The Recall Desk

State

Northern Mariana Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36326–36350 of 73760

  • SevereNHTSA·18V757000·2018-10-26

    Altec Recalls 2018 Digger Derricks and Aerial Devices for Fastener Failure

    Altec is recalling 2018 Digger Derricks and Aerial Devices because high-strength fasteners may fail, causing the pedestal to separate from the turn table and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·105-2018·2018-10-26

    Suzanna's Kitchen Recalls Grilled Chicken Strips Due to Unapproved Thallium

    Suzanna's Kitchen is recalling approximately 15,408 pounds of grilled chicken breast strips because they contain unapproved concentrations of thallium. No illnesses have been reported.

    Product
    Suzanna's Kitchen Inc. — Suzanna's Kitchen, Inc., Recalls Poultry Products due to an Unapproved Substance
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18V758000·2018-10-26

    Isuzu and Chevrolet Trucks Recalled for Cab Tilt-Lock Warning Defect

    Isuzu is recalling 2018-2019 Chevrolet Low Cab Forward 6500 and Isuzu FTR trucks because the cab tilt-lock may not provide an adequate warning after servicing.

    Product
    ISUZU — ISUZU, CHEVROLET FTR, LOW CAB FORWARD 6500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V756000·2018-10-26

    Pierce Fire Trucks Recalled for Whelen Brake Light Wiring Defect

    Pierce is recalling 2017-2018 vehicles equipped with Whelen accessory brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    PIERCE — PIERCE SABER, VELOCITY, ARROW XT, ENFORCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V755000·2018-10-25

    BMW Recalls Diesel Vehicles Due to EGR Cooler Leak Fire Risk

    BMW is recalling specific 2013-2018 diesel models because a leaking EGR cooler can cause the intake manifold to melt, increasing the risk of a fire.

    Product
    BMW — BMW 328D, X5, 535D, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V754000·2018-10-25

    Kia Recalls 2018 Stinger Vehicles Due to Wiring Fire Risk

    Kia is recalling 2018 Stinger vehicles because a front wiring harness may be damaged by a burr, increasing the risk of a fire.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19015·2018-10-25

    Haier Top-Mount Refrigerators Recalled Due to Fire Hazard

    Haier America is recalling about 137,000 top-mount refrigerators because an electrical component can short circuit, posing a fire hazard.

    Product
    Haier Top-Mount Refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V753000·2018-10-25

    Toyota Recalls 4Runners With Incorrect Weight Rating Labels

    Southeast Toyota Distributors is recalling 2017-2019 Toyota 4Runners with TRD wheel packages because incorrect weight labels may lead to vehicle overloading.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V752000·2018-10-25

    Forest River Cherokee Recalled for Insufficient Awning Fasteners

    Forest River is recalling 2018-2019 Cherokee Alpha Wolf and 2019 Arctic Wolf trailers because awning fasteners may be insufficient, risking arm detachment.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19023·2018-10-25

    CB2 Recalls Pendant Lights Due to Fire and Shock Hazards

    CB2 is recalling Colby pendant lights because loose electrical wiring insulation poses fire and shock risks. No injuries have been reported.

    Product
    Pendant lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19019·2018-10-25

    Pacific Cycle Recalls Schwinn Abbott Mountain Bicycles Due to Fall Hazard

    Pacific Cycle is recalling 2018 Schwinn Abbott mountain bicycles because the downtube can crack, posing a fall hazard. One injury involving cuts and abrasions has been reported.

    Product
    2018 Schwinn Abbott Adult Men's Full Suspension Mountain Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19021·2018-10-25

    Shimano Recalls Lazer Bicycle Helmets Due to Head Injury Risk

    Shimano is recalling specific Lazer bicycle helmet models because they do not comply with federal safety standards, posing a risk of head injury.

    Product
    Lazer bicycle helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·104-2018·2018-10-25

    All Peoples Food Recalls Smoked Whole Chicken for Undeclared MSG

    All Peoples Food is recalling approximately 3,904 pounds of smoked whole chicken products because they contain monosodium glutamate (MSG) that is not declared on the label.

    Product
    Recall Notification Report 104-2018 (Smoked Whole Chicken Products)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0074-2019·2018-10-24

    CVS Sinus Relief Nasal Spray Recalled for Pseudomonas Contamination

    Product Quest Manufacturing LLC is recalling CVS-branded Sinus Relief nasal spray due to failed microbiological testing for Pseudomonas aeruginosa.

    Product
    Sinus Relief (oxymetazoline HCl) Nasal decongestant, 0.05%, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 43236 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0071-2019·2018-10-24

    CeraVe Healing Lip Balm Recalled for Staphylococcus Aureus Contamination

    Product Quest Manufacturing LLC is recalling CeraVe Healing Lip Balm/SPF 30 due to failed microbiological testing for Staphylococcus aureus.

    Product
    CeraVe Healing Lip Balm/SPF 30 (avobenzone 3%, dimethicone 1%, homosalate 10%, octisalate 5%, octocrylene 10%, Net Wt. 0.15 oz. (4.25 g) stick, CeraVe LLC., New York, NY 10001, UPC 3 01872 49201 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0039-2019·2018-10-24

    Harmon Face Values Saline Nasal Gel Recalled for Quality Deviations

    Product Quest Manufacturing LLC is recalling Harmon Face Values Saline Nasal Gel with Soothing Aloe due to manufacturing deviations that could impact product quality.

    Product
    Harmon Face Values, Saline Nasal Gel with Soothing Aloe, 0.5 oz. (14.1 g) tube, Distributed by: Harmon Stores, Inc., Union, NJ 07083 USA, UPC 7 27510 00474 7 .
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0027-2019·2018-10-24

    Dermatone Sunscreen Stick Recalled for Staphylococcus Aureus Contamination

    Product Quest Manufacturing LLC is recalling Dermatone No-Touch Sunscreen Sticks because samples tested positive for Staphylococcus aureus.

    Product
    DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Distributed by: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 0 20908 05100 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0062-2019·2018-10-24

    Product Quest Recalls Well at Walgreens Sinus Relief Mist for Quality Issues

    Product Quest Manufacturing LLC is recalling Well at Walgreens ULTRA FINE Sinus Relief Mist due to manufacturing deviations that could impact product quality.

    Product
    Well at Walgreens, ULTRA FINE Sinus Relief Mist (Oxymetazoline HCl 0.05%) bottle, Sinus Reliever, Nasal Decongestant, 12 Hour Pump Mist, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7000-01, UPC 3 11917 18535 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0066-2019·2018-10-24

    Freeze It Spray Recalled for High Camphor Levels

    Product Quest Manufacturing LLC is recalling Freeze It spray cans due to high out-of-specification camphor levels.

    Product
    FREEZE IT (camphor 0.2% and menthol 3.5%) spray, 118.29 mL (4 fl. oz.) can, Distributed by: Expedite Products, Inc., Tampa, FL 33619 USA, UPC 8 56569 00203 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0063-2019·2018-10-24

    Walgreens Anefrin Nasal Spray Recalled for Manufacturing Quality Issues

    Product Quest Manufacturing LLC is recalling 355,056 bottles of Walgreens Anefrin Nasal Spray due to manufacturing conditions that could impact product quality.

    Product
    Walgreens, NO DRIP, Anefrin Nasal Spray (Oxymetazoline HCl 0.05%), Nasal Decongestant, Original, 12 Hour, Maximum Strength, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015,NDC 0363-7005-01, UPC 3 11917 18537 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0181-2019·2018-10-24

    OriGen Biomedical Recalls Reinforced Dual Lumen Cannulas Due to Deficiencies

    OriGen Biomedical is recalling 435 Reinforced Dual Lumen Cannulas because they may lack barium sulfate and have tips shorter than labeled.

    Product
    Reinforced Dual Lumen Cannula, 19Fr., REF: VV19F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support…
    Category
    Medical Device
    Distribution
    Distributed nationwide