The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53651–53675 of 73850

  • HighNHTSA·15V326000·2015-05-29

    Genie TZ-34/20 Trailers Recalled for Outrigger Drift Risk

    Genie is recalling 2015 TZ-34/20 trailers because out-of-specification cylinders may cause outriggers to drift, increasing the risk of tip-over and injury.

    Product
    GENIE — GENIE TZ-34/20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15V318000·2015-05-28

    BMW Recalls 2002-2006 Models for Driver Air Bag Inflator Rupture Risk

    BMW is recalling specific 2002-2006 models because moisture can cause the driver's air bag inflator to rupture, potentially sending metal fragments into the cabin during a crash.

    Product
    BMW — BMW 325XI, 325I, 325CI, 330CI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15V320000·2015-05-28

    Honda and Acura Recall Vehicles for Air Bag Inflator Rupture Risk

    Honda is recalling specific 2001-2011 Honda and Acura vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    ACURA — ACURA, HONDA MDX, ACCORD, CIVIC, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V324000·2015-05-28

    GM Recalls 2007-2008 Trucks for Passenger Air Bag Inflator Defect

    General Motors is recalling 2007-2008 Chevrolet and GMC trucks because the passenger air bag inflator may rupture during deployment, potentially causing serious injury.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SIERRA 2500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V323000·2015-05-28

    Subaru and Saab Recall Vehicles for Airbag Inflator Rupture Risk

    Subaru and Saab are recalling specific 2003-2008 models because moisture can cause the passenger airbag inflator to rupture, potentially sending metal fragments into the cabin.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V319000·2015-05-28

    Ford Recalls Mustang and GT Vehicles for Air Bag Defect

    Ford is recalling 2005-2014 Mustangs and 2005-2006 GTs because the driver's air bag inflator may rupture in a crash, posing a risk of serious injury or death.

    Product
    FORD — FORD GT, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15151·2015-05-28

    Mason Jar Night Light Recalled Due to Burn Hazard

    Nantucket Distributing is recalling Mason Jar Night Lights because the plastic base can melt, posing a burn hazard. No injuries have been reported.

    Product
    Mason Jar Night Light
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15152·2015-05-28

    GT Fury Mountain Bicycles Recalled Due to Front Wheel Hub Failure Risk

    Cycling Sports Group is recalling 2015 GT Fury Elite and Expert downhill mountain bicycles because the front wheel hub can break, causing disc brake failure and crash hazards.

    Product
    GT downhill mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1641-2015·2015-05-27

    Ethicon Endo-Surgery Recalls Echelon Vascular White Reloads Due to Staple Line Defect

    Ethicon Endo-Surgery is recalling 6,744 Echelon Vascular White Reloads because an internal inspection found a production issue that may cause the cartridge to deploy an incomplete staple line.

    Product
    ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic and pediatric surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2314-2015·2015-05-27

    Waymouth Farms Recalls Raw Pine Nuts Due to Salmonella Risk

    Waymouth Farms is recalling specific brands and sizes of raw pine nuts because they may be contaminated with Salmonella.

    Product
    Raw Pine Nuts sold in the following brands and package sizes: -Good Sense 3 oz. (85g) bag UPC 30243-86681, -Good Sense 4 oz. (113g) bag, UPC 30243-86680, -Good Sense 4 oz. (113g) tub UPC 30243-50799, -Good Sense 15 oz. (425g) bag UPC 30243-86687, -Good Sense 5…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V316000·2015-05-27

    Eldorado Axess, XHF, and E-Z Rider II Recalled for Engine Fire Risk

    Eldorado is recalling 2007-2015 Axess, XHF, and E-Z Rider II vehicles because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    ELDORADO — ELDORADO AXESS, XHF, E-Z RIDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V317000·2015-05-27

    Keystone and Dutchmen Recalling 2015 Fifth Wheels for Expanding Room Defect

    Keystone RV Company is recalling 2015 Keystone and Dutchmen fifth wheels because screws securing the expanding room may fail, increasing crash risk.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE KODIAK, AEROLITE, CARBON, ALPINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2185-2015·2015-05-27

    Superior Foods Recalls Organic Chopped Spinach Due to Possible Listeria Contamination

    Superior Foods is recalling Simply Balanced Organic Chopped Spinach due to possible Listeria contamination. Consumers should not eat the product and should return it to the store.

    Product
    Simply Balanced Organic Chopped Spinach NET WT 10 OZ (283g) steam-in-bag Needs to be fully cooked Keep frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1643-2015·2015-05-27

    Philips Pinnacle3 Software Recall Due to Incorrect Dose Calculation

    Philips Medical Systems is recalling Pinnacle3 software version 10.0 because a defect in the dose engine may cause incorrect radiation therapy dose calculations.

    Product
    Pinnacle3 Software Version 10.0, Model 459800200841. Product Usage: The Pinnacle 3 RTP software allows qualified medical professionals to enter patient data into the system, use that data to construct a plan for radiation therapy and evaluate the plan. Optionally, the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V314000·2015-05-27

    Crane Carrier Recalls 2008-2015 Trucks Due to Engine Fire Risk

    Crane Carrier is recalling 630 model year 2008-2015 COE, LDT2, and LET2 trucks because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    CRANE — CRANE COE, LET2, LDT2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1639-2015·2015-05-27

    Richard Allan Scientific Recalls Mucolytic Agent Due to Fungal Contamination

    Richard Allan Scientific is recalling Mucolytic Agent and Mucolexx after a customer complaint reported fungal contamination in two lots of Mucolexx.

    Product
    Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus and allows for optimal cytologic diagnostic results.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1628-2015·2015-05-27

    Baxter ABACUS Software Recalled for Potential TPN Formula Loading Errors

    Baxter is recalling ABACUS SE and ME software because it may load incorrect total parenteral nutrition formulas when duplicate order numbers are used.

    Product
    ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation Edition) Product Usage: The ABACUS Software is a Windows-based order entry software application for comprehensive total parenteral nutrition (TPN) calculations and label printing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1642-2015·2015-05-27

    DeRoyal Specimen Retrieval Bags Recalled for Tearing During Use

    DeRoyal Industries is recalling 5,359 Medium Specimen Retrieval Bags because they may tear or come apart during laparoscopic procedures.

    Product
    DeRoyal(R) Medium Specimen Retrieval Bag, REF 5500-000-003, Rx Only Product Usage: The device is a single-use specimen retrieval bag indicated for use in laparoscopic procedures to capture and remove organs or tissue from the body cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1622-2015·2015-05-27

    Roche Homocysteine Test System Recalled for Inaccurate Low Results

    Roche Diagnostics is recalling Homocysteine Reagent lots due to complaints of under-recovery and falsely low patient results, which could delay diagnosis of peripheral vascular disease.

    Product
    Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA Homocysteine Enzymatic Assay is an in vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V315000·2015-05-27

    Toyota Recalls 2015 Tundra for Incorrect Tire Pressure Placard

    Southeast Toyota Distributors is recalling 144 model year 2015 Toyota Tundra vehicles because the tire placard lists incorrect inflation pressure, which could lead to underinflation and tire failure.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1640-2015·2015-05-27

    Richard-Allan Scientific Recalls Mucolexx Mucolytic Agent Due to Fungal Contamination

    Richard-Allan Scientific is recalling Mucolexx mucolytic agent and Mucolexx products after a customer reported fungal contamination in two lots.

    Product
    Lerner Laboratories Mucolexx, 1 pint / 473 ml & 1 gallon/3.8 L; Shandon Mucolexx 500ml/0.13gal, 4L/1.06 gal, 120mL Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1634-2015·2015-05-27

    Stryker Scorpio femoral component recall due to blister seal strength

    Stryker Howmedica Osteonics is recalling 1,147 Scorpio femoral components because the inner blister peel strength may be below validated requirements, potentially affecting sterile barrier shelf life.

    Product
    Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint.
    Category
    Medical Device
    Distribution
    Distributed nationwide