The Recall Desk

State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47451–47475 of 73840

  • HighFDA (Devices)·Z-2227-2016·2016-07-27

    WalkMed Recalls IV Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific lots of IV sets with 0.22 micron filters due to the potential presence of particulate matter in or on the devices.

    Product
    T095-022, IV Set with 0.22 Micron Filter. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2233-2016·2016-07-27

    WalkMed Infusion Recalls Triton Administration Sets Due to Particulate Presence

    WalkMed Infusion is voluntarily recalling Triton Administration Sets due to the potential presence of particulate matter in or on the devices.

    Product
    T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2240-2016·2016-07-27

    Biomet Recalls TSP Hip Fracture Plating System Due to Screw Fracture Risk

    Biomet, Inc. is recalling 5,458 units of the TSP Hip Fracture Plating System because screws may fracture during implantation, potentially leaving a foreign body in the patient.

    Product
    TSP Hip Fracture Plating System device, fixation, proximal femoral, implant The Biomet Hip Fracture Plating Systems are indicated for use in the open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2231-2016·2016-07-27

    WalkMed Recalls IV Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.

    Product
    T100-000WF, IV Set with Upper Y-Site, Lower Y-Site, Back Check Valve, and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1702-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause them to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Vanilla Bean Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 11 oz./325 mL - item number PPV3BF9; 15.2 oz/450 mL item number: PPV4BF6;- US; 32 oz./946 mL; item number PPVQBF6 - US, PPVQBC6 - Canada: Selling…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1701-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Chocolate Protein Plus: 22 g protein per bottle + 21 vitamins & minerals. Packaged in 11 oz./325 mL - item number PPC3BF9; 15.2 oz/450 mL I item number: PPC4BF6;- US; PPC4BC6 - Canada; 32 oz./946 mL; item number PPCQBF6 - US, PPCQBC6 - Canada…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1707-2016·2016-07-27

    Bolthouse Farms Recalls Protein Drinks Due to Spoilage and Unpleasant Taste

    Bolthouse Farms is recalling 8 varieties of protein drinks because spoilage may cause them to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Mocha Cappuccino Perfectly Protein : 30 g protein per bottle + 21 vitamins & minerals. Packaged in 15.2 oz/946 mL.- item number MC4BF6 - US and MC4BC6 - Canada; 32 oz./946 mL item number: MCQBF6 - US; MCQBC6 - Canada Selling Unit UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1706-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Banana Honey Almond Butter Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 11 oz/450 mL item number: PPH3BF9; 15.0 oz/946 mL. - item number PPH4BF6; Selling Unit UPC Case GTIN 11…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2245-2016·2016-07-27

    Siemens Syngo.via PACS Software Recalled for Incorrect Volume Calculations

    Siemens Medical Solutions is recalling 50 units of Syngo.via PACS software due to incorrect volume calculation values. A software update is available to resolve the error.

    Product
    Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing, manipulation, communication, and storage of medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1704-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Coconut Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 15.2 oz/450 mL item number: PPCN4BF6; Selling Unit UPC Case GTIN 15.2 oz. 0-71464-01892-4…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1703-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Coffee Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 11 oz./325 mL - item number PPJ3BF9; 15.2 oz/450 mL item number: PPJ4BF6; 32 oz./946 mL; item number PPJQBF6: Selling Unit UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2256-2016·2016-07-27

    Siemens ADVIA Centaur XPT Software Recalled for Potential Result Errors

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur XPT system software versions V1.0.1 through V1.1 due to eight identified issues that may affect test results.

    Product
    ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN 10819704), V1.0.2 (Bundle 1.0.1086 SMN 11219806), V1.0.3 (Bundle 1.0.1108 SMN 11220781) and V1.1 (Bundle 1.1.243 SMN 11221979). Product Usage: This system is intended for professional use in a laboratory…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2225-2016·2016-07-27

    WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific IV administration sets due to the potential presence of particulate matter in or on the devices.

    Product
    T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Back Check Valve. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2016·2016-07-27

    WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes

    WalkMed Infusion is recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.

    Product
    The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1705-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Strawberry Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 15.2 oz/450 mL item number: PPCN4BF6; 32 oz/946 mL. - item number PPSWQBF6 Selling Unit UPC Case GTIN 15.2 oz.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2214-2016·2016-07-27

    DePuy Synthes Recalls TFNA Blade/Screw Guide Sleeves Due to Sizing Defect

    DePuy Synthes is voluntarily recalling TFNA Blade/Screw Guide Sleeves because a manufacturing defect may prevent proper use, potentially causing surgical delays.

    Product
    Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part Number ID 03.037.017, Class I exempt Lot Numbers: 9066399; 9066435; 9409790; 9519308; 9620447; 9301183; 9409792; 9519303; 9641077; 9301184; 9409791; 9542998…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1446-2016·2016-07-27

    Sun Pharmaceutical Recalls Bupropion Hydrochloride Tablets for Dissolution Failure

    Sun Pharmaceutical Industries is recalling 16,085 bottles of Bupropion Hydrochloride Extended Release Tablets because they failed dissolution specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V558000·2016-07-26

    Forest River Recalls 2011-2016 Glaval Titan II Buses for Frame Cracks

    Forest River is recalling 39 Glaval Titan II Low Floor buses due to frames that may crack, potentially reducing driver control and increasing crash risk.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V559000·2016-07-26

    2015 RAM 2500 and 3500 Recalled for Steering Bracket Weld Defect

    Chrysler is recalling 2015 RAM 2500 and 3500 trucks because inadequate welds on front track bar brackets may separate, reducing steering response and increasing crash risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V557000·2016-07-26

    Load Trail Triple Axle Tilt Deck Trailers Recalled for Weld Defects

    Load Trail is recalling 2014-2016 Triple Axle Tilt Deck trailers because weld joints may crack, potentially causing equipment to disengage and increasing crash risk.

    Product
    LOAD TRAIL — LOAD TRAIL TRIPLE AXLE TILT DECK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16759·2016-07-26

    Electrolux Recalls Frigidaire and Kenmore Wall Ovens Due to Fire Hazard

    Electrolux is recalling about 1,000 Frigidaire and Kenmore electric wall ovens because a malfunctioning thermal switch poses a fire hazard. No injuries have been reported.

    Product
    Electric wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16760·2016-07-26

    Inovonics Recalls Emergency Transmitters and Receivers Due to Signal Failure

    Inovonics is recalling about 5,500 emergency transmitters and receivers because they may fail to send or receive help signals. No injuries have been reported.

    Product
    Inovonics pendant transmitters, universal transmitters and add-on receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide