The Recall Desk

State

Northern Mariana Islands product recalls

73,806 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total
23
Critical
0
Severe
18
Most recent
2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43051–43075 of 73829

  • HighNHTSA·17V358000·2017-06-05

    Hyundai Recalls 2013-2017 Santa Fe Models for Hood Latch Defect

    Hyundai is recalling 2013-2017 Santa Fe and Santa Fe Sport vehicles because the secondary hood latch cable may corrode, potentially allowing the hood to open while driving.

    Product
    HYUNDAI — HYUNDAI SANTA FE, SANTA FE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V364000·2017-06-05

    Mercedes-Benz Sprinter 2500 and 3500 Tire Label Recall

    Daimler Vans USA is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vehicles because the B-pillar tire labels list incorrect, low tire pressures.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V362000·2017-06-02

    Thor Motor Coach Recalls 2017 Challenger 37YT Motorhomes for Exhaust Defect

    Thor Motor Coach is recalling 2017 Challenger 37YT motorhomes because the generator exhaust pipe may be mislocated or missing, creating a carbon monoxide risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V360000·2017-06-02

    MCI Recalls 2014-2017 J4500 Motor Coaches Due to Brake Hose Defect

    Motor Coach Industries is recalling 2014-2017 J4500 motor coaches because over-tightened front brake hose clamps may damage the hoses, potentially increasing stopping distance and crash risk.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V355000·2017-06-01

    Mazda Recalls 2004 RX-8 Vehicles for Front Suspension Control Arm Defect

    Mazda is recalling 2004 RX-8 vehicles because a crack in the front suspension lower control arm ball joint socket may cause the ball joint to separate, potentially leading to loss of steering control.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V357000·2017-06-01

    Polaris Recalls 2015-2017 Slingshot Vehicles for Missing Swingarm Grommets

    Polaris is recalling 2015-2017 Slingshot vehicles because missing grommets on replacement swingarms may allow debris to contaminate the rear wheel speed sensor, disabling ABS and traction control.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V356000·2017-06-01

    Toyota Recalls 2016-2017 Tacoma Vehicles Due to Engine Stall Risk

    Toyota is recalling 2016-2017 Tacoma vehicles with six-cylinder engines because a faulty crank position sensor may cause the engine to stall, increasing crash risk.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0864-2017·2017-05-31

    Hyland's Baby Nighttime Teething Tablets Recalled for Inconsistent Belladonna Alkaloids

    Standard Homeopathic Company is recalling Hyland's Baby Nighttime Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids.

    Product
    Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated), Calcarea Phosphorica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Magnesia Phosphorica 6X HPUS, Rheum 6X HPUS, Silicea 12X HPUS] Quick-Dissolving Tablets, 135-count…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2266-2017·2017-05-31

    Huson Valley Farms Recalls Cashew Butter for Listeria Contamination

    Huson Valley Farms is recalling 5,022 jars of Nutty INFUSIONS Roasted Cashew Butter due to Listeria monocytogenes contamination. The product was distributed nationwide through a wholesale in Illinois.

    Product
    Nutty INFUSIONS Roasted Cashew Butter, NET WT. 10 OZ (284 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0863-2017·2017-05-31

    Hyland's Baby Teething Tablets Recalled for Inconsistent Belladonna Alkaloid Levels

    Standard Homeopathic Company is recalling Hyland's Baby Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from label claims.

    Product
    Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated)] Quick-Dissolving Tablets, packaged in a) 40-count bottles (NDC 54973-3127-3) (UPC 3 54973 31273 9); b) 135-count…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0867-2017·2017-05-31

    Envy Me Recalls LaBri's Body Health Atomic Due to Undeclared Sibutramine

    Envy Me is recalling LaBri's Body Health Atomic capsules because the product contains undeclared Sibutramine and was marketed without an approved NDA/ANDA.

    Product
    LaBri's Body Health Atomic, 60 capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2269-2017·2017-05-31

    Nutty INFUSIONS Ginger Wasabi Cashew Butter Recalled for Listeria Contamination

    Huson Valley Farms is recalling Nutty INFUSIONS Ginger Wasabi Cashew Butter due to Listeria monocytogenes contamination. The product was distributed nationwide through a wholesale in Illinois.

    Product
    Nutty INFUSIONS Ginger Wasabi Cashew Butter, NET WT. 10 OZ (284 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0862-2017·2017-05-31

    Hospira Recalls Dextrose Injection Syringes Due to Human Hair Particulate

    Hospira is recalling 71,550 syringes of Infant 25% Dextrose Injection because human hair was found in an internal sample. The product was distributed nationwide and in Puerto Rico.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2119-2017·2017-05-31

    EBI Patient Care Recalls SpF-PLUS Implantable Stimulators Due to Cytotoxicity

    EBI Patient Care, Inc. is recalling 33 SpF-PLUS Implantable Stimulators due to higher than allowed cytotoxicity levels found during routine process monitoring.

    Product
    10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V351000·2017-05-31

    Spartan Recalls 2010-2014 Chassis Due to Starter Motor Fire Risk

    Spartan Motors is recalling 2010-2014 K2, K3, and Gladiator chassis because a starter motor component may break, causing overheating and increasing fire risk.

    Product
    SPARTAN — SPARTAN K3, GLADIATOR, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2236-2017·2017-05-31

    Lords Organics Recalls Ginger Powder Due to Salmonella Contamination Risk

    Lords Organics is recalling Organic Veda brand Ginger Powder because it may be contaminated with Salmonella. The recall covers 96 units distributed nationwide.

    Product
    Organic Veda brand Ginger Powder, 24 jars, Net Wt. 16 oz. (454 grams)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V349000·2017-05-31

    Pierce Fire Trucks Recalled for Rear Sway Bar Detachment Risk

    Pierce Manufacturing is recalling 2012-2017 fire trucks because a rear sway bar may detach, increasing crash risk during steering.

    Product
    PIERCE — PIERCE ARROW XT, QUANTUM, DASH, ENFORCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2118-2017·2017-05-31

    EBI Patient Care Recalls Spinal Fusion Stimulators Due to Cytotoxicity

    EBI Patient Care is recalling 33 SpF-XL IIB implantable stimulators because routine monitoring found higher than allowed cytotoxicity levels.

    Product
    10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2017·2017-05-31

    Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Round Drains

    Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing the risk of infection.

    Product
    Jackson-Pratt Hemaduct Silicone Round Drain, 15FR W/15FR Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain…
    Category
    Medical Device
    Distribution
    Distributed nationwide