The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51626–51650 of 73847

  • HighNHTSA·15V636000·2015-10-09

    GM Recalls 2014 Chevrolet Caprice and SS for Airbag Deployment Risk

    General Motors is recalling 2014 Chevrolet Caprice and SS vehicles because a missing seat bracket may cause airbags to deploy with excessive force.

    Product
    CHEVROLET — CHEVROLET CAPRICE, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V637000·2015-10-09

    Ducati Recalls Multistrada Motorcycles Due to Side-Stand Defect

    Ducati is recalling 2015-2016 Multistrada 1200 and 1200 S motorcycles because the side-stand may break, causing the bike to fall over and increasing injury risk.

    Product
    DUCATI — DUCATI MULTISTRADA 1200S, MULTISTRADA 1200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V634000·2015-10-08

    Volvo Recalls VNL Trucks Due to APU Mounting Defect

    Volvo is recalling 2012-2014 VNL trucks because Electric Auxiliary Power Units may detach, creating a road hazard and increasing crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V632000·2015-10-08

    KME Predator Emergency Vehicles Recalled for Front Suspension Defect

    KME is recalling 2013-2015 Predator emergency vehicles because loose front ball joints may separate, causing loss of steering control and increasing crash risk.

    Product
    KME — KME PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V631000·2015-10-08

    Navistar Recalls 2016 International Trucks Due to Engine Stalling Risk

    Navistar is recalling specific 2016 International trucks because the engine control module may short circuit, causing the engine to stall without warning and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, LONESTAR, PAYSTAR, PROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16006·2015-10-08

    Safety 1st Recalls Décor Wood Highchairs Due to Fall Hazard

    Safety 1st is recalling about 35,000 Décor Wood highchairs because children can remove the tray, posing a fall hazard. The company has received 68 reports of tray removal, including 11 injuries.

    Product
    Décor Wood Highchair
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3251-2015·2015-10-07

    Ice Cream Club Recalls Caramel Caribou Ice Cream for Undeclared Peanuts

    The Ice Cream Club, Inc. is recalling Caramel Caribou Ice Cream because it contains undeclared peanuts, a major food allergen.

    Product
    Caramel Caribou Ice Cream, 3 gal, frozen in bulk round container.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·16005·2015-10-07

    Bed Handles Inc. Recalls Portable Bed Handles Due to Entrapment Deaths

    Bed Handles Inc. is recalling approximately 113,000 portable bed handles sold without safety retention straps. The recall follows reports of four deaths caused by entrapment in gaps between the handle and mattress.

    Product
    Portable bed handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V628000·2015-10-07

    BMW Recalls 2014-2016 MINI and i3 Vehicles for Air Bag Defect

    BMW is recalling specific 2014-2016 MINI and i3 vehicles because the passenger air bag may not deploy properly in a low-speed crash, increasing injury risk.

    Product
    MINI — MINI, BMW COOPER, I3, COOPER S, JOHN COOPER WORKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V629000·2015-10-07

    Hyundai Recalls 2011 Elantra and Sonata for Front Coil Spring Fracture Risk

    Hyundai is recalling 28,157 model year 2011 Elantra and Sonata vehicles because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.

    Product
    HYUNDAI — HYUNDAI ELANTRA, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2825-2015·2015-10-07

    Arrow Kits with Medtronic Syringes Recalled for Compromised Sterility

    Arrow International Inc. is recalling Arrow Kits containing Medtronic Covidien 0.9% Sodium Chloride Flush Syringes due to compromised sterility of the outer barrel.

    Product
    Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2743-2015·2015-10-07

    MicroPort Recalls Profemur Plus Modular Neck Hip Prosthesis Components

    MicroPort Orthopedics is recalling Profemur Plus modular neck hip prosthesis components due to an unexpected rate of postoperative fractures requiring revision surgery.

    Product
    PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V627000·2015-10-07

    Volkswagen Recalls 2015 Jetta, Golf, and E-Golf for Air Bag Defect

    Volkswagen is recalling 993 model year 2015 Jetta, Golf, and E-Golf vehicles because the passenger air bag may not deploy properly in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, E-GOLF, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1833-2015·2015-10-07

    Medistat RX Recalls Sterile Products Due to Sterility Assurance Concerns

    Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.

    Product
    All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave., Foley, AL 36535, 844*737*2550. An Incomplete List of Recalled Products Includes 1) All Cyanacobalamin Products, 2) All Magnesium Chloride Products, 3) All Lipostat (MIC B12) Products, 4) All Trimix…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3248-2015·2015-10-07

    General Mills Recalls Cascadian Farm Organic Cut Green Beans for Listeria

    General Mills is recalling specific lots of Cascadian Farm Organic Cut Green Beans because one package tested positive for Listeria monocytogenes.

    Product
    Cascadian Farm Organic Cut Green Beans, Net Wt. 10 oz (284g) Keep Frozen.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0003-2016·2015-10-07

    Biosense Webster Recalls SOUNDSTAR eco Diagnostic Ultrasound Catheters

    Biosense Webster is recalling SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters because the ultrasound image may disappear if the CARTO 3 system restarts during a pericardial effusion.

    Product
    SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2824-2015·2015-10-07

    Medtronic Navigated Solera Screwdrivers Recalled for Potential Tip Deformation

    Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.

    Product
    P/N: 9734856, SCREWDRIVER, 9734856, SOLERA STD MAST; P/N: 9734857, SCREWDRIVER, 9734857, SOLERA RDN MAST; P/N: 9734279, SCREWDRIVER 9734279 SOLERA STANDARD; and P/N: 9734373, SCREWDRIVER 9734373 SOLERA REDUCTION. The Medtronic Navigated Solera Screwdrivers are reusable devices…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0002-2016·2015-10-07

    Biosense Webster Recalls Carto 3 EP Navigation System Due to Image Loss

    Biosense Webster is recalling the Carto 3 EP Navigation System because the ultrasound image may disappear during use, requiring a system restart.

    Product
    Carto 3 EP Navigation System. Electro physiology system which views of the electrical activity of the heart through real-time data on 3-D, color-coded cardiac maps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V630000·2015-10-07

    Volvo Recalls 2015-2016 Trucks for Headlight Intensity Defect

    Volvo is recalling 2015-2016 VAH and VHD trucks because some headlights do not meet federal intensity requirements, increasing crash risk.

    Product
    VOLVO — VOLVO VAH, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3257-2015·2015-10-07

    KAL Amino Acid Complex Recalled for Undeclared Milk Allergen

    Nutraceutical International is recalling KAL Amino Acid Complex because the ingredient list does not explicitly state 'milk,' despite containing casein.

    Product
    KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16701·2015-10-07

    BRP Recalls Youth Can-Am ATVs Due to Fuel Filter Fire Hazard

    BRP is recalling about 240 Youth Model Can-Am DS 90 and DS 90X ATVs because a fuel filter defect can cause leaks and fire. No injuries have been reported.

    Product
    Youth Model Can-Am all-terrain vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2823-2015·2015-10-07

    Medtronic Solera Screwdrivers Recalled for Tip Deformation Risk

    Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.

    Product
    P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide