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.

22601–22625 of 73501

  • HighFDA (Devices)·Z-0325-2022·2021-12-08

    Hurricane RX Dilation Balloon Recalled Due to Pinhole Defect Causing Pressure Loss

    Boston Scientific is recalling certain lots of the Hurricane RX Dilation Balloon due to a pinhole defect that causes loss of pressure or prevents the balloon from gaining or maintaining pressure during use, potentially prolonging medical procedures.

    Product
    HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545940
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0240-2022·2021-12-08

    Polar Black Cherry Premium Seltzer recalled for unlabeled sulfites

    Keurig Dr Pepper is recalling Polar Black Cherry Premium Seltzer 12-packs due to unlabeled sulfites. The recall affects 7,849 cases distributed nationwide with product code date 12/16/2022.

    Product
    Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0323-2022·2021-12-08

    Boston Scientific HURRICANE RX Dilation Balloon Pressure Loss Recalled

    Boston Scientific is recalling HURRICANE RX Dilation Balloons across the US due to pinhole defects that cause pressure loss during endoscopic procedures. The defect may prolong procedures and affect patient safety.

    Product
    HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545920
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0324-2022·2021-12-08

    Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect

    Boston Scientific is recalling the Hurricane RX Dilation Balloon nationwide due to a pinhole defect causing loss of pressure or failure to maintain pressure during endoscopic procedures used to treat biliary strictures.

    Product
    HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545930
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0329-2022·2021-12-08

    GE Centricity Medical Imaging Software May Display Incomplete Patient Studies

    GE Healthcare recalled versions of Centricity Universal Viewer Zero Footprint Client software due to a potential defect that could display incomplete patient imaging studies. No injuries have been reported.

    Product
    GE Centricity Universal Viewer Zero Footprint Client
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V948000·2021-12-08

    Carson Fun Runner Trailers Recalled for Potential Gas Leak Risk

    Carson is recalling 2018-2020 Fun Runner FC20 trailers because an overtightened bolt may damage the stove's o-ring, causing a gas leak that increases fire risk.

    Product
    CARSON — CARSON FUN RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0316-2022·2021-12-08

    INBONE Total Ankle System Recalled Due to Package Labeling Mismatch

    Wright Medical Technology is recalling the INBONE Total Ankle System because package contents do not match the package labeling on affected units distributed in Michigan and Pennsylvania.

    Product
    INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0264-2022·2021-12-08

    Tydemy Oral Contraceptive Recalled Due to Subpotent Drug

    Lupin Pharmaceuticals has recalled Tydemy oral contraceptive tablets nationwide due to subpotency. The recall affects 4,113 cartons distributed throughout the United States.

    Product
    Tydemy (drospirenone, ethinyl estradiol & levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets, 0.451 mg), packaged in cartons containing 3 wallets of 28 Tablets each, Rx Only, Distributed by: Lupin Pharmaceuticals, Inc., Baltimore, Maryland…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V943000·2021-12-07

    Great Dane Recalls 2022 Trailers Due to Wheel Hub Lubrication Defect

    Great Dane is recalling 2022 Champion and Everest trailers because insufficient wheel hub lubrication could cause bearing failure and loss of control.

    Product
    GREAT DANE — GREAT DANE CHAMPION, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22025·2021-12-06

    Drive DeVilbiss Adult Bed Rails Recalled; Two Deaths from Entrapment

    Drive DeVilbiss Healthcare is recalling four models of adult portable bed rails that can trap users between the rail and mattress, causing asphyxiation. Two deaths have been reported.

    Product
    Bed Assist Handles and Bed Assist Rail
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·046-2021·2021-12-05

    Alexander & Hornung Recalls Fully Cooked Pork Products Due to Listeria

    Alexander & Hornung is recalling approximately 2.3 million pounds of fully cooked ham and pepperoni products due to possible Listeria monocytogenes contamination.

    Product
    Alexander & Hornung Recalls Fully Cooked Pork Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·045-2021·2021-12-03

    Erie Meat Products Recalls Chicken Bologna Imported Without Inspection

    Erie Meat Products Ltd. is recalling approximately 1,224 pounds of chicken bologna imported into the U.S. without FSIS reinspection. The products were distributed to correctional institutions in four states.

    Product
    Erie Meat Products Ltd. Recalls Chicken Bologna Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V940000·2021-12-03

    Zero Motorcycles Recalls 2022 SR Models Due to Incorrect Rear Brake Pads

    Zero Motorcycles is recalling 2022 SR, SR/F, and SR/S motorcycles because incorrect rear brake pads were installed, which may not work as intended and increase crash risk.

    Product
    ZERO — ZERO SR, SR/F, SR/S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V937000·2021-12-02

    2021 Hyundai Accent brake master cylinder defect recall

    Hyundai is recalling certain 2021 Accent vehicles due to a brake master cylinder defect. The component may have sharp edges that damage the inner oil seal, reducing braking performance and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V938000·2021-12-02

    2022 Hyundai Tucson: Inoperative Headlights and Taillights from Software Defect

    Hyundai is recalling 2022 Tucson vehicles with incompatible ICU software that can disable headlights and taillights, reducing visibility and increasing crash risk. All affected vehicles have been repaired.

    Product
    HYUNDAI — HYUNDAI TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V939000·2021-12-02

    2021 Acura RDX Driveshaft Defect May Cause Loss of Drive Power

    Honda is recalling certain 2021 Acura RDX vehicles because the front driveshaft may have been improperly heat-treated, potentially causing driveshaft failure and sudden loss of drive power or vehicle rollaway.

    Product
    ACURA — ACURA, HONDA RDX, CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E099000·2021-12-01

    Cummins Recalls X12 Diesel Engines Due to Fuel Tube Cracking Risk

    Cummins is recalling X12 Diesel Engines because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0214-2022·2021-12-01

    MaryRuth's Organic Infants Liquid Probiotic Recalled for Bacterial Contamination

    MaryRuth's Organic Infants Liquid Probiotic dietary supplement is being recalled because internal testing found Pseudomonas aeruginosa contamination. The affected product is distributed nationwide.

    Product
    MaryRuth's Organic Infants Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL) UPC: 8 56645 00858 7 Serving size (five drops - start with one and work up to 5) Organic Proprietary Probiotic Blend 250 mg. Bifidobacterium lactis Bifidobacterium infantis…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·22024·2021-12-01

    Halo Recalls Children's Projector Flashlights for Button Battery Hazard

    HALO Branded Solutions Inc. is recalling about 82,500 children's projector flashlights distributed in care packages because children can disassemble them and access button cell batteries, creating ingestion and choking hazards. Two incidents have been reported, including one requiring surgery.

    Product
    Projector Flashlights (included as part of a care package)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V934000·2021-12-01

    Mercedes-Benz Recalls 2021 Sprinter Vans for Rear Step Bolt Issue

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because improperly tightened rear step bolts could allow the step to separate, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 2500, SPRINTER 1500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22023·2021-12-01

    DEWALT Jobsite Pro Wireless Earphones Recalled for Burn and Fire Hazards

    E-filliate is recalling about 301,800 DEWALT Jobsite Pro Wireless Earphones because they can overheat during charging or use, posing burn and fire hazards. The company has received 61 reports of overheating, including five fires and four minor burn injuries.

    Product
    DEWALT ® Jobsite Pro Wireless Earphones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V933000·2021-12-01

    2021 Mercedes-Benz Sprinter Vehicles Recalled for Brake Hose Damage Risk

    Daimler Vans USA is recalling 2021 Mercedes-Benz and Freightliner Sprinter vans because the front fender liner may damage the brake hose, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide