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.

57801–57825 of 73856

  • ModerateFDA (Devices)·Z-1972-2014·2014-07-09

    Intuitive Surgical Recalls da Vinci Surgical System Quick Reference Guides

    Intuitive Surgical is recalling Quick Reference Guides for the da Vinci Surgical System to remove the Emergency Grip Release Wrench from instructions.

    Product
    IRK QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System and Si-e. Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1977-2014·2014-07-09

    BD FACS Canto Flow Cytometer Recalled for Non-Operational Cooling Fans

    BD Biosciences is recalling 35 BD FACS Canto flow cytometers and associated fluidics carts because the laser cooling fans and internal fans are not operational.

    Product
    BD FACS Canto and associated Fluidics Cart Product Usage: Flow cytometer for use in In vitro Diagnostics.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1968-2014·2014-07-09

    Intuitive Surgical Recalls da Vinci Stapler Addendum Documentation

    Intuitive Surgical is recalling documentation for the da Vinci Surgical System stapler addendum to remove references to the Emergency Grip Release Wrench.

    Product
    Stapler Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2055-2014·2014-07-09

    Physique Enhancing Science Pre-Workout Recalled for Unapproved Ingredient

    Physique Enhancing Science is recalling ENHANCED Ultra Advanced Pre-Workout supplements because they contain Aegeline, an unapproved new dietary ingredient.

    Product
    Physique Enhancing Science ENHANCED, Ultra Advanced Pre-Workout, DIETARY SUPPLEMENT Net Wt. 5.22 oz (148 g). In BlueRazz and Fruit Punch flavors
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1935-2014·2014-07-09

    Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues

    Zimmer is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.

    Product
    NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 4+. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1414-2014·2014-07-09

    West-Ward Recalls Isoniazid Tablets Due to Dissolution Failure

    West-Ward Pharmaceutical Corp. is recalling Isoniazid Tablets, USP, 300 mg because stability lots failed to meet dissolution specifications.

    Product
    Isoniazid Tablets, USP, 300 mg, Rx only, packaged in a) 100-count bottles, NDC 0143-1261-01, b) 1000-count bottles, NDC 0143-1261-10, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724; c) 30-count bottles, NDC 61748-013-30, d) 100-count bottles, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1970-2014·2014-07-09

    Intuitive Surgical Recalls Vessel Sealer QRG for da Vinci Systems

    Intuitive Surgical is recalling Vessel Sealer QRGs for da Vinci systems to remove the Emergency Grip Release Wrench from documentation.

    Product
    Vessel Sealer QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1413-2014·2014-07-09

    Baxter Recalls Brevibloc Injection Due to Particulate Matter

    Baxter Healthcare is recalling Brevibloc (esmolol hydrochloride) injection due to complaints of discolored solution and subvisible iron oxide particles.

    Product
    BREVIBLOC — BREVIBLOC (ESMOLOL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1973-2014·2014-07-09

    Intuitive Surgical Recalls Cautery QRG for da Vinci Surgical Systems

    Intuitive Surgical is recalling Cautery Quick Reference Guides for da Vinci systems to update documentation and remove a specific wrench part.

    Product
    Cautery QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1942-2014·2014-07-09

    Blue Belt Technologies Recalls Mislabeled Stride Unicondylar Knee Prosthesis Components

    Blue Belt Technologies is recalling specific lots of Stride unicondylar knee prosthesis femoral components due to packaging mislabeling that may result in the wrong implant being used.

    Product
    Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1974-2014·2014-07-09

    Intuitive Surgical Recalls da Vinci Surgical System Quick Reference Guides

    Intuitive Surgical is recalling Quick Reference Guides for the da Vinci Surgical System to remove the Emergency Grip Release Wrench from the documentation.

    Product
    Connection QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1937-2014·2014-07-09

    Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues

    Zimmer is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.

    Product
    NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 6. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1943-2014·2014-07-09

    Blue Belt Technologies Recalls Mislabeled Stride Femoral Knee Components

    Blue Belt Technologies is recalling two lots of Stride Femoral Knee Components due to packaging mislabeling that could lead to the implantation of the wrong side or size.

    Product
    Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1949-2014·2014-07-09

    DeVilbiss DV5x Series CPAP Units Recalled for Missing Serial Numbers

    DeVilbiss Healthcare LLC is recalling 1,809 DV5x Series CPAP units because they were shipped without programmed serial numbers, displaying 'RUN-TEST' on the screen.

    Product
    DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V411000·2014-07-08

    J.C. Madigan Recalls Two Ford Dump Trucks for Fire Risk

    J.C. Madigan is recalling two specific Ford dump trucks because a leaking pressure switch may cause a fire near the exhaust system.

    Product
    FORD — FORD F-550, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V408000·2014-07-07

    Genuine Scooter Recalls 2014 Stella 125 Automatic for Engine Stalling Risk

    Genuine Scooters is recalling 2014 Stella 125 Automatic scooters because a faulty engine control unit may cause the engine to stall without warning, increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER STELLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V412000·2014-07-07

    Volkswagen Recalls 2015 Golf and GTI for Steering Interference Risk

    Volkswagen is recalling 2015 Golf and GTI vehicles because loose stabilizer link fasteners may interfere with steering, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V400000·2014-07-03

    GM Recalls 5.8 Million Vehicles for Ignition Switch Airbag Risk

    General Motors is recalling 5,877,718 vehicles from 1997-2008 because the ignition switch may move out of the run position, preventing airbags from deploying in a crash.

    Product
    CHEVROLET — CHEVROLET, PONTIAC, OLDSMOBILE IMPALA, GRAND AM, GRAND PRIX, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E036000·2014-07-03

    Brake Parts Inc. Recalls Rear Wheel Brake Shoes Due to Detachment Risk

    Brake Parts Inc. is recalling specific ACDelco, Carquest, Federated, and Raybestos rear wheel brake shoes because the lining may detach from the steel shoe, potentially reducing braking force or causing wheel lockup.

    Product
    SERVICE BRAKES, AIR:DRUM:SHOES/LININGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2045-2014·2014-07-02

    Navitas Naturals Organic Sprouted Chia Powder Recalled Due to Salmonella

    Navitas Naturals is recalling Organic Sprouted Chia Powder because it is linked to a multistate outbreak of Salmonella Newport.

    Product
    Navitas Naturals Organic Sprouted Chia Powder, 8 oz (227g) package; Omega Fatty Acids, Protein, dietary Fiber. UPC 858847000369; Navitas Naturals, Novato, CA 94949
    Category
    Food
    Distribution
    Distributed nationwide