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.

44301–44325 of 73832

  • HighNHTSA·17V121000·2017-02-27

    Tiffin Recalls 2012 Phaeton Motorhomes Due to Exhaust Fire Risk

    Tiffin is recalling 35 model-year 2012 Phaeton motorhomes because the exhaust pipe is mounted too close to the floor, creating a fire hazard.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V117000·2017-02-24

    Forest River Recalls 2017 Sandstorm and Stealth RVs for Propane Leak Risk

    Forest River is recalling 2017 Sandstorm and Stealth recreational vehicles because the liquid propane line may be damaged by the axle, creating a fire or explosion hazard.

    Product
    FOREST RIVER — FOREST RIVER SANDSTORM, STEALTH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V118000·2017-02-24

    Forest River Recalls 2017 Wildwood and Salem Trailers Due to Propane Leak Risk

    Forest River is recalling 2017 Wildwood and Salem recreational trailers because an improperly installed refrigerator vent allows propane gas to enter the vehicle, increasing the risk of fire or explosion.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17096·2017-02-23

    Little Tikes Recalls Toddler Swings Due to Fall Hazard

    Little Tikes is recalling about 540,000 2-in-1 Snug 'n Secure Pink toddler swings because the plastic seat can crack or break, posing a fall hazard.

    Product
    Little Tikes™ 2-in-1 Snug 'n Secure Pink toddler swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·17094·2017-02-23

    Carrier Recalls Packaged Terminal Air Conditioners and Heat Pumps Due to Fire Hazard

    Carrier is expanding a recall for about 94,000 packaged terminal air conditioners and heat pumps because the power cord plug can overheat, posing a fire hazard.

    Product
    Packaged Terminal Air Conditioners (PTAC) and Packaged Terminal Heat Pumps (PTHP)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V116000·2017-02-23

    GM Recalls 2017 Buick LaCrosse for Power Steering Seal Defect

    General Motors is recalling 2017 Buick LaCrosse vehicles because water may enter the electric power steering connectors, potentially causing a loss of power steering.

    Product
    BUICK — BUICK LACROSSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V115000·2017-02-23

    BMW and Rolls-Royce Recall Vehicles for Air Bag Initiator Defect

    BMW is recalling 2017 430i, 440i, M4, and Rolls-Royce Dawn vehicles because seat-mounted air bag inflator initiators may fail to ignite during a crash.

    Product
    BMW — BMW, ROLLS-ROYCE 430I, 440I, M4, DAWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17095·2017-02-23

    STIHL Recalls Gas-Powered Chain Saws Due to Fire and Burn Hazards

    STIHL is recalling about 100,000 gas-powered chain saws because a leaking fuel line can cause fire and burn hazards. Consumers should stop using the saws and return them for a free repair.

    Product
    STIHL gas-powered chain saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·015-2017·2017-02-22

    Ready Pac Foods Recalls Chicken Salad Due to Possible Listeria Contamination

    Ready Pac Foods is recalling approximately 59,225 pounds of Puro Picante Blazin Hot chicken salad due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Ready Pac Produce, Inc. — Ready Pac Foods Inc. Recalls Chicken Salad Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1188-2017·2017-02-22

    GE Healthcare Recalls Discovery MR450 MRI Scanners Due to Burn Risk

    GE Healthcare is recalling 60 Discovery MR450 MRI scanners because a component failure can cause the patient bore to heat up, potentially leading to serious burns.

    Product
    Discovery MR450 The systems are whole body magnetic resonance scanners designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1192-2017·2017-02-22

    Integra Cadence Total Ankle System Recalled Due to Tibial Fractures

    Integra LifeSciences Corp. is recalling 944 units of the Cadence Total Ankle System because posterior tibial fractures have been reported.

    Product
    Integra Cadence Total Ankle System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1123-2017·2017-02-22

    Physio-Control Recalls LIFEPAK 15 Defibrillators Due to Relay Failure

    Physio-Control is recalling 338 LIFEPAK 15 defibrillators because an internal relay may fail, preventing the device from delivering defibrillation energy.

    Product
    LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1193-2017·2017-02-22

    Stryker Restoris RIO Reamer Handle Recalled for Engagement Failure

    Mako Surgical Corporation is recalling 595 Stryker Restoris RIO Reamer Handles because they may fail to engage mating components during surgery.

    Product
    Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components during acetabular reaming in MAKO Total Hip procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1103-2017·2017-02-22

    Zimmer Biomet Recalls Reverse Shoulder Humeral Trays Due to Fracture Risk

    Zimmer Biomet is recalling 4,388 Comprehensive Reverse Shoulder System Humeral Trays because they are fracturing at higher-than-anticipated rates, posing a risk of revision surgery.

    Product
    Comprehensive Reverse Shoulder System Humeral Tray Model 115340
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1194-2017·2017-02-22

    Argon Medical Devices Recalls Bone Marrow Aspiration Needles Due to Sterility Risk

    Argon Medical Devices is recalling specific bone marrow aspiration needles because a potential defect in the blister packaging may compromise the sterility of the product.

    Product
    BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX Intended for the purpose of harvesting bone and/or bone marrow specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1218-2017·2017-02-22

    Aesculap GN200 Caiman HF Generators Recalled for Faulty Component

    Aesculap Implant Systems LLC is recalling 24 GN200 Caiman HF generators due to a faulty component that may impact proper device functioning.

    Product
    GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2017·2017-02-22

    Atrium Medical Recalls Maquet Ocean Water Seal Chest Drains

    Atrium Medical Corporation is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after use.

    Product
    Maquet Ocean Water Seal Chest Drain, Single Collection w/AC Reference: 2002-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1210-2017·2017-02-22

    Atrium Medical Recalls Maquet Express Dry Seal Suction OCEAN DRAIN Chest Drains

    Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction OCEAN DRAIN chest drains because the manual vent valve may fail to re-seal after use.

    Product
    Maquet Express Dry Seal Suction OCEAN DRAIN, SINGLE Reference: 2002-400 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1191-2017·2017-02-22

    Encore Medical Recalls LIMA Modular Revision Hip Stems Due to Sterilization Error

    Encore Medical is recalling 13 LIMA Modular Revision Hip Stems because they were inadvertently re-sterilized, which may compromise the integrity of the safety screw.

    Product
    LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral hip stem is made up of a modular stem coupled with a proper neck by means of a Morse taper stabilized during the implantation phase by a safety screw. This system is particularly…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17093·2017-02-22

    Moose Toys Recalls Little Live Pets Lil Frog Toys Due to Battery Hazards

    Moose Toys is recalling Little Live Pets Lil Frog toys because the battery cap can become a projectile and chemicals can leak, causing eye irritation.

    Product
    Little Live Pets Lil Frog and Lil Frog Lily Pad toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1195-2017·2017-02-22

    Argon Medical Devices Recalls T-LOK Bone Marrow Biopsy Needles

    Argon Medical Devices is recalling T-LOK bone marrow biopsy needles due to a potential defect in the blister packaging that may compromise sterility.

    Product
    T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN; T-LOK BONE MARROW BIOPSY NEEDLE 11G x 4 EXT CAN Intended for the purpose of harvesting bone and/or bone marrow specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide