The Recall Desk

State

Northern Mariana Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28851–28875 of 73619

  • ModerateFDA (Drugs)·D-1282-2020·2020-05-27

    West-Ward Recalls Ethacrynic Acid Tablets for Impurity Failures

    West-Ward Columbus Inc is recalling Ethacrynic Acid Tablets USP, 25 mg, because the product failed impurity and degradation specifications.

    Product
    Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·20127·2020-05-27

    Primark Recalls Kitten Heel Court Shoes Due to Chromium Levels

    Primark is recalling Wide Fit Kitten Heel Court Pumps because the leather insoles contain elevated levels of Chromium VI, posing a risk of skin irritation.

    Product
    Wide Fit Kitten Heel Court Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2064-2020·2020-05-27

    Philips HeartStart MRx Processor Board Replacement Kits Recalled for Damaged Bags

    Philips is recalling HeartStart MRx Processor Board PCA Replacement Kits because damaged ESD bags were used for storing components.

    Product
    HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx Monitorl/Defibrillator - Product Usage: is intended for use in hospital and prehospital settings by qualified medical personnel trained in the operation of the device and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2045-2020·2020-05-27

    Boston Scientific Recalls AMS 700 Reservoirs Due to Labeling Error

    Boston Scientific is recalling five AMS 700 100 mL Spherical Reservoirs with InhibiZone because they were incorrectly labeled as a different model.

    Product
    AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the treatment of chronic, organic, male erectile dysfunction (impotence).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2067-2020·2020-05-27

    DFINE Vertebral Hydraulic Assemblies Recalled for Incorrect Expiration Dates

    Merit Medical Systems is recalling 228 DFINE Vertebral Hydraulic Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.

    Product
    DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 1402 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological fractures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2073-2020·2020-05-27

    Capso Vision Recalls CapsoCam Plus Capsule Endoscopy Systems Due to Labeling Errors

    Capso Vision, Inc. is recalling 44 CapsoCam Plus video capsule systems because incorrect serial number labels may lead to patient misdiagnosis.

    Product
    CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2068-2020·2020-05-27

    Merit Medical Recalls DFINE Vertebral Assemblies Due to Incorrect Expiration Dates

    Merit Medical Systems is recalling 63 DFINE Vertebral Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.

    Product
    DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 3427 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1271-2020·2020-05-27

    Mylan Recalls Aloprim Injection Vials Due to Discoloration

    Mylan Institutional LLC is recalling 3,010 vials of Aloprim (allopurinol sodium) for Injection due to out-of-specification appearance and color results.

    Product
    ALOPRIM — ALOPRIM (ALLOPURINOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1272-2020·2020-05-27

    InvaGen Recalls Gabapentin Tablets Due to Impurity Test Failure

    InvaGen Pharmaceuticals is recalling 2,202 bottles of Gabapentin 600 mg tablets because they failed an impurity test during stability testing.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2038-2020·2020-05-27

    Pega Medical Recalls SLIM System Handle Due to Lot Number Mismatch

    Pega Medical Inc. is recalling three units of the SLIM System handle because the lot number on the instrument does not match the packaging label.

    Product
    Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V301000·2020-05-26

    Altec Recalls Aerial Devices With Incorrect Tow Hitch Load Ratings

    Altec is recalling 2014-2020 Aerial Devices with Class 3 towing hitches that may have incorrect load ratings or damage from overloading, increasing crash risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V302000·2020-05-26

    2020-2021 Keystone Cougar travel trailer cooktop fire hazard

    Keystone is recalling 2020-2021 Cougar travel trailers because the cooktop may not be properly sealed from the furnace, causing burner flames to invert and increasing fire risk. Dealers will inspect and seal it free of charge.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V300000·2020-05-23

    AEV TraumaHawk Ambulances Recalled for Rear Brake Line Wear Risk

    Halcore Group is recalling 2019-2020 AEV TraumaHawk ambulances because rear brake lines may wear from contact with suspension parts, risking brake loss.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2020-EXP ·2020-05-22

    Conagra Recalls Frozen Chicken and Turkey Bowls Due to Rock Contamination

    Conagra Brands is recalling approximately 276,872 pounds of frozen Healthy Choice Power Bowls because they may contain small rocks. No illnesses have been reported.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V298000·2020-05-22

    Mercedes-Benz Recalls 2012 C-Class Vehicles for Incorrect Air Bag Replacement

    Mercedes-Benz is recalling 2012 C-Class vehicles where an incorrect front passenger air bag may have been installed during a prior recall, potentially reducing crash protection.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG C63, C250, C300, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V297000·2020-05-22

    2020-2021 Forest River Surveyor Travel Trailers Safety Chain Recall

    Forest River is recalling 2020-2021 Surveyor travel trailers because the safety chains are insufficient for the trailer's weight rating and may break if the trailer becomes unhitched, risking complete detachment.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V299000·2020-05-22

    Triple E Recalls 2020 Unity Travel Trailers Due to Latch Defect

    Triple E is recalling 2020 Unity travel trailers because a latch may lock, blocking access to the propane shutoff valve and increasing fire risk.

    Product
    TRIPLE E — TRIPLE E UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V294000·2020-05-21

    Dennis Eagle Elite Garbage Trucks Recalled for Braking System Defect

    Dennis Eagle is recalling 2017-2018 Elite garbage trucks because the anti-lock braking system may activate on the wrong side, increasing stopping distance.

    Product
    DENNIS EAGLE — DENNIS EAGLE ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V295000·2020-05-21

    2021 Chevrolet Trailblazer lacks tire size and pressure label information

    General Motors is recalling certain 2021 Chevrolet Trailblazer vehicles with optional sport terrain tires because their certification labels do not show tire size and cold tire pressure information required by federal safety standards.

    Product
    CHEVROLET — CHEVROLET TRAILBLAZER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20746·2020-05-21

    Viva Doria Recalls Wintergreen Essential Oil Due to Packaging Defect

    Viva Doria is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    Viva Doria Wintergreen Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20747·2020-05-21

    Herman Miller and Design Within Reach Recall Dressers and Cabinets for Tip-Over Hazards

    Herman Miller and Design Within Reach are recalling Nelson and Lauki dressers and cabinets because they can tip over and entrap children. Consumers should stop using unanchored units and contact the company for a refund.

    Product
    Nelson and Lauki Dressers and Cabinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V286000·2020-05-20

    Toyota Recalls 2019-2020 RAV4 Models for Front Suspension Arm Cracks

    Toyota is recalling 2019-2020 RAV4 and RAV4 Hybrid vehicles because front lower suspension arms may crack and separate, risking loss of vehicle control.

    Product
    TOYOTA — TOYOTA RAV4, RAV4 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1932-2020·2020-05-20

    Philips Zenition 50 Medical Device Recalled for Electrical Contact Failure

    Philips is recalling 25 Zenition 50 devices because strain relief loss can cause electrical contacts to break, potentially exposing live parts or losing the video signal.

    Product
    Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V293000·2020-05-20

    Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect

    Vac-Tron is recalling 2016-2020 vacuum excavator trailers because the rear extends too far, failing federal safety standards and increasing crash risks.

    Product
    VAC-TRON — VAC-TRON CS 1270 GT, CS 870 GT, CS 873 GT, CV 1273 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide