.75OZ DIST BY: DYMA BRANDS, INC. ATLANTA, GA 30328; Product also sold under the following brand names: FLAVOR Fresh PEANUT BUTTER NET WT 0.75 OZ(21g) DISTR
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1316-2026·2026-02-18

    IQon Spectral CT recalled over rotor fasteners that may be undertorqued

    Philips is recalling 52 IQon Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.

    Product
    IQon Spectral CT; Product Code (REF): 728332;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0318-2026·2026-02-18

    Testosterone 25mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 89,074 pellets of Testosterone, 25.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 25.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1025-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0334-2026·2026-02-18

    Ketamine injection bags recalled over a lack of assurance of sterility

    Fresenius Kabi Compounding is recalling 1,410 bags of Ketamine HCl injection over a lack of assurance of sterility.

    Product
    ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2026·2026-02-18

    PowerGlide and central line kits recalled over open swabstick seals

    Medline is recalling 7,380 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1339-2026·2026-02-18

    GammaPlan 11.1 recalled over plans that may irradiate the wrong location

    Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.

    Product
    Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2026·2026-02-18

    Suture removal trays recalled over open swabstick applicator seals

    Medline is recalling 2,448 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1328-2026·2026-02-18

    Pediatric catheter securement kits recalled over open swabstick seals

    Medline is recalling 450 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0329-2026·2026-02-18

    Testosterone 200mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 7,840 pellets of Testosterone 200mg, Triamcinolone Acetonide 40mcg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone 200mg, Triamcinolone Acetonide 40mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6200-43.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1326-2026·2026-02-18

    Anesthesia artline packs recalled over open swabstick applicator seals

    Medline is recalling 120 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0309-2026·2026-02-18

    Estradiol 12.5mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 22,478 pellets of ESTRADIOL, 12.5 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 12.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79599-3012-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0317-2026·2026-02-18

    Testosterone 18mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 146 pellets of Testosterone, 18.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 18.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1018-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1349-2026·2026-02-18

    Azurion 7 M20 systems recalled over tables that may move unexpectedly

    Philips is recalling 5 of the Azurion 7 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0320-2026·2026-02-18

    Testosterone 50mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 70,959 pellets of Testosterone, 50.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 50.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1050-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0307-2026·2026-02-18

    Estradiol 6mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 50,990 pellets of ESTRADIOL, 6 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 6 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3006-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1336-2026·2026-02-18

    Circumcision trays recalled over open swabstick applicator seals

    Medline is recalling 168 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1350-2026·2026-02-18

    Azurion 5 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 326 units of the Azurion 5 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0314-2026·2026-02-18

    Estradiol 25mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 2,442 pellets of ESTRADIOL, 25 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 25 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3025-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0326-2026·2026-02-18

    Testosterone and anastrozole 4.5 pellets recalled over metal particulate matter

    Asteria Health is recalling 100 pellets of Testosterone 100mg, Anastrozole 4mg (4.5) sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone 100mg, Anastrozole 4mg (4.5), 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1333-2026·2026-02-18

    Blood culture kits recalled over open swabstick applicator seals

    Medline is recalling 4,300 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1344-2026·2026-02-18

    Azurion 3 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 291 units of the Azurion 3 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide