The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46351–46375 of 73832

  • HighNHTSA·16V715000·2016-10-06

    Newmar Recalls 2017 Motorhomes Due to Power Steering Pump Defect

    Newmar is recalling 2017 King Aire, Essex, London Aire, and Mountain Aire motorhomes because a power steering pump defect may cause intermittent loss of steering assist.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, KING AIRE, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17005·2016-10-06

    Aqua Lung Recalls Powerline Inflators Due to Injury and Drowning Hazards

    Aqua Lung is recalling about 53,000 Powerline inflators because the inflation button can remain depressed, causing uncontrolled ascent and posing injury and drowning hazards.

    Product
    Aqua Lung Powerline inflators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V716000·2016-10-06

    Subaru Recalls 2017 Legacy and Outback for Knee Guard Defect

    Subaru is recalling 2017 Legacy and Outback vehicles because the knee guard bracket may not be properly attached, increasing injury risk in crashes.

    Product
    SUBARU — SUBARU LEGACY, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16T017000·2016-10-06

    GITI Recalls Tires With Sidewall Cracks That May Cause Air Loss

    GITI Tire is recalling specific Primewell, GT Radial, and Dextero tires that may develop sidewall cracks, potentially leading to air loss and tire failure.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17703·2016-10-06

    Wildhorn Outfitters Recalls Camping Hammocks Due to Fall Hazard

    Wildhorn Outfitters is recalling about 9,700 Outpost camping hammocks and suspension kits because cinch buckles can fail, posing a fall hazard.

    Product
    Wildhorn Outfitters Outpost camping hammocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2783-2016·2016-10-05

    Anspach Effort Recalls Light Adaptors for Small Battery Drive Devices

    The Anspach Effort, Inc. is recalling Light Adaptors for Small Battery Drive and Small Battery Drive II devices due to a potential risk of bursting from excessive internal pressure.

    Product
    Light Adaptor for Small Battery Drive and Small Battery Drive II.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2403-2016·2016-10-05

    Bounce Life Style HQ Recalls Cashew Cinnamon for Listeria Risk

    Bounce Life Style HQ is recalling Cashew Cinnamon products due to potential Listeria monocytogenes contamination from recalled sunflower kernels.

    Product
    Australia -Cashew Cinnamon - Caf¿ Bounce, each bulk bag contains 60 pieces, and has UPC 29335805000494
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2404-2016·2016-10-05

    Bounce Energy Balls Recalled for Potential Listeria Contamination

    Bounce Life Style HQ is recalling Bounce Energy Ball Cashew & Pecan Vitality Lift due to potential Listeria monocytogenes contamination from recalled sunflower kernels.

    Product
    Bounce Energy Ball Cashew & Pecan Vitality Lift, each loose unit has net wt 42 gram. The bulk pack (contains 60 pieces) has UPC 9335805000872 and 9335805000308. The jar (contains 40 pieces) has UPC 9335805000254. Bounce Energy Ball Cashew & Pecan Vitality Lift unit has…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2402-2016·2016-10-05

    Bounce Apple Cinnamon Protein Energy Balls Recalled for Listeria Risk

    Bounce Life Style HQ is recalling Apple Cinnamon Protein Energy Balls due to potential Listeria monocytogenes contamination from sunflower kernels.

    Product
    US - Bounce Apple Cinnamon Protein Punch Energy Balls (old name), net wt. 1.48 oz. (42g). Product UPC Codes are 852949003723 (individual packs) and 852949003730 (12-unit boxes). US - Bounce Apple Cinnamon Protein Energy Balls (new name), net wt. 1.48 oz. (42g). Product UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2883-2016·2016-10-05

    Trividia TRUEread Blood Glucose Test Strips Recalled for Incorrect Low Readings

    Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.

    Product
    TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2880-2016·2016-10-05

    Trividia Health Recalls TRUEread Blood Glucose Test Strips for Incorrect Readings

    Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels, potentially affecting patient safety.

    Product
    TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2784-2016·2016-10-05

    Anspach Effort Recalls Small Battery Drive Adaptors Due to Burst Risk

    The Anspach Effort, Inc. is recalling 1,833 Small Battery Drive adaptors worldwide because they may generate excessive internal pressure and burst.

    Product
    Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in traumatology and orthopedic surgery of the skeleton, i.e. drilling, reaming or cutting bone. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V712000·2016-10-05

    Daimler Recalls 2017 Thomas Built Buses Saf-T-Liner C2 School Bus Chassis

    Daimler Trucks North America is recalling 162 model year 2017 Thomas Built Buses Saf-T-Liner C2 school bus chassis because the brake transmission shift interlock may be inoperable.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V709000·2016-10-05

    NHTSA Recalls 2015-2016 Wells Cargo and Haulmark Snowmobile Trailers

    Universal Trailer Cargo Group is recalling 89 aluminum snowmobile trailers because cross winds may cause them to tip or lift, potentially tearing the couplers.

    Product
    WELLS CARGO — WELLS CARGO, HAULMARK ALUMINUM SNOWMOBILE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2896-2016·2016-10-05

    Zyno Medical Administration Set Recalled for Potential Filter Leaking

    Zyno Medical LLC is recalling 47,989 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients.

    Product
    Zyno Medical Administration Set Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: B2-70072-F Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a needle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2882-2016·2016-10-05

    Trividia Health Recalls TRUEread Blood Glucose Test Strips for Inaccurate Readings

    Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels. The recall affects strips and kits distributed in the US and internationally.

    Product
    TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2886-2016·2016-10-05

    Spacelabs Xhibit Telemetry Receiver Recall for System Lockups

    Spacelabs Healthcare is recalling Xhibit Telemetry Receivers because the system may go offline or lock up, potentially failing to display alarms.

    Product
    Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2877-2016·2016-10-05

    Siemens PRIMUS Linear Accelerators Recalled for Software Safety Issues

    Siemens Medical Solutions is recalling 103 PRIMUS linear accelerators to install a software patch addressing several safety issues.

    Product
    PRIMUS, Accelerator, Linear, Medical The PRIMUSTM family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2895-2016·2016-10-05

    Zyno Medical Administration Set Recalled for Potential Filter Leaking

    Zyno Medical LLC is recalling 78,063 sterile administration sets due to a potential filter leaking defect. The sets are distributed nationwide for use with infusion pumps or gravity feed.

    Product
    Zyno Medical Administration Set, Sterile. RX For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: B2-70071-DF Product Code: B2-70071-DF-120 (expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2888-2016·2016-10-05

    Spiegelberg Brain Pressure Monitoring Probes Recalled for Measurement Errors

    Spiegelberg is recalling 22 Brain Pressure Monitoring System probes due to air chamber shrinkage that caused false high readings in the lower measuring range.

    Product
    Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: SNDI3.1.63/FV535P Product Usage: lntracranial pressure measuring probes are used to measure intracranial pressure (intracranial pressure, ICP), so the pressure in the head.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2881-2016·2016-10-05

    Trividia Health Recalls TRUEread Blood Glucose Test Strips for Inaccurate Readings

    Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.

    Product
    TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V710000·2016-10-05

    Altec Recalls 2014-2015 Aerial Devices Due to Boom Tip Cover Defect

    Altec is recalling 219 model year 2014-2015 aerial devices because an improperly sized boom tip cover opening may allow contact with energized conductors, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2893-2016·2016-10-05

    Zyno Medical Administration Set Recalled for Potential Filter Leaking

    Zyno Medical LLC is recalling 114,081 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients' vascular systems.

    Product
    Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80071-DF Product Code: A2-80071-DF-120 (Expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide