The Recall Desk

State

Northern Mariana Islands product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29501–29525 of 73621

  • HighCPSC·20099·2020-03-19

    Crate and Barrel Recalls Miles Glass Pitchers Due to Laceration Hazard

    Crate and Barrel is recalling Miles Glass Pitchers with Wood Lid because the handle can break, posing a laceration hazard. No injuries have been reported.

    Product
    Miles Glass Pitchers with Wood Lid
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20723·2020-03-19

    Plant Therapy Recalls Wintergreen Oils for Non-Child-Resistant Packaging

    Plant Therapy is recalling specific wintergreen essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Plant Therapy Wintergreen, Organic Wintergreen, Muscle Aid Synergy Blend, Tingly Mint Synergy Blend, and Vein Aid Synergy Blend Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V166000·2020-03-19

    BMW Recalls Motorcycles Due to Unclear Brake Fluid Reservoir Cap Labeling

    BMW is recalling specific 2018-2020 motorcycles because the brake fluid reservoir cap may not clearly state the required fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R NINE T RACER, R NINE T, R 1250 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E013000·2020-03-19

    BMW Recalls Motorcycle Brake Fluid Reservoir Caps for Labeling Defect

    BMW is recalling specific motorcycle brake fluid reservoir caps because they may not clearly state the required brake fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R 1250 R, R 1250 RS, R NINE T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20726·2020-03-19

    Kawasaki Recalls MULE PRO Utility Vehicles Due to Steering Shaft Wear

    Kawasaki is recalling approximately 80,000 MULE PRO off-highway utility vehicles because excessive steering shaft wear can affect steering control, posing a crash hazard.

    Product
    Kawasaki MULE PRO off-highway utility vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V154000·2020-03-18

    Bentley Recalls Bentayga Vehicles Due to Third-Row Seat Belt Defect

    Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1476-2020·2020-03-18

    Qiagen Rotor-Gene Q Software Recall for Incorrect Concentration Reporting

    Qiagen is recalling Rotor-Gene Q instruments with software version 2.3.4 because a bug causes concentration results to be reported as logarithmic values, potentially leading to false negative test results.

    Product
    QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time detection of PCR assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1003-2020·2020-03-18

    American Health Packaging Recalls Ranitidine Tablets Due to NDMA Levels

    American Health Packaging is recalling 53,619 cartons of Ranitidine Tablets, 150 mg, due to potential N-Nitrosodimethylamine (NDMA) amounts above FDA-established levels.

    Product
    Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC carton: 60687-322-01; NDC Unit Dose Card: 60687-322-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1004-2020·2020-03-18

    Precision Dose Recalls Ranitidine Oral Solution Due to NDMA Impurity

    Precision Dose Inc. is recalling Ranitidine Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit Dose Cups per case, NDC: 68094-204-61; Unit Dose Cup NDC: 68094-204-59], Rx only, Precision Dose, Inc., South Beloit, IL 61080
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1475-2020·2020-03-18

    Getinge 88-Series Washer Disinfectors Recalled for Chamber Leakage Risk

    Maquet Cardiovascular is recalling Getinge 88-Series washer disinfectors because ruptured spot welds may cause water leakage, posing slip and infection risks.

    Product
    Getinge 88-Series-washer disinfectors intended for cleaning, disinfection and drying Model Number: 88-5 Part Number: 88-103; 88-203
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1455-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Hypodermic Safety Needles

    Cardinal Health is recalling Monoject Hypodermic Safety Needles that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.

    Product
    Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V157000·2020-03-18

    Daimler Vans Recalls 2019 Sprinter Vehicles Due to Tire Installation Error

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because winter tires may be installed incorrectly, reducing traction in wet or snowy conditions.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 4500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V155000·2020-03-18

    Daimler Vans Recalls 2018-2019 Sprinter Vehicles for Incorrect Spare Tire Label

    Daimler Vans is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vehicles because the spare tire label may list the maximum speed in kilometers per hour instead of miles per hour.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1005-2020·2020-03-18

    Acetaminophen Tablets Recalled Due to Foreign Tablet Contamination

    H J Harkins Company Inc is recalling Acetaminophen 500 mg tablets because a foreign Women's Prenatal tablet was found in the product.

    Product
    Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC 52959-0002-30), b) 42-count bottles (NDC 52959-0002-42), c) 45-count bottles (NDC 52959-0002-45) and e) 50-count bottles (NDC 52959-0002-50) Repack: H.J. Harkins Co., Inc. Grover Beach, CA 93433
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1453-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Monoject Syringes with Safety Needles

    Cardinal Health is recalling Monoject 3mL syringes with safety needles because they were shipped as non-sterile despite labeling. The firm is not aware of any patient harm reports.

    Product
    Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20725·2020-03-18

    Earth Sonnets Recalls Wintergreen Essential Oil for Packaging Defect

    Earth Sonnets is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Earthsonnets Wintergreen (Gualtheria procumbens) Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V151000·2020-03-18

    Lamborghini Recalls 2020 Aventador SVJ Models for Door Handle Defect

    Lamborghini is recalling 26 2020 Aventador SVJ vehicles because the interior door handle mechanism may fail, preventing the door from opening from inside.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ COUPE, AVENTADOR SVJ ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V156000·2020-03-18

    Mercedes-Benz and Freightliner Sprinter Recalled for Missing Spare Tire Label

    Daimler Vans USA is recalling 2018-2019 Sprinter vans because the spare tire may lack a maximum speed label, increasing the risk of tire failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1473-2020·2020-03-18

    Medicrea Iliac Screws Recalled Due to Incorrect Component Orientation

    Medicrea International is recalling 3,529 Iliac Screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the shank.

    Product
    Iliac Screws, multiple sizes, Article Nos. B36020500 B36020570 B36020580 B36020590 B36027500 B36027570 B36027580 B36027590 B36028500 B36028570 B36028580 B36028590 B36029500 B36029570 B36029580 B36029590 Screws manufactured in titanium alloy Ti-6Al-4V LI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2020·2020-03-18

    Medtronic Simulus 850 Sizer Kits Recalled Due to Porcine Tissue Contact

    Medtronic is recalling six Simulus 850 Semi Rigid Ring/Band Accessory Kits because demonstration units may have contacted porcine tissue.

    Product
    Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to size a patient's mitral or tricuspid valve in cardiac procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide