The Recall Desk

State

Northern Mariana Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37276–37300 of 73761

  • ModerateFDA (Devices)·Z-2750-2018·2018-08-22

    Terumo CDI Blood Parameter Monitoring System 500 H/SAT Recalled for Self-Test Failures

    Terumo is recalling 128 CDI Blood Parameter Monitoring System 500 H/SAT units because a hybrid intensity shift causes the automated Color Chip Test to fail, disabling the H/Sat module.

    Product
    CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous, on-line monitoring of the extracorporeal partial pressure of oxygen and carbon dioxide, pH, potassium, oxygen saturation, hematocrit, hemoglobin and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1814-2018·2018-08-22

    Confidence Nitro-Cross 60s Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Nitro-Cross 60s supplements due to undeclared ingredients including HPMC and Titanium Dioxide.

    Product
    FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2748-2018·2018-08-22

    Siemens ARTIS Pheno X-Ray System Recalled for Potential Hardware Thermal Issue

    Siemens Medical Solutions USA is recalling 605 ARTIS Pheno interventional fluoroscopic X-ray systems due to a potential hardware issue that may cause thermal effects and damage to system parts.

    Product
    ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1079-2018·2018-08-22

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures

    Dr. Reddy's is recalling 40 mg Atorvastatin Calcium tablets because stability testing showed impurity levels exceeding specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2742-2018·2018-08-22

    Merit Medical Systems Recalls 1mL Medallion Syringes Due to Plunger Defect

    Merit Medical Systems is recalling 22,234 units of 1mL Medallion Syringes due to a manufacturing defect in the plunger tip.

    Product
    1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2822-2018·2018-08-22

    Nico Corp. Recalls Mislabeled Sterile Shepherd's Hook Accessories

    Nico Corp. is recalling 204 sterile Shepherd's Hook accessories because they were shipped with incorrect transport labels instead of product labels.

    Product
    NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1099-2018·2018-08-22

    FDA Recalls Contrave Tablets Due to Punctured Bottle Complaints

    Orexigen Therapeutics is recalling 95,296 bottles of Contrave extended-release tablets due to customer complaints of punctures in the bottles.

    Product
    CONTRAVE — CONTRAVE (NALTREXONE HYDROCHLORIDE AND BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2749-2018·2018-08-22

    Richard-Allan Scientific Recalls Mislabeled EZ Single Cytofunnel Brown Units

    Richard-Allan Scientific is recalling 1,039 cases of EZ Single Cytofunnel Brown units due to mislabeling. The recall is voluntary and nationwide.

    Product
    EZ Single Cytofunnel Brown, A78710004 Product Usage: The EZ Single Cytofunnel with Brown filter papter are intended for single use with the Thermo Scientific Cytospin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1813-2018·2018-08-22

    Confidence Glucosamine Plus Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.

    Product
    FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891 02253 7
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2786-2018·2018-08-22

    Clarity 10SG Urinalysis Strips Recalled for Analyzer Incompatibility

    Clarity Diagnostics is recalling specific lots of Clarity 10SG Urinalysis Strips because they lack a Canister Code Bar Code Label, making them incompatible with Clarity Urocheck 120 Urine Analyzers.

    Product
    Clarity Urocheck 10SG Urinalysis Strips, Model # DTG-10SG Product Usage: Clarity 10SG Urinalysis Reagent Strips (Urine) are for the qualitative and semi-quantitative detection of the following analytes in urine: Glucose, Bilirubin, Ketone (Acetoacetic acid), Specific…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1816-2018·2018-08-22

    Confidence Glucosamine Plus Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.

    Product
    FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid + Curcumin & Boswellia, 60 Extended Release Tablets, UPC: 8 92483 00106 9
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·18198·2018-08-21

    Confer Plastics Recalls Pool Step Systems Due to Entrapment Hazard

    Confer Plastics is recalling Curve in-pool step systems because children's limbs can become entrapped in side openings, posing a drowning risk.

    Product
    Curve in-pool step systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V551000·2018-08-21

    Nissan and Chevrolet Recall for Ignition Switch Stalling Risk

    Nissan is recalling 2017-2018 models including the Versa, Sentra, and NV200 because the ignition switch may shift, causing the engine to stall and increasing crash risk.

    Product
    NISSAN — NISSAN, CHEVROLET VERSA NOTE, NV200 TAXI, VERSA, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V548000·2018-08-20

    Ford Recalls 2018-2019 Vehicles for Electrical Arc Fire Risk

    Ford is recalling 2018-2019 Edge, Flex, MKX, and MKT vehicles because improperly secured power supply cables may cause an electrical arc, increasing the risk of a fire.

    Product
    FORD — FORD, LINCOLN EDGE, MKX, MKT, FLEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V537000·2018-08-20

    Volkswagen Recalls 2018 Atlas Vehicles Due to Air Bag Control Module Risk

    Volkswagen is recalling 2018 Atlas vehicles because a twisted air conditioning drain tube may allow water to enter the air bag control module, potentially causing unintentional air bag deployment.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E085000·2018-08-20

    Allison Transmission Recall for Potential Loss of Drive

    Allison is recalling certain H 50 and H 40 Drive Units because pressure switches may fail, causing a loss of drive and increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V545000·2018-08-17

    2019 Coachmen Freedom Express Recalled for Brake Wiring Defect

    Forest River is recalling 2019 Coachmen Freedom Express trailers because the break-away safety switch may not engage brakes if the trailer detaches.

    Product
    COACHMEN — COACHMEN FREEDOM EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V546000·2018-08-17

    Winnebago Recalls 2016-2019 Motorhomes Due to Unfused Solar Charging Circuit

    Winnebago is recalling 2016-2019 motorhomes because an unfused auxiliary solar charging circuit can increase the risk of fire if solar panels exceed the circuit's amperage capacity.

    Product
    WINNEBAGO — WINNEBAGO TREND, PASEO, JOURNEY, ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18760·2018-08-17

    Polaris Recalls ACE 150 and Ranger 150 Vehicles Due to Crash Hazard

    Polaris is recalling about 5,900 ACE 150 and Ranger 150 recreational off-highway vehicles because the front suspension lower ball joint can separate, posing a crash hazard.

    Product
    Model year 2017-2018 Polaris ACE 150 and model year 2018 Polaris Ranger 150 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V539000·2018-08-16

    Mercedes-Benz Recalls 2018 GLE and GLS Models for Brake Defect

    Mercedes-Benz is recalling 9,044 2018 GLE and GLS vehicles because rear brake caliper pistons may release gas, reducing braking performance.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 450, AMG GLE63S, GLS 550, GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V542000·2018-08-16

    Volvo Recalls 2019 VNL and VNR Trucks for Fifth Wheel Defect

    Volvo is recalling 2019 VNL and VNR trucks because a narrow fifth wheel bracket may allow the trailer to separate from the tractor, increasing crash risk.

    Product
    VOLVO — VOLVO VNL, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V543000·2018-08-16

    Mack Recalls 2019 Anthem Trucks Due to Fifth Wheel Bracket Defect

    Mack Trucks is recalling 2019 Anthem trucks with Jost fifth wheel couplings because a narrow slider bracket may allow the trailer to separate, increasing crash risk.

    Product
    MACK — MACK ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide