The Recall Desk

State

North Dakota product recalls

72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2601–2625 of 75840

  • HighFDA (Devices)·Z-1596-2026·2026-04-01

    I.T.S. pilon and tibia plates heat more in MRI than stated

    I.T.S. GmbH is recalling Pilon Plates with Angular Stability and Anterolateral Tibia Plates because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.

    Product
    Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral Tibia Plate; Article Numbers: 21311-11, 21311-15, 21311-7, 21312-11, 21312-15, 21312-7. 2. Pilon Plate 4mm; Article Numbers: 21094-10, 21094-4, 21094-6, 2109
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1634-2026·2026-04-01

    TECNIS Eyhance intraocular lens haptic may stick to the optic

    AMO Puerto Rico Manufacturing is recalling TECNIS Eyhance IOLs with the TECNIS Simplicity Delivery System because a limited quantity may have a haptic that sticks to the optic, preventing consistent unfolding.

    Product
    Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Model/Catalog Number: DIB00 Software Version: N/A Product Description: The TECNIS SIMPLICITY" Delivery System is designed to provide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0596-2026·2026-04-01

    Ajinomoto Ling Ling Fried Rice Recalled for Glass Contamination

    Ajinomoto Foods North America is recalling Item 81097 Ling Ling Restaurant Style Fried Rice due to glass fragments measuring 1-3 cm long and 2-4 mm wide found in the product. Affected units with Best By dates 9/21/2026 through 3/8/2027 were distributed across 40 U.S. states.

    Product
    Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexib
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·H-0599-2026·2026-04-01

    Ajinomoto Green Gyoza Vegetable Edamame Dumplings Recalled for Glass

    Ajinomoto Foods North America Inc. is recalling Ajinomoto Green Gyoza Vegetable & Edamame Dumplings due to the presence of glass fragments (1–3 cm long and 2–4 mm wide) in the product.

    Product
    Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12ct. Retail bag UPC: None. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/12ct. bags per case. Case UPC 10071757080246. All products are intended to
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-1601-2026·2026-04-01

    I.T.S. fibula and tubular plates heat more in MRI than stated

    I.T.S. GmbH is recalling the Fibula Plate PROlock with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers. 1. Distal Tubular Plate; Article Numbers: 21602-3, 21602-4, 21602-5, 21602-6, 21602-7, 21602-8, 21603-3, 21603-4, 21603-5, 21603-6, 21603-7, 21603-8. 2. Fibul
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1630-2026·2026-04-01

    Orthalign knee drill plates may allow a bone cut exceeding specification

    Orthalign is recalling one lot of the Trimax Pegged Drill Plate for the Lantern Knee System because plates manufactured out of specification can result in a bone cut in excess of 0.0800 inches.

    Product
    Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V209000·2026-04-01

    Audi Q3 recalled over remote sunroof closing from out of sight

    Volkswagen Group of America is recalling 6,077 Audi Q3 vehicles because incorrect software may allow remote sunroof closing from a distance where the operator cannot clearly see the sunroof.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1633-2026·2026-04-01

    Straumann angled custom abutments made from wrong bar material

    Straumann is recalling Custom Abutment AS Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.

    Product
    Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0592-2026·2026-04-01

    Trader Joe's Vegetable Fried Rice recalled for glass fragments

    Ajinomoto Foods North America Inc. is recalling Trader Joe's Vegetable Fried Rice (1 lb bags, Item 5650233) due to glass fragments (1–3 cm long, 2–4 mm wide) found in the product. The recall affects approximately 9.9 million pounds distributed across 40 US states.

    Product
    Item 5650233 Trader Joe's Vegetable Fried Rice, net wt. 1lb per bag. Retail bag UPC 00521482. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per case. Case UPC 10052148200001. All products are intended t
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·H-0601-2026·2026-04-01

    Ajinomoto Vegetable Gyoza Dumplings Recalled for Glass Contamination

    Ajinomoto Foods North America Inc. is recalling Ajinomoto Vegetable Gyoza Dumplings due to the presence of glass fragments in the product. The recalled dumplings were distributed nationwide.

    Product
    Item 6430153 Ajinomoto Vegetable Gyoza Dumplings. Net wt. 24.7oz. per bag. Retail box UPC: 071757010109. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 8/24.7oz bags or 12.34lb. per case. Case UPC 10071757010106. All
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-1644-2026·2026-04-01

    Olympus PKS cutting forceps jaws may break from defective welds

    Olympus is recalling PKS Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.

    Product
    Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visuali
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1638-2026·2026-04-01

    Olympus Everest bipolar forceps model 3005 jaws may break

    Olympus is recalling Everest Bipolar Cutting Forceps model 3005 because a supplier did not adequately validate the welding process, and defective welds can cause the jaw to break during clinical use.

    Product
    Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3005 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved u
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1611-2026·2026-04-01

    Olympus endoscope air water valves no longer compatible with named reprocessors

    Olympus is recalling the MAJ-1444 Endoscope Air/Water Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

    Product
    Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1604-2026·2026-04-01

    I.T.S. distal ulna plates heat more in MRI than instructions state

    I.T.S. GmbH is recalling the Distal Ulna Locking and Ulna Osteotomy Locking Systems because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.

    Product
    I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and corresponding article numbers. 1. I.T.S. DUL (Distal Ulna Locking) System, Distal Ulna Plate; Article Numbers: 21232-3, 21232-4, 21232-6, 21233-3, 21233-4, 21233-6, 21
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1592-2026·2026-04-01

    I.T.S. volar radius plates heat more in MRI than stated

    I.T.S. GmbH is recalling Volar Radius Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0597-2026·2026-04-01

    Ajinomoto Tai Pei Shrimp Fried Rice Recalled for Glass Contamination

    Ajinomoto Foods North America Inc. is recalling Tai Pei Shrimp Fried Rice due to glass fragments found in the product. Glass pieces measuring 1–3 cm long and 2–4 mm wide pose a choking and injury risk.

    Product
    Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48oz or 3lbs. per box. Retail box UPC 070077811465. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 4
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·H-0598-2026·2026-04-01

    Kroger Chinese Inspiration Vegetable Fried Rice recalled for glass

    Ajinomoto Foods North America Inc. is recalling Kroger Chinese Inspiration Vegetable Fried Rice due to the presence of glass fragments varying from 1–3 cm long and 2–4 mm wide.

    Product
    Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice - Blend of long grain rice assorted vegetables & egg. Net wt. 22oz. Retail box UPC 011110041623. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 6/22oz. boxes o
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-1590-2026·2026-04-01

    GE Imactis CT navigation may show needle trajectory that differs from actual

    GE Medical Systems is recalling the Imactis CT-Navigation System because of a potential discordance between the simulated needle trajectory and tip position and the actual trajectory and tip position.

    Product
    Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1607-2026·2026-04-01

    I.T.S. hand locking plates heat more in MRI than instructions state

    I.T.S. GmbH is recalling the HLS Hand Locking Plates System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers. 1. Cortical Screw; Article Numbers: 32151-6, 32151-8, 32151-9, 32151-10, 32151-11, 32151-12, 32151-13, 32151-14, 32151-15, 32151-16, 32151-18, 32151-20. 2. HLS Plate, 2 T-Shape
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V208000·2026-04-01

    Volvo trucks recalled over turn signals that may not function properly

    Volvo Trucks North America is recalling 340 VNL and VNR vehicles because the turn signals may not function properly, failing to comply with the federal lighting standard.

    Product
    VOLVO — VOLVO VNL (4), VNR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1600-2026·2026-04-01

    I.T.S. pelvic reconstruction screws heat more in MRI than stated

    I.T.S. GmbH is recalling the Pelvic Reconstruction System fixation screw and short spike because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.

    Product
    Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw; Article Number: 70312. 2. Spike short; Article Number: 70314.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1610-2026·2026-04-01

    Olympus endoscope suction valve no longer compatible with named reprocessors

    Olympus is recalling the MAJ-1443 Endoscope Suction Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

    Product
    Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1606-2026·2026-04-01

    I.T.S. headless compression screws heat more in MRI than stated

    I.T.S. GmbH is recalling the HCS Headless Compression Screw System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated; Article Numbers: 31207-10, 31207-12, 31207-14, 31207-16, 31207-18, 31207-20, 31207-24, 31207-26, 31207-28, 31207-30, 31257-12, 31257-14, 31257-16, 31257-18, 31257-20, 31257-22, 31257-24, 31257-28, 31
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1612-2026·2026-04-01

    Olympus OER-Elite reprocessor no longer compatible with two valve models

    Olympus is recalling the OER-Elite Endoscope Reprocessor because the MAJ-1443 and MAJ-1444 air/water valves are no longer reprocessing compatible with the OER-Pro and OER-Elite reprocessors.

    Product
    Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1593-2026·2026-04-01

    I.T.S. clavicle plates heat more in MRI than instructions state

    I.T.S. GmbH is recalling Clavicula Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10. 2. Clavicle Plate; Article Numbers: 21121-6, 21121-8. 3. Clavicle Plate, 3.5mm; Article
    Category
    Medical Device
    Distribution
    Distributed nationwide