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.

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.

2551–2575 of 75840

  • SevereNHTSA·26E018000·2026-04-02

    Sleepy Customs Recalls IS300 Slave Cylinder Conversion Kits

    Sleepy Customs LLC is recalling IS300 Slave Cylinder Conversion Kits because the adapter plate may separate, causing loss of clutch function and increasing crash risk.

    Product
    POWER TRAIN:CLUTCH ASSEMBLY:SLAVE CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26377·2026-04-02

    Granitestone sauté pan handle screw caps can eject when heated

    E Mishan & Sons is recalling Granitestone Diamond Pro Blue sauté pans because the metal cap on the handle screw can detach and forcefully eject when heated. One injury has been reported.

    Product
    Granitestone Diamond Pro Blue Sauté Pans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V213000·2026-04-02

    Corvettes recalled over undetected rear turn signal light failures

    General Motors is recalling 32,988 Chevrolet Corvette vehicles because a software error may prevent detection of a rear turn signal light failure.

    Product
    CHEVROLET — CHEVROLET CORVETTE COUPE, CORVETTE CONVERTIBLE, CORVETTE CONVERTIBLE E-RAY, CORVETTE COUPE E-RAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26373·2026-04-02

    Ocun Condor carabiner gates may not close automatically after use

    OCUN NA is recalling Ocun Condor HMS Triple Locking Carabiners because the gate can malfunction and fail to close automatically, having to be closed by hand.

    Product
    Ocun Condor HMS Triple Locking Carabiners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26365·2026-04-02

    Beestech spiral tower toys contain small balls posing choking hazard

    Beestech spiral children's tower toys are being recalled because they contain small balls and are intended for children under three, violating the mandatory standard for toys.

    Product
    Beestech Children's Spiral Tower Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26369·2026-04-02

    Coluans Christmas light-up rings let children access button cell batteries

    Coluans Christmas Light-Up Rings party favors are being recalled because the battery compartment contains button cell batteries that can be easily accessed by children.

    Product
    Coluans Christmas Light-Up Rings Party Favors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26368·2026-04-02

    Gavoyeat Halloween light-up rings let children access button cell batteries

    Gavoyeat Halloween Light-Up Rings party favors are being recalled because the battery compartment contains button cell batteries that can be easily accessed by children.

    Product
    Gavoyeat Halloween Light-Up Rings Party Favors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26381·2026-04-02

    Tuymec minoxidil hair growth kits lack child-resistant packaging

    Tuymec Minoxidil Hair Growth Kits are being recalled because the packaging is not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.

    Product
    Tuymec Minoxidil Hair Growth Kits, 5% Minoxidil with Biotin Spray
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26374·2026-04-02

    ELENKER adult bed rails pose entrapment and asphyxiation hazard

    ELENKER-branded adult portable bed rails in three sizes are being recalled because users can become entrapped within the rail or between the rail and the mattress.

    Product
    ELENKER Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V214000·2026-04-02

    BMW motorcycles recalled over a reverse gear unit that may overheat

    BMW of North America is recalling 9,160 K 1600 motorcycles because a deteriorating seal can let moisture into the reverse gear control unit, causing it to overheat.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 GRAND AMERICA, K 1600 B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26375·2026-04-02

    TecFlox hair and beard serum bottles lack child-resistant packaging

    TecFlox hair and beard growth serum bottles are being recalled because they are not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.

    Product
    TecFlox Hair and Beard Growth Serum Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26378·2026-04-02

    Sangohe adult portable bed rails pose entrapment and asphyxiation hazard

    Sangohe adult portable bed rails models 504E and 504Q are being recalled because users can become entrapped within the rail or between the rail and the mattress.

    Product
    Sangohe Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1576-2026·2026-04-01

    ProGuide chronic dialysis catheters recalled as Class I over sheath introducer defect

    Merit Medical is recalling ProGuide Chronic Dialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.

    Product
    ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V210000·2026-04-01

    Isuzu and Chevrolet Commercial Trucks Recalled for Wire Harness Chafing

    Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.

    Product
    ISUZU — ISUZU CHEVROLET LCF 4500HD, NPR HD, CHEVROLET LCF 5500XD, NPR XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1566-2026·2026-04-01

    Erbe flexible cryoprobe 20402-401 recalled as Class I over rupture

    Erbe USA is recalling the Flexible Cryoprobe REF 20402-401 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.

    Product
    Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1579-2026·2026-04-01

    BioFlo DuraMax catheters recalled as Class I over sheath introducer defect

    Merit Medical is recalling BioFlo DuraMax Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.

    Product
    BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H965103028031/EU, H965103028041/A, H965103028041/EU, H965103028051/A, H965103028051/EU, H965103028061/A, H965103028061/EU, H965103028070/A, H965103028070/EU, H965103028080/A, H96510
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1588-2026·2026-04-01

    Heating pad recalled as Class I because folding causes excessive temperatures

    Navajo Manufacturing is recalling the Handy Solutions Neck & Shoulders Heating Pad because folding it during use raises power density in the folded area, causing excessive temperatures the limit device cannot sense.

    Product
    Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1617-2026·2026-04-01

    Trilogy Evo Universal ventilator recalled as Class I over tidal volume

    Philips Respironics is recalling the Trilogy Evo Universal ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.

    Product
    Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0591-2026·2026-04-01

    Trader Joe's Japanese Style Fried Rice recalled for glass fragments

    Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.

    Product
    Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb. per bag. Retail bag UPC 00979085. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per ca
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Food)·H-0593-2026·2026-04-01

    Ajinomoto Teppanyaki Style Vegetable Fried Rice recalled for glass fragments

    Ajinomoto Foods North America is recalling Teppanyaki Style Vegetable Fried Rice due to the presence of glass fragments ranging from 1–3 cm long. Consumers should not eat affected products and should discard or return them.

    Product
    Item 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice - Japanese-style fried rice made with colorful vegetables in an aromatic garlic butter sauce. There are 6/9oz. bags per box or 54oz per box. Retail box UPC 071757508835. Product packaging is flexible bags in a master c
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Devices)·Z-1577-2026·2026-04-01

    Merit 16F splittable sheath introducer recalled as Class I bulk product

    Merit Medical is recalling the 16F Dual Valved Splittable Sheath Introducer in bulk non-sterile form because a design defect may prevent it splitting as intended.

    Product
    16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B
    Category
    Medical Device
    Distribution
    Distributed nationwide