The Recall Desk

State

Northern Mariana Islands product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19426–19450 of 73399

  • HighNHTSA·22V625000·2022-08-15

    Spartan Fire Recalls One 2022 MetroStar Fire Truck for Engine Defect

    Spartan Fire is recalling one 2022 MetroStar fire truck because the engine control module may short-circuit, causing an unexpected engine shutdown that increases crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V627000·2022-08-15

    2020-2021 Hyundai Palisade windshield wiper motor failure recall

    Hyundai is recalling certain 2020-2021 Palisade vehicles due to windshield wiper motor failure. The inoperative wipers reduce visibility and increase crash risk.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V626000·2022-08-15

    2020-2022 Kia Telluride tow hitch electrical short fire hazard

    Certain 2020-2022 Kia Telluride vehicles with Genuine Kia tow hitch harnesses may experience electrical shorts from debris and moisture, creating a fire risk while parked or driving.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V622000·2022-08-12

    Seagrave Recalls 2022 Marauder Fire Trucks Due to Steering Gear Defect

    Seagrave is recalling 2022 Marauder fire trucks because incorrectly assembled steering gears may fracture, potentially causing a loss of steering control and increasing crash risk.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V623000·2022-08-12

    Ford Recalls 2021-2022 F-150 Trucks for Driveshaft Fracture Risk

    Ford is recalling 2021-2022 F-150 vehicles because underbody insulators may loosen and damage the driveshaft, potentially causing loss of vehicle control.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22199·2022-08-11

    Residential Elevators recalled for child entrapment hazard

    Residential Elevators, Inc. is recalling about 31,000 home elevators sold since 1986 because young children can become trapped between the exterior and interior doors, risking serious injury or death.

    Product
    Residential Elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V619000·2022-08-11

    2022 Chrysler Pacifica windshield wipers may not function due to loose arm nuts

    Certain 2022 Chrysler Pacifica and Voyager vehicles have improperly tightened windshield wiper arm nuts, causing malfunction. This reduces driver visibility and increases crash risk. Dealers will tighten the nuts free of charge.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V620000·2022-08-11

    Rosenbauer Fire Trucks Recalled for Engine Control Module Short-Circuit Risk

    Rosenbauer America is recalling 2022 Commander and 2023 Commercial M2-106 fire trucks because an engine control module short-circuit may cause unexpected engine shutdown.

    Product
    ROSENBAUER — ROSENBAUER COMMERCIAL M2-106, COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V618000·2022-08-11

    2023 Grand Design Momentum fifth wheels ramp door fall hazard

    Grand Design is recalling 2023 and 2022 Momentum fifth wheels due to a defective ramp door cut-off switch that may allow the electric ramp door to fall, creating an injury risk.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22766·2022-08-11

    Footpads for Onewheel GT Electric Skateboards Recalled for Injury Hazard

    Future Motion is recalling front footpads for Onewheel GT electric skateboards because the footpad can fail to disengage after the rider dismounts, causing the skateboard to continue operating and potentially injure bystanders.

    Product
    Footpads for Onewheel GT Electric Skateboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V617000·2022-08-11

    Third-Row Seat Belt Buckle Rivet Defect in 2021-2022 GMC Yukon and Related Vehicles

    General Motors is recalling 484,155 vehicles with improperly formed rivets on third-row seat belt buckle assemblies. The defect may prevent proper seat belt restraint in a crash, increasing injury risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1514-2022·2022-08-10

    Honey supplement recalled nationwide for undeclared sildenafil content

    Kingdom Honey Royal Honey VIP is recalled due to undeclared sildenafil, a pharmaceutical ingredient. The product was distributed nationwide; all lots are affected.

    Product
    Kingdom Honey Royal Honey VIP The Ultimate Power Source; 12 sachets-20g; UPC 555755 800036
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V614000·2022-08-10

    BMW Recalls 2018 540D xDrive Vehicles Due to EGR Module Fire Risk

    BMW is recalling 2018 540D xDrive vehicles because an internal leak in the EGR cooler may cause coolant to mix with soot, creating smoldering particles and a melting intake manifold that increases fire risk.

    Product
    BMW — BMW 540D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1333-2022·2022-08-10

    SANGTER Energy Supplement Capsules Recalled for Undisclosed Sildenafil

    Distributor RFR, LLC is recalling SANGTER Energy Supplement Capsules because FDA analysis found they contain undisclosed sildenafil without FDA approval. The product was distributed nationwide and internationally.

    Product
    SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1401-2022·2022-08-10

    SARS-CoV-2 Rapid Antigen Test Kits Distributed Without FDA Approval

    North American Diagnostics is recalling SARS-CoV-2 rapid antigen test kits that were distributed without FDA approval or clearance. Approximately 122,366 units were sold to consumers across multiple US states and internationally.

    Product
    SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML LDT Kits, SML Brand Finished Kits, SML Brand BT Test Kits, SML Brand BT Antigen Test Kit LDT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1350-2022·2022-08-10

    SUSTANGO supplement capsules recalled for undisclosed tadalafil content

    SUSTANGO capsules contain the undisclosed pharmaceutical ingredient tadalafil and were marketed without FDA approval. Approximately 750 cartons were distributed nationwide via Amazon.

    Product
    SUSTANGO (Pendenadril Tytrate Blend) Capsules, 400 mg, 10-count blisters per carton, Formulated by: Male FX Labs, Bangor, ME, ASIN X0024468I9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2022·2022-08-10

    PRESTIGE RETRACTION GRASPER recalled due to potential weld separation

    The FDA is recalling 399 units of the PRESTIGE RETRACTION GRASPER surgical instrument due to risk of weld separation between the handle and shaft. This defect could cause device malfunction during surgical procedures.

    Product
    PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1498-2022·2022-08-10

    Atellica CH Iron_2 Diagnostic Device Produces False Microalbumin Results from Reagent Carryover

    Siemens Atellica CH Iron_2 in vitro diagnostic devices are being recalled because they produce falsely elevated microalbumin test results when a microalbumin test immediately follows an iron test. No illnesses have been reported.

    Product
    Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and (lithium heparin) plasma samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1303-2022·2022-08-10

    Matzim LA Extended-Release Tablets Recalled for Dissolution Specification Failure

    Matzim LA Extended-Release Tablets, 240 mg are being recalled due to failed dissolution specifications. Patients taking this medication should consult their doctor about their treatment.

    Product
    Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL USA 33314, USA, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054 USA; NDC 58544-692-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1481-2022·2022-08-10

    Endoscopic Grasper Instruments Recalled Due to Weld Separation Risk

    Aesculap Implant Systems is recalling PRESTIGE ATRAUMATIC GRASPER surgical instruments because the weld connecting the handle to the shaft may separate during use.

    Product
    PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
    Category
    Medical Device
    Distribution
    Distributed nationwide