The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44901–44925 of 73832

  • ModerateNHTSA·17V008000·2017-01-09

    Heartland Recalls 2017 Mallard Trailers for Incorrect Certification Label

    Heartland is recalling 2017 Mallard recreational trailers because the certification label may contain incorrect tire size or pressure information, which could lead to improper tire inflation or overloading.

    Product
    HEARTLAND — HEARTLAND MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-010717·2017-01-07

    Chicken Strips May Be Contaminated with Listeria, USDA Says

    USDA FSIS issued a public health alert about ready-to-eat chicken breast strips produced by House of Raeford on Sept. 29, 2016 that may be contaminated with Listeria monocytogenes. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert For Chicken Strips Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V004000·2017-01-06

    Fisker Karma Recall: Passenger Air Bag Inflators May Rupture in Crash

    Karma Automotive is recalling 2012 Fisker Karma vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    FISKER — FISKER KARMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V007000·2017-01-06

    Kia Recalls One 2016 Optima for Driver Air Bag Defect

    Kia is recalling one 2016 Optima because the driver's frontal air bag inflator seal may not be installed properly, potentially reducing inflation in a crash.

    Product
    KIA — KIA OPTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0819-2017·2017-01-04

    Cargill Recalls Wilbur Semi-Sweet Chocolate Drops for Undeclared Milk

    Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur Semi-Sweet Chocolate Drops because they may contain undeclared milk.

    Product
    Wilbur; IM10021; B558 Semisweet Chocolate Drops, 2000 CT; Net Weight 50 lb.; This item may contain dairy products; Cargill Cocoa & Chocolate, Inc., Lititz, PA 17543; BATCH 28116AANCB and 28116AANCC Material number: 100000081 packed in cardboard boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17063·2017-01-04

    Disney Recalls Infant Hoodies Due to Choking Hazard from Detaching Snaps

    Walt Disney Parks and Resorts is recalling Minnie and Mickey Mouse infant hoodie sweatshirts because the snaps can detach, posing a choking hazard to young children.

    Product
    Minnie and Mickey Mouse infant hoodie sweatshirts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0901-2017·2017-01-04

    Medtronic NIM EMG Endotracheal Tubes Recalled for Exposed Wire Hazard

    Medtronic Xomed is recalling NIM EMG Endotracheal Tubes because wire in the tubing can become exposed, posing potential harm to intubated patients.

    Product
    NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17064·2017-01-04

    Toshiba Laptop Battery Packs Recalled for Overheating and Fire Hazards

    Toshiba is expanding a recall of Panasonic lithium-ion battery packs for laptops due to overheating, burn, and fire risks. No injuries have been reported.

    Product
    Panasonic battery packs used in Toshiba laptop computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0906-2017·2017-01-04

    Bio-Botanica Recalls Vitamin D-3 Drops for Excess Dosage

    Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.

    Product
    Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0240-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Virt-Select Prenatal Softgels Due to GMP Deviations

    Virtus Pharmaceuticals is recalling Virt-Select Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert for cGMP deviations.

    Product
    Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-249-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0903-2017·2017-01-04

    Ortho-Clinical Diagnostics Recalls VITROS Intact PTH Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.

    Product
    VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Product Code 6802893 - Calibrators For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0241-2017·2017-01-04

    VirtPrex Prenatal Tablets Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling VirtPrex Prenatal/Postnatal Tablets because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-348-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0235-2017·2017-01-04

    Care-Tech Recalls Surgical Hand Scrub Due to Labeling and Cap Defects

    Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.

    Product
    Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0239-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Extra-Virt Plus DHA Prenatal Softgels

    Virtus Pharmaceuticals is recalling 2,406 bottles of Extra-Virt Plus DHA Prenatal/Postnatal Softgels because the API manufacturer is on FDA Import Alert.

    Product
    Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-251-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0238-2017·2017-01-04

    Virt-Advance Prenatal Softgels Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling Virt-Advance Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement, packaged in 90-count bottle, Rx only, Made in Canada, NDC 76439-357-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E001000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Rupture Recall

    Takata is recalling certain frontal passenger air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E002000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Module Recall

    Takata is recalling specific frontal passenger air bag inflators in 2012 vehicles registered in 14 states and territories due to a risk of rupture.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V002000·2017-01-03

    Audi Recalls 2012-2017 Models for Coolant Pump Fire Risk

    Volkswagen Group of America is recalling specific Audi models because a blocked coolant pump can overheat and cause a fire.

    Product
    AUDI — AUDI A4 ALLROAD, A6, Q5, A5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V001000·2017-01-03

    Audi Recalls 2011-2017 Q5 Vehicles Due to Side Air Bag Corrosion Risk

    Volkswagen Group of America is recalling 2011-2017 Audi Q5 vehicles because water in the sunroof drainage system may corrode side air bag inflators, posing a risk of serious injury.

    Product
    AUDI — AUDI Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V957000·2016-12-31

    Forest River Recalls 2017 Fifth-Wheel RVs Due to Door Hinge Defect

    Forest River is recalling 2017 XLR Toyhauler and Prime Time Spartan fifth-wheel vehicles because rear cargo door hinge welds may be insufficient, increasing the risk of personal injury.

    Product
    PRIME TIME — PRIME TIME, FOREST RIVER SPARTAN, XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V946000·2016-12-30

    Porsche Recalls 2017 Models Due to Side Air Bag Defect

    Porsche is recalling 2017 911, 718 Cayman, and 718 Boxster vehicles because the side air bag inflator initiator may fail to ignite during a crash.

    Product
    PORSCHE — PORSCHE 911, 718 CAYMAN, 718 BOXSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide