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.

36826–36850 of 73761

  • HighFDA (Devices)·Z-3224-2018·2018-10-03

    Philips Allura Xper FD2O Biplane Recall for Monitor Suspension Detachment Risk

    Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    Allura Xper FD2O Biplane, System Code 722008 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3216-2018·2018-10-03

    Philips INTEGRIS Allura Monitor Ceiling Suspension Recall for Detachment Risk

    Philips is recalling INTEGRIS Allura 15-12 systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.

    Product
    INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1213-2018·2018-10-03

    Hetero Recalls Montelukast Sodium Tablets Due to Blue Specks

    Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because a pharmacist reported blue specks on the tablets.

    Product
    MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3250-2018·2018-10-03

    Zimmer Biomet Recalls Vanguard 360 Knee Augments Due to Missing Bolt

    Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained one bolt instead of the required two.

    Product
    Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1215-2018·2018-10-03

    Baxter Recalls Levofloxacin Injection Bags Due to High Potency

    Baxter Healthcare is recalling 523,896 bags of Levofloxacin Injection in 5% Dextrose because the drug concentration was higher than specified.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3244-2018·2018-10-03

    Tosoh G8 Automated HPLC Analyzer Recalled for Missing 510(k) Software

    Tosoh Bioscience Inc is recalling eight G8 Automated HPLC Analyzers because they were distributed with software that lacks a 510(k).

    Product
    G8 Automated HPLC Analyzer - 723G8 Product Usage - In vitro diagnostic use for the quantitative measurement of % hemoglobin A1c in whole blood specimens. This test is to be used as an aid in the diagnosis of diabetes and as an aid in identifying patients who may be at risk…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1207-2018·2018-10-03

    Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect

    Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.

    Product
    MINIVELLE — MINIVELLE (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1210-2018·2018-10-03

    Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defects

    Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.

    Product
    MINIVELLE — MINIVELLE (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3249-2018·2018-10-03

    Zimmer Biomet Recalls Vanguard 360 Knee Augments Due to Missing Bolt

    Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained only one bolt instead of the required two.

    Product
    Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 Intended for use in Total Knee Arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1208-2018·2018-10-03

    Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect

    Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.

    Product
    MINIVELLE — MINIVELLE (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1988-2018·2018-10-03

    Caffeine-Free Barq's Root Beer Recalled for Mislabeling

    Swire Coca Cola USA is recalling Caffeine-Free Barq's Root Beer 12 Packs due to mislabeling. The recall covers 2,945 cases distributed nationwide.

    Product
    Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18V687000·2018-10-02

    Entegra Recalls 2019 Motorhomes Due to Park Brake Defect

    Entegra is recalling 2019 Aspire, Anthem, and Insignia motorhomes because the park brake may fail to hold the vehicle on a grade.

    Product
    ENTEGRA — ENTEGRA INSIGNIA, ASPIRE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V689000·2018-10-02

    Jayco Recalls 2019 Precept Motorhomes Due to Wheel Stud Defect

    Jayco is recalling 2019 Precept and Precept Prestige motorhomes because improperly heat-treated front wheel studs may break, increasing crash risk.

    Product
    JAYCO — JAYCO PRECEPT, PRECEPT PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V688000·2018-10-02

    Entegra Recalls 2019 Motorhomes Due to Door Latch Adjustment Issue

    Entegra is recalling 2019 Anthem, Aspire, Cornerstone, and Insignia motorhomes because improperly adjusted entry door latch rods may allow the door to open during transit.

    Product
    ENTEGRA — ENTEGRA ASPIRE, ANTHEM, CORNERSTONE, INSIGNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V686000·2018-10-02

    Jayco Recalls 2019 Jay Flight Trailers Due to Wiring Defect

    Jayco is recalling 2019 Jay Flight travel trailers because incorrectly wired turn signal and brake lights may fail to operate, increasing crash risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V682000·2018-10-01

    Winnebago Recalls Minnie Drop Trailers Due to Propane Line Fire Risk

    Winnebago is recalling 2017-2019 Minnie Drop trailers because a missing clamp may allow the propane line to contact the refrigerator burner, posing a fire risk.

    Product
    WINNEBAGO — WINNEBAGO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V680000·2018-09-28

    BMW Recalls 2019 X6 and X6 M for Rear Suspension Defect

    BMW is recalling 2019 X6 and X6 M vehicles because improperly hardened rear suspension bolts may break, increasing crash risk.

    Product
    BMW — BMW X6, X6 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V681000·2018-09-28

    KZRV Sonic Travel Trailer Recall for Propane Manifold Fire Risk

    KZRV is recalling 2017-2019 Sonic 190VRB travel trailers because the liquid propane manifold may be located close to the axle tube, posing a fire risk.

    Product
    KZRV — KZRV SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18234·2018-09-28

    Boy Story Recalls Mason and Billy Action Dolls Due to Choking Hazard

    Boy Story is recalling Mason and Billy action dolls because the vinyl joints can break, creating pieces that pose a choking hazard to young children.

    Product
    Mason & Billy action dolls and Mason & Billy HeForShe special edition action dolls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V662000·2018-09-27

    Honda Recalls 2010-2014 Vehicles for Air Bag Inflator Explosion Risk

    Honda is recalling 2010-2014 Ridgeline, Element, and Acura RL vehicles because the passenger air bag inflator may explode, posing a risk of serious injury or death.

    Product
    HONDA — HONDA, ACURA RIDGELINE, RL, ELEMENT
    Category
    Vehicle
    Distribution
    Distributed nationwide