The Recall Desk

State

Northern Mariana Islands product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22826–22850 of 73501

  • SevereNHTSA·21E094000·2021-11-12

    Chrysler Recalls Mopar High Pressure Fuel Pumps and 6.7L Engines

    Chrysler is recalling specific Mopar High Pressure Fuel Pumps and 6.7L Cummins Turbo Diesel Engines because the pump may fail, causing the engine to stall without warning.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22707·2021-11-12

    RH Lambeth Outdoor Metal Torches Recalled for Fire Hazard

    RH is recalling about 1,200 Lambeth outdoor metal torches because fuel can leak from the canister top and ignite, creating a fire hazard. No injuries have been reported. Consumers should stop using the torches and contact RH for a refund.

    Product
    Lambeth Outdoor Metal Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V879000·2021-11-12

    Fiat Recalls 2019 124 Spider Vehicles for Fuel Pump Defect

    Chrysler is recalling 2019 Fiat 124 Spider vehicles because a deformed fuel pump impeller may cause engine stalls, increasing crash risk.

    Product
    FIAT — FIAT 124 SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V875000·2021-11-12

    Mazda Recalls 2018-2020 Models for Fuel Pump Failure Risk

    Mazda is recalling 121,038 vehicles from 2018-2020 because a fuel pump impeller may crack, causing engine stalls and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA2, CX-9, MX-5, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V877000·2021-11-12

    2021-2022 Forest River Cherokee Travel Trailers Recalled for Incorrect Tire Placard

    Forest River is recalling 2021-2022 Cherokee travel trailers because the tire size and weight rating printed on the Federal Placard are incorrect. This could cause the vehicle to be overloaded and lose control.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22709·2021-11-12

    Hanna Andersson Baby Long Sleeve Wiggle Sets Recalled for Choking Hazard

    Hanna Andersson is recalling about 4,400 Baby Long Sleeve Wiggle Sets because snaps on the long sleeve top can detach, creating a choking hazard for young children. Consumers should stop using the product immediately and contact Hanna Andersson for a full refund.

    Product
    Baby Long Sleeve Wiggle Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22710·2021-11-12

    Hanna Andersson Baby Ruffle Rompers Recalled for Choking Hazard

    Hanna Andersson is recalling about 3,200 Baby Ruffle Rompers because metal snaps on the garment can detach, posing a choking hazard to infants and young children. The company is offering a full refund.

    Product
    Baby Ruffle Rompers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22708·2021-11-12

    VidaXL Steel Pool Ladders Recalled for Fall and Drowning Hazards

    VidaXL is recalling approximately 3,200 steel pool ladders because the steps can loosen during use, creating a risk of falls and drowning. Four fall incidents have been reported with no injuries.

    Product
    VidaXL Steel Pool Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·042-2021·2021-11-10

    Citterio Salame Sticks Recalled for Possible Salmonella Contamination

    Euro Foods is recalling Citterio salame sticks due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    Euro Food, Inc., DBA Citterio USA Corporation — Euro Foods Dba Citterio USA Corp. Recalls Salame Stick Products Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V873000·2021-11-10

    Jeep Wagoneer and Grand Cherokee Airbag Control Software Defect

    The Occupant Restraint Controller software in certain 2021-2022 Jeep models may be faulty, allowing airbags to disable without warning. This increases crash injury risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND WAGONEER, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0093-2022·2021-11-10

    Cubicin daptomycin injection recalled for glass particle contamination

    Merck Sharp & Dohme Corp. is recalling Cubicin (daptomycin for injection) 500 mg vials due to the presence of glass particles. The recall affects a single lot distributed nationwide.

    Product
    Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·043-2021·2021-11-10

    Innovative Solutions Recalls Chicken Patties Due to Possible Bone Contamination

    Innovative Solutions, Inc. is recalling raw chicken patty products that may contain pieces of bone. No illnesses have been reported.

    Product
    Innovative Solutions, Inc — Innovative Solutions, Inc. Recalls Chicken Patty Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0194-2022·2021-11-10

    IPL Coupling Gel and EcoGel 200 Recalled for Bacterial Contamination

    Lumenis, Inc. is recalling IPL Coupling Gel and EcoGel 200 due to potential bacterial contamination. Approximately 11,064 units were distributed worldwide.

    Product
    IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL Coupling Gel or EcoGel 200, 0.25 L (AX1009012) manufactured by Eco-Med Pharmaceutical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0089-2022·2021-11-10

    Irbesartan and Hydrochlorothiazide Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets 150/12.5 mg due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient, which resulted from CGMP deviations.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0087-2022·2021-11-10

    Irbesartan Tablets Recalled for Impurity in Active Ingredient

    Lupin Pharmaceuticals is recalling Irbesartan tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects 30-count and 90-count bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0092-2022·2021-11-10

    Methocarbamol Tablets Mislabeled with Incorrect Strength

    Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.

    Product
    Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0090-2022·2021-11-10

    Lupin Pharmaceuticals Irbesartan/Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets USP (300/12.5 mg) in 30-count and 90-count bottles due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V872000·2021-11-10

    Maserati Vehicles Recall: Fuel Line Sensor Housing May Crack and Leak

    Maserati is recalling certain 2021-2022 model-year vehicles due to a defective fuel line sensor housing that may crack and leak fuel. The leak can cause engine stall or fire, increasing crash risk.

    Product
    MASERATI — MASERATI QUATTROPORTE, LEVANTE, GHIBLI, MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V871000·2021-11-10

    Ram 1500 Recalled for Inoperable Windshield Defrosting System

    Chrysler is recalling 2022 Ram 1500 vehicles because incompatible HVAC systems may render the windshield defrosting and defogging system inoperable, reducing driver visibility.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0191-2022·2021-11-10

    Lisendo 880 Ultrasound Software displays incorrect cardiac valve measurements

    Lisendo 880 Ultrasound Software versions V1.0–V4.1.3 may not display cardiac measurement results correctly for mitral valve assessments, affecting diagnostic accuracy.

    Product
    Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0195-2022·2021-11-10

    Siemens COVID-19 Diagnostic Assay Recalled for Inadequate Validation Data

    Siemens is recalling Atellica IM SARS-CoV-2 Antigen Assay kits because validation data submitted to the FDA was insufficient to confirm the assay's accuracy for its intended use.

    Product
    Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207861
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V874000·2021-11-10

    Audi Recalls A4, A5, S4, S5, RS 5 Models Due to Air Bag Defect

    Audi is recalling specific 2017-2020 models because a cable fault may disable the passenger air bag, increasing injury risk in a crash.

    Product
    AUDI — AUDI A4, A5, RS 5, S5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0187-2022·2021-11-10

    COVENA PICC Sleeve Recalled for Unauthorized FDA Marketing

    Queen Comfort Products is recalling the COVENA PICC Sleeve, marketed without FDA clearance. Patients currently using the device should contact their healthcare provider immediately.

    Product
    COVENA PICC Sleeve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0200-2022·2021-11-10

    Artis zeego X-Ray System Software Error Affects Image Reconstruction

    Siemens Artis zeego fluoroscopic X-ray systems have a software error that incorrectly displays 3D image reconstruction when the patient table is rotated more than 4 degrees, potentially resulting in incorrect patient treatment during image-guided procedures.

    Product
    Artis zeego, Fluoroscopic X-Ray System Models: 10280959,10502505, 10848283 in combination with the following workplace/system application software models: Product/Model #: syngo X Workplace, 10281061 syngo X Workplace, 10281299 syngo X Workplace, 10502522 Syngo Application…
    Category
    Medical Device
    Distribution
    Distributed nationwide