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.

28701–28725 of 73619

  • ModerateFDA (Drugs)·D-1286-2020·2020-06-10

    Teva Recalls Mixed Amphetamine Salts Tablets Due to Strength Variations

    Teva Pharmaceuticals is recalling 41,348 bottles of 15 mg Mixed Amphetamine Salts tablets because some bottles may contain mixed strengths.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2245-2020·2020-06-10

    Philips Chest Pneumograph Recalled for Missing Natural Rubber Latex Labeling

    Philips is recalling 1,075 Chest Pneumograph units because the labeling fails to state that the product contains natural rubber latex.

    Product
    Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2181-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed, LLC is recalling Osteovationex 3cc Inject Formula bone void fillers because the product may not maintain its setting characteristics for the labeled shelf-life duration.

    Product
    OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2169-2020·2020-06-10

    FDA Recalls Sterile Custom Surgical Packs from Unregistered Facility

    American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2182-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed, LLC is recalling 647 units of Osteovationex 5cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2185-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed is recalling 300 units of Osteovationex 5cc ImpactFormula bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2020·2020-06-10

    FDA Recalls Sterile Custom Surgical Packs Due to Unregistered Facility

    American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2180-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed, LLC is recalling 70 units of Osteovationex 2cc Inject Formula because the product may not maintain its setting characteristics for the labeled shelf-life duration.

    Product
    OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2251-2020·2020-06-10

    Abbott Accelerator APS Aliquoter Module Recalled for Sample Dilution Risk

    Abbott is recalling 11 Accelerator APS Aliquoter Modules because a clot detection error may cause distilled water to dilute samples, leading to incorrect clinical results.

    Product
    Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V340000·2020-06-09

    Mercedes-Benz Metris Recall for Driveshaft Attachment Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vans because the driveshaft may not be attached correctly, risking loss of drive or unexpected airbag deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V337000·2020-06-09

    Jayco Recalls 2020 Motorized RVs Due to Window Glass Detachment Risk

    Jayco is recalling 2020 motorized recreational vehicles because the adhesive on frameless windows may fail, allowing glass to detach and become a projectile.

    Product
    JAYCO — JAYCO, ENTEGRA REDHAWK, QWEST, SENECA, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V335000·2020-06-09

    ARBOC Spirit of America and Liberty Buses Recalled for Fire Risk

    ARBOC is recalling 113 Spirit of America and Spirit of Liberty buses because misrouted power cables may short circuit, increasing the risk of a fire.

    Product
    ARBOC — ARBOC SPIRIT OF AMERICA, SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V334000·2020-06-09

    Chrysler Recalls 2017-2020 Pacifica Plug-in Hybrids for Fire Risk

    Chrysler is recalling 2017-2020 Pacifica Plug-in Hybrids because a high-resistance electrical connection may overheat and cause a fire.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V338000·2020-06-09

    Highland Ridge RV Recalls 2020 Trailers Due to Window Glass Detachment Risk

    Highland Ridge RV is recalling 80 units of 2020 Ridge, Open Range, and Silverstar trailers because window glass may detach and become a projectile.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V339000·2020-06-09

    2020 Thor Motor Coach motorhome frameless windows may detach while driving

    Thor Motor Coach is recalling certain 2020-2021 motorhomes because the adhesive bond in frameless windows may fail, allowing the glass to detach and become a projectile hazard while the vehicle is in motion.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH AXIS, COMPASS, DELANO, GEMINI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V336000·2020-06-09

    Jayco Recalls 2020 Recreational Vehicles Due to Window Glass Detachment Risk

    Jayco is recalling 2020 Eagle, Jay Flight, and other models because window glass may detach and become a projectile.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER EAGLE, JAY FLIGHT, EAGLE HT, NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V333000·2020-06-09

    Lion Recalls 2012-2020 School Buses for Seat Belt Anchor Defect

    Lion Electric Company is recalling 2012-2020 Lion 360 and Lion C school buses because the driver's seat belt anchor may be attached with incorrect hardware, potentially compromising safety in a crash.

    Product
    LION — LION LIONC, 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V331000·2020-06-08

    Ford Recalls Vehicles Due to Door Latch Repair Defects

    Ford is recalling specific 2011-2016 vehicles because previous door latch repairs may have been incomplete, potentially allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN C-MAX, FIESTA, FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E034000·2020-06-08

    Maxon Lift Gates Recalled for Non-Compliant License Plate Light

    Maxon Lift Corp. is recalling specific lift gates where the license plate light may aim rearward, failing federal safety standards and increasing crash risk.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V329000·2020-06-05

    Mercedes-Benz Recalls 2020 GLE and GLS Models for Suspension Defect

    Mercedes-Benz is recalling 2020 GLE 450, GLS 450, and GLS 580 4MATIC vehicles because leaking suspension components may affect handling and increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450, GLS 450, GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V328000·2020-06-05

    Mercedes-Benz Recalls 2020 Models for Rear Seatback Latch Defect

    Mercedes-Benz is recalling 2020 E450, GLC300, and AMG models because the left-rear seatback latch may fail, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, GLC 300, AMG E63S, AMG GLC63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V327000·2020-06-05

    Class C Motorhome Manual Error Increases Rollaway Risk for 2019–2021 Models

    Jayco is recalling certain 2019–2021 Class C motorhomes because the Operator's Manual contains incorrect information about the automatic parking function, which could lead to unintended vehicle movement or rollaway.

    Product
    ENTEGRA — ENTEGRA, JAYCO QWEST, MELBOURNE, MELBOURNE PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V323000·2020-06-04

    Braun Recalls 2019-2020 Demers Ambulances for Rear Brake Line Wear

    Braun Ambulances is recalling 31 Demers ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.

    Product
    DEMERS AMBULANCES — DEMERS AMBULANCES TYPE I (MXP150E), TYPE I (MXP170E)
    Category
    Vehicle
    Distribution
    Distributed nationwide