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.

36951–36975 of 73761

  • SevereNHTSA·18E092000·2018-09-20

    BMW Recalls TurboCord Portable Chargers Due to Fire and Shock Risk

    BMW is recalling TurboCord Portable Chargers because failing capacitors may cause electrical shock or fire, increasing the risk of injury or death.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V652000·2018-09-20

    BMW Recalls 2018-2019 Models for TurboCord Charger Fire Risk

    BMW is recalling specific 2018-2019 electric and hybrid models because capacitors in the TurboCord Portable Chargers may fail, posing a shock or fire hazard.

    Product
    BMW — BMW 740LE, 530E, X5, I3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E091000·2018-09-20

    Toyota Recalls Scion xB and tC Vehicles with TRD Brake Kits

    Toyota is recalling 2008-2015 Scion xB and 2011-2016 Scion tC vehicles equipped with specific TRD brake kits because the hoses may fail, increasing crash risk.

    Product
    SCION — SCION XB, TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18227·2018-09-20

    Kaz Recalls Stinger Insect Zappers Due to Internal Shock Hazard

    Kaz is recalling about 72,000 Stinger insect zappers because the internal kill grid can detach, posing a shock hazard. No injuries have been reported.

    Product
    Stinger Insect Zappers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18225·2018-09-20

    Weeplay Kids Recalls Children's Coveralls Due to Choking Hazard

    Weeplay Kids is recalling ED by Ellen DeGeneres children's coveralls because the bunny applique can detach, posing a choking hazard to young children.

    Product
    ED by Ellen DeGeneres coveralls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18767·2018-09-20

    Titan Recalls Weight Lifting Safety Straps Due to Injury Hazard

    Titan is recalling weight lifting safety straps because stitching can come loose, causing heavy weights to fall. No injuries have been reported.

    Product
    Titan safety straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1203-2018·2018-09-19

    FDA Recalls Respitrol Homeopathic Medicine Due to Microbial Contamination

    The FDA is recalling Respitrol Homeopathic OTC Medicine because it is contaminated with microorganisms, including Staphylococcus saprophyticus and Burkholderia cepacia.

    Product
    Respitrol, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-003-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·081-2018·2018-09-19

    Cargill Recalls Ground Beef Due to E. coli O26 Contamination

    Cargill Meat Solutions is recalling approximately 132,606 pounds of ground beef products that may be contaminated with E. coli O26. The recall follows an investigation linking the bacteria to 17 illnesses and one death.

    Product
    Cargill Meat Solutions — Cargill Meat Solutions Recalls Ground Beef Products due to Possible E. coli O26 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1200-2018·2018-09-19

    FDA Recalls Compulsin Homeopathic OTC Medicine Due to Microbial Contamination

    The FDA is recalling Compulsin Homeopathic OTC Medicine because it is contaminated with microorganisms, including Staphylococcus saprophyticus and Burkholderia cepacia.

    Product
    Compulsin, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-034-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1206-2018·2018-09-19

    Accord Recalls Hydrochlorothiazide Tablets Due to Product Mix-Up

    Accord Healthcare is recalling Hydrochlorothiazide 12.5 mg tablets because a customer complaint found Spironolactone 25 mg tablets in the bottles.

    Product
    HYDROCHLOROTHIAZIDE — HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1201-2018·2018-09-19

    FDA Recalls Neuroveen Homeopathic OTC Medicine for Microbial Contamination

    The FDA is recalling Neuroveen Homeopathic OTC Medicine due to microbial contamination with Staphylococcus saprophyticus and Burkholderia cepacia.

    Product
    Neuroveen, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-015-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1202-2018·2018-09-19

    HelloLife Recalls Thyroveev Homeopathic Medicine Due to Microbial Contamination

    HelloLife is recalling 370 bottles of Thyroveev homeopathic medicine due to microbial contamination. The product was distributed nationwide and internationally.

    Product
    Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-025-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V647000·2018-09-19

    Spartan Metrostar Emergency Vehicles Recalled for Wheel Stud Defect

    Spartan Motors is recalling 2018-2019 Metrostar emergency vehicles because improperly heat-treated wheel studs may fail, potentially causing the wheel to detach.

    Product
    SPARTAN — SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V646000·2018-09-19

    Freightliner Recalls 2018-2019 Models Due to Steering Shaft Defect

    Daimler Trucks North America is recalling 2018-2019 Freightliner 108SD, 114SD, and Business Class M2 vehicles because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.

    Product
    FREIGHTLINER — FREIGHTLINER 108SD, 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V643000·2018-09-19

    Livin' Lite CampLite Travel Trailers Recalled for Drawbar Crack Risk

    Livin' Lite is recalling 2017-2019 CampLite travel trailers because the drawbar may crack, causing the trailer to separate from the tow vehicle.

    Product
    LIVIN' LITE — LIVIN' LITE CAMPLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V641000·2018-09-19

    Daimler Trucks Recalls 2019 Freightliner and Western Star Trucks for Tire Defect

    Daimler Trucks is recalling 2019 Freightliner and Western Star trucks because exposed tire sidewall steel cords may cause rapid air loss, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4900, 4700, BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3025-2018·2018-09-19

    Intuitive Surgical Recalls da Vinci EndoWrist Scissors Due to Cracking Risk

    Intuitive Surgical is recalling 42,274 da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors because cracks may form in the extension tube, potentially causing fragments to fall into patients.

    Product
    da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. 470179-14 Product Usage: EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation of tissue, including: grasping, cutting, blunt…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3045-2018·2018-09-19

    Beaver Accu-Temp High Temperature Cautery Recalled for Sterility Risk

    Beaver Visitec is recalling 800 units of Accu-Temp High Temperature Cautery devices due to a potential loss of sterility caused by packaging defects.

    Product
    Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model Number 8445000 Product Usage: The indications and intended use of the High Temp cautery are for coagulating tissue or arresting bleeding from small vessels by heat conducted through the wire tip.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2995-2018·2018-09-19

    Ohio Medical Care-E-Vac 3 Portable Suction Pump Recall

    Ohio Medical is recalling 1,443 Care-E-Vac 3 portable suction pumps because a battery terminal may contact the pump, causing an electric short and loss of function.

    Product
    Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3024-2018·2018-09-19

    Intuitive Surgical Recalls da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors

    Intuitive Surgical is recalling 23,064 da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors because cracks in the extension tube may cause plastic fragments to fall into patients.

    Product
    da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation of tissue, including: grasping, cutting, blunt…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3021-2018·2018-09-19

    Cardiovascular Systems Recalls Orbital Atherectomy Saline Infusion Pumps

    Cardiovascular Systems Inc is recalling 18 Orbital Atherectomy System Saline Infusion Pumps because they may switch to stand-by during use, requiring a reset to continue treatment.

    Product
    CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000. Product Usage: Usage: The pump is a component of the OAS that provides the pumping mechanism and power to the OAD. The pump does not have an indication…
    Category
    Medical Device
    Distribution
    Distributed nationwide