The Recall Desk

State

Northern Mariana Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42851–42875 of 73829

  • LowFDA (Drugs)·D-0912-2017·2017-06-21

    Pharmedium Recalls Potassium Phosphate IV Bags Due to Labeling Error

    Pharmedium Services is recalling 48 bags of Potassium Phosphate IV solution because the printed volume on the label is incorrect.

    Product
    Potassium PHOSphate added to 0.9% Sodium Chloride, 20 mMol 100 mL Bag, Service Code 2K5287, NDC# 61553-0287-48, Total Volume 100.00 mL incorrectly labeled as106.67 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0920-2017·2017-06-21

    Mylan Recalls Montelukast Sodium Oral Granules Due to Impurity Failures

    Mylan Pharmaceuticals is recalling 11,624 pouches of Montelukast Sodium Oral Granules, 4 mg, due to failed impurity specifications.

    Product
    Montelukast Sodium Oral Granules, 4 mg pouch, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-6040-93
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0907-2017·2017-06-21

    Pharmedium Recalls Potassium Chloride Bags With Incorrect Volume Labeling

    Pharmedium Services, LLC is recalling 143 bags of Potassium Chloride in 0.9% Sodium Chloride because the product label incorrectly states the total volume as 105.00 mL instead of 100.00 mL.

    Product
    Potassium CHLORide added to 0.9% Sodium Chloride, 10mEq 100 mL Bag, Service Code 2K5856, NDC# 61553-0856-48, Total Volume 100.00 mL incorrectly labeled as 105.00 mL, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0911-2017·2017-06-21

    Pharmedium Recalls Potassium Phosphate IV Bags Due to Incorrect Volume Labeling

    Pharmedium Services, LLC is recalling 672 bags of Potassium Phosphate IV solution because the printed volume on the label is incorrect.

    Product
    Potassium PHOSphate added to 0.9% Sodium Chloride, 10 mMol 100 mL Bag, Service Code 2K5288, NDC# 61553-0288-48, Total Volume 100.00 mL incorrectly labeled as 103.33 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E029000·2017-06-20

    Cummins Recalls X15 Diesel Engines Due to Fuel Pump Gear Slip

    Cummins is recalling X15 heavy-duty diesel engines because a fuel pump drive gear may slip, causing engine stalls and increasing crash risk.

    Product
    FUEL SYSTEM, DIESEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V388000·2017-06-20

    KTM Recalls 2016-2017 690 Duke Motorcycles for Fuel Leak Risk

    KTM is recalling 2016-2017 690 Duke motorcycles because the fuel tank filler cap area may leak, increasing the risk of fire or injury.

    Product
    KTM — KTM 690 DUKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17751·2017-06-20

    Kawasaki Recalls Utility and Off-Highway Vehicles Due to Fire Hazard

    Kawasaki is recalling approximately 6,600 utility, recreational off-highway, and all-terrain vehicles because a fuel gauge retainer can collapse and leak fuel, posing a fire hazard.

    Product
    Utility vehicles, recreational off-highway vehicles and all-terrain vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17180·2017-06-20

    Staples Recalls Hazen Mesh Task Chairs Due to Fall Hazard

    Staples is recalling Hazen Mesh Task chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact Staples for a free replacement base.

    Product
    Hazen Mesh Task chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowNHTSA·17V387000·2017-06-20

    KZRV Recalls 2018 Recreational Trailers Due to Missing Certification Date

    KZRV is recalling 2018 recreational trailers because the Federal Certification label lacks the manufacturing date, potentially preventing owners from identifying other safety recalls.

    Product
    KZRV — KZRV VENOM, SPORTSMEN SPORTSTER, SPREE, SPORT TREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V386000·2017-06-19

    BYD Recalls 2015-2016 K7 M Buses for Wiper Arm Defect

    BYD is recalling 2015-2016 K7 M buses because wiper arms may crack and detach, reducing visibility and increasing crash risk.

    Product
    BYD — BYD K7 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V385000·2017-06-19

    Starcraft RV Recalls 2018 Launch Outfitter Trailers for Electrical Outlet Defect

    Starcraft RV is recalling 2018 Launch Outfitter travel trailers because an electrical outlet lacks Ground Fault Circuit Interrupter protection, increasing the risk of electrical shock.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·075-2017·2017-06-17

    Supreme Cuisine Recalls Meat and Poultry Fat Products Due to Processing Deviation

    Supreme Cuisine is recalling approximately 325,000 pounds of meat and poultry fat and lard products due to a processing deviation that may allow bacterial pathogens to grow.

    Product
    Supreme Cuisine Recalls Meat and Poultry Fat and Lard Products Due to Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17750·2017-06-16

    Advanced Composites Recalls Bicycle Forks Due to Fall Hazard

    Advanced Composites is recalling about 40 Wound Up Tandem Duo Disc bicycle forks because the fork leg can crack, posing a fall hazard.

    Product
    Bicycle forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V381000·2017-06-15

    Thor Motor Coach Recalls 2018 Outlaw 29H Motorhomes for Fire Risk

    Thor Motor Coach is recalling 2018 Outlaw 29H motorhomes because an incorrect fuse size may increase the risk of a fire if the awning light circuit short circuits.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V382000·2017-06-15

    GM Recalls 2014-2016 Chevrolet SS Vehicles for Steering Defect

    General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion may cause a loss of electric power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2283-2017·2017-06-14

    Arrow VPS Access Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2225-2017·2017-06-14

    Magellan LeadCare Blood Lead Test Kits Recalled for Underestimating Results

    Magellan Diagnostics is recalling LeadCare and LeadCare II test kits because they may underestimate lead concentrations in venous blood samples.

    Product
    Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage: The LeadCare Blood Lead Test Kit is for in vitro diagnostic use only. The Test Kit is for the quantitative measurement of lead in fresh whole blood. This product is for professional use only. Sensors…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2246-2017·2017-06-14

    Baxter MiniCap PD Transfer Set Recalled for Connection Leak Risk

    Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets because connection issues may cause leaks and contamination, potentially leading to peritonitis.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit. Sterile. Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2253-2017·2017-06-14

    Arrow International Recalls Central Venous Access Kits Due to Needlestick Risk

    Arrow International is recalling MAC Two-Lumen Central Venous Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access Device, Integral Hemostasis Valve, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2299-2017·2017-06-14

    Arrow Arterial Catheterization Kits Recalled for Needlestick Injury Risk

    Arrow International is recalling Arterial Catheterization Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.

    Product
    Arterial Catheterization Kit with Maximal Barrier Precautions The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
    Category
    Medical Device
    Distribution
    Distributed nationwide