The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58826–58850 of 73856

  • SevereNHTSA·14V181000·2014-03-31

    Jaguar Recalls 2013-2014 XF Models Due to Loose Charge Air Cooler Hose Clamp

    Jaguar is recalling 2013-2014 XF 2.0L GTDi vehicles because a loose hose clamp may allow the Charge Air Cooler hose to detach, potentially causing the engine to stall and loss of steering and brake assistance.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V157000·2014-03-31

    Jaguar Recalls 2013-2014 XJ, XF, and XK for Rear Suspension Defect

    Jaguar is recalling 2013-2014 XJ, XF, and XK vehicles because rear toe links can separate, potentially causing loss of vehicle control and increasing crash risk.

    Product
    JAGUAR — JAGUAR XF, XJ, XK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V151000·2014-03-31

    GM Recalls 2013-2014 Chevrolet Cruze for Right Front Half Shaft Fracture Risk

    General Motors is recalling 2013-2014 Chevrolet Cruze vehicles with 1.4L turbo engines because the right front half shaft may fracture, potentially causing loss of power or unexpected vehicle movement.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V155000·2014-03-31

    Land Rover Recalls 2014 Range Rover Evoque for Rear Suspension Bolt Defect

    Land Rover is recalling 2014 Range Rover Evoque vehicles because damaged rear suspension bolts may fail, causing the link arm to separate and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E011000·2014-03-31

    Speedway Motors Recalls Brake Light Switches Due to Fluid Leak Risk

    Speedway Motors is recalling specific brake light switches used in hot rods that may crack, causing brake fluid leaks and increased stopping distances.

    Product
    EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V153000·2014-03-31

    GM Recalls 1.4 Million Vehicles for Electric Power Steering Loss

    General Motors is recalling approximately 1.4 million vehicles due to a potential sudden loss of electric power steering assist, which increases the risk of a crash.

    Product
    SATURN — SATURN, CHEVROLET, PONTIAC ION, MALIBU MAXX, MALIBU, G6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V163000·2014-03-31

    Land Rover Recalls 2014 Range Rovers for Turn Signal Software Defect

    Jaguar Land Rover is recalling 5,238 2014 Range Rovers because a software defect may prevent the turn signal indicator from flashing at a double rate to warn of a malfunction.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V158000·2014-03-31

    Mercedes-Benz Recalls 2014 GL Models for Child Seat Anchor Defect

    Mercedes-Benz is recalling 2014 GL350, GL450, GL550, and GL63 vehicles because the second-row seat may not fold low enough for proper child seat anchoring.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GL550, GL450, GL350, AMG GL63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V149000·2014-03-27

    Tiffany Coach Recalls 2009-2010 Buses Due to Electrical Fire Risk

    Tiffany Coach Builders is recalling 2009-2010 Coach, Limo, and Shuttle Buses because voltage spikes may damage electrical components, increasing the risk of a fire.

    Product
    TIFFANY — TIFFANY SHUTTLE BUS, COACH, LIMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1212-2014·2014-03-26

    Abbott Recalls FreeStyle Flash Blood Glucose Meters Due to Inaccurate Results

    Abbott Diabetes Care is recalling FreeStyle Flash Blood Glucose Monitors because they may produce inaccurate low blood glucose readings when used with specific test strips.

    Product
    FreeStyle Flash Blood Glucose Monitors System. Meter made in China; Distributed by TheraSense, Alameda, CA The FreeStyle Flash meter should only be used with FreeStyle Test Strips and FreeStyle Control Solution. Using other brands of test strips and control solutions…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1169-2014·2014-03-26

    Clalis capsules recalled for undeclared sildenafil ingredient

    Fabscout Entertainment, Inc. is recalling Clalis capsules because FDA analysis found they contain sildenafil, an undeclared active pharmaceutical ingredient.

    Product
    Clalis capsules, 50 mg, 6 -count bottle ( labeling is in foreign language)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1163-2014·2014-03-26

    Baxter Recalls Sodium Chloride IV Solutions Due to Particulate Matter

    Baxter Healthcare is voluntarily recalling 0.9% Sodium Chloride Injection IV solutions due to the presence of particulate matter, including fibers and plastic particles.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1170-2014·2014-03-26

    Silver Sword capsules recalled for undeclared sildenafil ingredient

    Fabscout Entertainment is recalling Silver Sword capsules because FDA analysis found they contain sildenafil, an undeclared active pharmaceutical ingredient.

    Product
    Silver Sword capsules, 180 mg, 16-count clamshell tin, UPC 1 234658 970128 12345 (labeling is in foreign language)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1160-2014·2014-03-26

    Baxter Recalls Clinimix IV Bags Due to Particulate Matter

    Baxter Healthcare is recalling 7,388 bags of Clinimix 5/15 sulfite-free IV solution because they contain particulate matter, including wood, sodium citrate, and dextrose.

    Product
    CLINIMIX — CLINIMIX (LEUCINE, PHENYLALANINE, LYSINE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, SERINE, TYROSINE, DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1158-2014·2014-03-26

    Baxter Recalls Clinimix E Bags Due to Particulate Matter

    Baxter Healthcare is recalling 14,574 bags of Clinimix E IV solution found to contain particulate matter, including wood, sodium citrate, and dextrose.

    Product
    CLINIMIX E — CLINIMIX E (LEUCINE, PHENYLALANINE, LYSINE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, SERINE, TYROSINE, DIBASIC POTASSIUM PHOSPHATE, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1211-2014·2014-03-26

    Abbott FreeStyle Blood Glucose Monitors Recalled for Inaccurate Results

    Abbott Diabetes Care is recalling FreeStyle Blood Glucose Monitors because they may produce inaccurate blood glucose readings when used with specific test strips.

    Product
    FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use only. Store at room temperature below 86 degrees F (30 degrees C). Use test strips only within the system operating temperature range as outlined in your Owner's Booklet. Meter made in China…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1159-2014·2014-03-26

    Baxter Recalls Clinimix E IV Bags Due to Particulate Matter

    Baxter Healthcare is recalling 7,068 bags of Clinimix E IV solution because they contain particulate matter, including wood, sodium citrate, and dextrose.

    Product
    CLINIMIX E — CLINIMIX E (LEUCINE, PHENYLALANINE, LYSINE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, SERINE, TYROSINE, DIBASIC POTASSIUM PHOSPHATE, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide