The Recall Desk

State

Northern Mariana Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42501–42525 of 73829

  • ModerateFDA (Drugs)·D-0927-2017·2017-07-05

    Doxycycline Hyclate API Recalled for Misbranding Under FDA Import Alert

    American Pharmaceutical Ingredients LLC is recalling Doxycycline Hyclate USP active pharmaceutical ingredient due to misbranding. The product is subject to FDA Import Alert 66-66.

    Product
    Doxycycline Hyclate USP, active pharmaceutical ingredient, a) 25 g packaged in a 500 cc container (NDC: 58597-8082-4), b) 100 g packaged in 16 oz container (NDC: 58597-8082-6), c) 500 g packaged in a 2500 cc container (NDC: 58597-8082-7) and a 1,000 g packaged in 1 gallon…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2641-2017·2017-07-05

    Merge Healthcare Recalls Masimo SPO2 Sensors for Display Failure

    Merge Healthcare is recalling Masimo SPO2 ear clip sensors because cables may stop displaying SpO2 readings, causing slight delays in patient care.

    Product
    Masimo SPO2 Sensor, ear clip-adult (Merge Part Number: HW-HEMO-00047), Product Usage: Merge Hemodynamics monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure. The Monitoring System is for the monitoring of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2644-2017·2017-07-05

    Exactech Novation Calcar Planer Guide Tip Recalled for Labeling Clarification

    Exactech is recalling 477 Novation Calcar Planer Guide Tips to update labeling with a caution about instrument breakage.

    Product
    Exactech 1.5" Novation Calcar Planer Guide Tip To assist the surgeon in the implantation of Novation hip system components according to a conventional technique for total hip replacement. Specifically, these instruments are reusable, surgically invasive, and intended for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0924-2017·2017-07-05

    Apothecary by Design Recalls Progesterone Injection Vials Due to Closure Defect

    Apothecary by Design is recalling 25 vials of Progesterone Injection in Olive Oil due to a manufacturing defect where metal closures may adhere to rubber stoppers, potentially compromising container integrity.

    Product
    Progesterone Injection in Olive Oil With Benzyl Alcohol 10%, 50mg/mL, 10mL Multi-Dose Vial, Rx only, Apothecary by Design, 141 Preble Street, Portland, ME.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0926-2017·2017-07-05

    Gaviscon Chewable Tablets Recalled for High Magnesium Levels

    Sanofi-Aventis is recalling Gaviscon chewable tablets due to high out-of-specification magnesium levels. The recall covers 2,980 bottles distributed in the US, Puerto Rico, and the UK.

    Product
    Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0928-2017·2017-07-05

    BuPROPion HCL Tablets Recalled for Moisture Content Failures

    Mckesson Packaging Services is recalling BuPROPion HCL Tablets, 75 mg, due to out-of-specification moisture content.

    Product
    BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2650-2017·2017-07-05

    Medtest Liquid Creatine Kinase Reagent Set Recalled for Labeling Mismatch

    Medtest Holdings is recalling Pointe Scientific Liquid Creatine Kinase Reagent Sets because the product insert does not match the approved premarket notification.

    Product
    Pointe Scientific Liquid Creatine Kinase Reagent Set Device is a kit comprised of two reagents an R 1 Buffer and R2 CK enzyme solution. Intended Use: For the kinetic quantitative determination of creatine kinase activity in serum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V425000·2017-07-03

    Toyota Recalls Tacoma and 4Runner Vehicles with Detaching Hood Scoops

    Southeast Toyota Distributors is recalling 2011-2016 Toyota Tacoma and 4Runner vehicles because accessory hood scoops may detach, creating a road hazard.

    Product
    TOYOTA — TOYOTA TACOMA, 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V426000·2017-07-03

    Triumph Recalls 2017-2018 Street Cup Motorcycles for Wiring Defect

    Triumph is recalling 2017-2018 Street Cup motorcycles because the hazard light wiring harness may strain during steering, potentially causing the lights to fail and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH STREET CUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V424000·2017-06-30

    Acura Recalls 2017 MDX Sport Hybrid for Fuel Hose Misrouting

    Honda is recalling 2017 Acura MDX Sport Hybrid vehicles because fuel hoses may be misrouted, potentially causing a fuel leak and fire risk.

    Product
    ACURA — ACURA MDX SPORT HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V419000·2017-06-30

    KZRV Recalls 2018 Sportsmen LE Trailers Due to Improper Spare Tires

    KZRV is recalling 2018 Sportsmen LE recreational trailers because they were supplied with spare tires of incorrect size and load capacity, which may fail if used while fully loaded.

    Product
    KZRV — KZRV SPORTSMEN LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V422000·2017-06-30

    Jayco Recalls 2017 Hummingbird Travel Trailers Due to Incorrect Tire Labels

    Jayco is recalling 2017 Hummingbird travel trailers because tire labels list incorrect pressure requirements, which could lead to tire failure and crashes.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER HUMMINGBIRD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V413000·2017-06-29

    Newmar Recalls 2018 Motorhomes Due to Fuel Pump Drive Gear Slip Risk

    Newmar is recalling 2018 London Aire, King Aire, and Essex motorhomes because a fuel pump drive gear could slip, causing an engine stall and increasing crash risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE, KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V412000·2017-06-29

    GM Recalls 2016-2017 Buick Envision for Headliner Safety Defect

    General Motors is recalling 2016-2017 Buick Envision vehicles because replacement headliners may lack required impact-absorbing foam, increasing injury risk in crashes.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V415000·2017-06-29

    Lexus Recalls 2017 ES350 Vehicles Due to Steering Tie Rod Defect

    Toyota is recalling 2017 Lexus ES350 vehicles because the right-hand tie rod lock nut may loosen, potentially causing loss of steering and increasing crash risk.

    Product
    LEXUS — LEXUS ES350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V429000·2017-06-29

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Mazda is recalling 2007-2011 CX-7, CX-9, and 2009-2011 Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V417000·2017-06-29

    Honda Recalls 2007-2011 CR-V Vehicles for Air Bag Inflator Defect

    Honda is recalling 2007-2011 CR-V vehicles where the passenger air bag inflator may have an incorrect wire harness, potentially preventing deployment in a crash.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide