The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59101–59125 of 73856

  • HighFDA (Devices)·Z-1115-2014·2014-03-05

    Winco Convalescent Recliners Recalled for Recline Mechanism Defect

    Winco Mfg. is recalling 369 convalescent recliners due to a manufacturing defect in the right hand recline mechanism that may cause the position lock bar to lose functionality.

    Product
    CONVALESCENT RECLINER 5251/5261, 525S/526S with Side Storage Pocket, Upholstered side-panels, Recessed hand-grips, Webbed suspension seating, Non-porous tray. The products are a multi position recliners with a steel frame used primarily in long term care or convalescent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1101-2014·2014-03-05

    Fresenius Optiflux F180NR Dialyzers Recalled for Dialysate Port Leak

    Fresenius Medical Care is recalling Optiflux F180NR dialyzers due to a dialysate port leak during priming. The recall covers 52,752 units distributed in the US and Mexico.

    Product
    Optiflux F180NR High Flux Dialyzers; Product Number: 0500318N. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14E006000·2014-03-05

    Meritor Wabco Recalls Trailer Spring Brake Control Valves

    Meritor Wabco is recalling specific trailer spring brake control valves sold as replacement parts because the intake/exhaust valve may come apart, preventing the parking brake from engaging.

    Product
    PARKING BRAKE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0978-2014·2014-03-05

    Elekta Recalls DMLC IV-ERGO Systems Due to Gantry Sensor Error

    Elekta, Inc. is recalling 35 DMLC IV-ERGO systems because an intermittent error may occur in the gantry sensor. The devices are used with linear accelerators for radiation therapy.

    Product
    DMLC IV-ERGO Product Usage: Intended for use with rotating gantry linear accelerators to conform radiation dose delivery to geometrical volumes of specific shape containing pathology to be treated so that adjacent non-diseased tissues are spared to the extent possible.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1118-2014·2014-03-05

    Philips HeartStart MRx Monitor/Defibrillator Recalled for ECG Cable Wear

    Philips is recalling HeartStart MRx Monitor/Defibrillators because the ECG trunk cable and connector block may wear prematurely, causing an interrupted ECG signal.

    Product
    Philips HeartStart MRx Monitor/Defibrillator; Models: M3535A, M3536A, M3536J, M3536M, M3536M5, and M3536MC. Used for the termination of ventricular tachycardia and ventricular fibrillation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1562-2014·2014-03-05

    Newman's Own Salsa Con Queso Recalled for Undeclared Wheat

    Newman's Own is recalling Salsa Con Queso, Medium All Natural, 16 oz. jars nationwide due to undeclared wheat.

    Product
    Newman's Own Salsa Con Queso, Medium All Natural Net Wt.16 oz., packaged in a glass jar UPC 0 20662 00353 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1114-2014·2014-03-05

    Winco Premier Care Recliner 5570 Recalled for Lock Bar Defect

    Winco Mfg. is recalling 369 Premier Care Recliner 5570 units due to a manufacturing defect that may cause the lock bar to fail.

    Product
    PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered, OPTIONAL Heat or Heat & Massage, OPTIONAL LiquiCell. The products are a multi position recliners with a steel frame used primarily in long term care or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1120-2014·2014-03-05

    Philips HeartStart MRx Defibrillator Batteries Recalled for Shutdown Risk

    Philips is recalling 43,792 HeartStart MRx defibrillator batteries because they may shut down unexpectedly when exposed to high electromagnetic interference.

    Product
    HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1097-2014·2014-03-05

    Ossur Recalls Symbionic Leg Due to Battery Warning Failure

    Ossur is recalling 144 Symbionic Leg prosthetics because they fail to display a low battery warning before powering down.

    Product
    The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral and knee disarticulation amputees. Product Usage: SYMBIONIC LEG is intended for continuous use by amputees of low to moderate impact levels that weigh less than 125 kg for foot categories 25 30 and less…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1553-2014·2014-03-05

    Popcorn Factory Recalls Heart-Shaped Popcorn Balls Due to Missing Allergen Labels

    The Popcorn Factory is recalling heart-shaped popcorn balls because the Nutrition Facts and allergen labels were not applied to the individual pieces. The product contains milk and soy allergens.

    Product
    Candy coated popcorn shaped into a heart weighing 1.5 ounces per piece and individually wrapped in clear plastic packaging. There are 24 popcorn balls per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1099-2014·2014-03-05

    Fresenius Optiflux F160NR Dialyzers Recalled for Dialysate Port Leak

    Fresenius Medical Care is recalling Optiflux F160NR dialyzers because the dialysate port may leak during priming. The recall covers 6,720 units distributed in the US and Mexico.

    Product
    Optiflux F160NR High Flux Dialyzers; Product Number: 0500316N. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1075-2014·2014-03-05

    Radiometer D788 pCO2 Membranes Recalled for Biased Measurement Results

    Radiometer America is recalling D788 pCO2 membranes because they may cause biased measurement results for patients and quality control.

    Product
    pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument used to identify and quantify two or more gases, and sometimes electrolytes, in whole blood using multiple special electrodes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1106-2014·2014-03-05

    Fresenius Recalls Optiflux F18Nre Dialyzers Due to Port Leak Risk

    Fresenius Medical Care is recalling 34,752 Optiflux F18Nre Flux Dialyzers because the dialysate port may leak during priming.

    Product
    Optiflux F18Nre Flux Dialyzers; Product Number: 0500308E. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1080-2014·2014-03-05

    Siemens Artis zee Ceiling Systems Recalled for Cable Damage Risk

    Siemens Medical Solutions USA is recalling 284 Artis zee Ceiling Systems due to potential cable damage from sub-optimal guidance.

    Product
    Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1103-2014·2014-03-05

    Fresenius Optiflux F200NR Dialyzers Recalled for Dialysate Port Leak

    Fresenius Medical Care is recalling 19,596 Optiflux F200NR dialyzers due to a dialysate port leak during priming. The units were distributed in the US and Mexico.

    Product
    Optiflux F200NR High Flux Dialyzers; Product Number: 0500320N. Single Use acute or chronic hemanalysis treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1567-2014·2014-03-05

    Mars Recalls Uncle Ben's Saffron Rice Due to Mild Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Saffron Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Saffron Flavor, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-11547
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1088-2014·2014-03-05

    Actavis Recalls Subpotent Gelnique Oxybutynin Chloride Gel Samples

    Actavis is recalling Gelnique (oxybutynin chloride) Gel 10% physician samples because drug potency was compromised during shipment.

    Product
    Gelnique (oxybutynin chloride) Gel 10%, 100 mg in 1 g sachet, for topical use only. Physician sample in clamshell container with seven heat-sealed sachets. Rx Only. Watson Pharmaceuticals Inc, Corona, CA, 92890. NDC: 52544-084-77.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1564-2014·2014-03-05

    Mars Recalls Uncle Ben's Rice Due to Mild Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Roasted Chicken Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Roasted Chicken Flavor, net weight 5 LB (2.27 kg) and 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1563-2014·2014-03-05

    Mars Recalls Uncle Ben's Infused Rice Mexican Flavor Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Mexican Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Mexican Flavor, net weight 5 LB (2.27 kg) and 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1590-2014·2014-03-05

    Mars Recalls Uncle Ben's Infused Rice Cheese Flavor Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Cheese Flavor nationwide after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Cheese Flavor, net weight 5 LB (2.27 kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-1547
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1087-2014·2014-03-05

    Ortho VITROS Sodium Slides Recalled for False Positive Results

    Ortho Clinical Diagnostics is recalling VITROS Na+ Slides and Calibrator Kit 2 because they may produce false positive sodium results in serum and plasma samples.

    Product
    VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY 14652 VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1087-2014·2014-03-05

    Actavis Recalls Clonazepam Tablets Due to Subpotent Tablet Weight

    Actavis Elizabeth LLC is recalling 13,608 bottles of Clonazepam 2 mg tablets because routine testing found one tablet with weight below specification.

    Product
    Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA NDC 0228-3005-11 packaged in White/Round HDPE 75 CC with white/round plastic 33 mm CRC closure shipped in corrugated 75 cc carton (24 bottles/carton)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1094-2014·2014-03-05

    Hologic Recalls NovaSure Radiofrequency Controllers for Electrical Standard Non-Compliance

    Hologic is recalling 93 NovaSure Radiofrequency Controllers because they may not meet the IEC 60601-1 electrical safety standard.

    Product
    NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency Controller, Model Number: 71978-001 Catalog Number: RFC2009 Product Usage: The NovaSure Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in…
    Category
    Medical Device
    Distribution
    Distributed nationwide