The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56001–56025 of 73850

  • HighFDA (Devices)·Z-0496-2015·2014-12-10

    Cure Medical Recalls Pediatric Urinary Catheters Due to Labeling Error

    Cure Medical is recalling pediatric urinary catheters because some boxes are mislabeled as size 8 but contain size 10 catheters, posing a risk of injury.

    Product
    Pediatric, 10Fr, Intermittent Urinary Catheters Model: P10 Pouch Label UPC (P10) *+M405P100C* Intermediate Box Label UPC (P10) *+M405P103F* Carton Label UPC (P10) *+M405P105H* The product is distributed individually or in intermediate boxes containing 30 individual…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15712·2014-12-10

    Ethan Allen Recalls Harwood Floor Lamps Due to Electrical Shock Risk

    Ethan Allen is recalling Harwood floor lamps because a defect in the line cord insulation poses a risk of electrical shock. One incident of electrical shock has been reported.

    Product
    Harwood Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0492-2015·2014-12-10

    Ethicon Recalls PERMA-HAND Silk Suture Due to Sterility Assurance Concerns

    Ethicon is recalling PERMA-HAND silk sutures because the company cannot ensure the products meet the expected sterility assurance level.

    Product
    Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet Ethicon LLC- Made in USA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0491-2015·2014-12-10

    Integra Selector Kit Tubing Recalled for Potential Irrigation Fluid Leakage

    Integra LifeSciences is recalling 6,358 Selector Kit tubing units because they may leak irrigation fluid during use if not placed correctly on the handpiece.

    Product
    Integra Selector Kit Sterile single use device A bi-lumen, sterile single use accessory used for the Selector Integra Ultrasonic Surgical Aspirator system. One of the tubing lumen transmits irrigation fluid from the console to the handpiece of the system, and the other tubing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0486-2015·2014-12-10

    Siemens Artis zee Angiography System Software Recall

    Siemens is recalling 1,131 Artis zee and zeego Angiography Systems due to a software issue that prevents deactivating the radiation block function after a network problem.

    Product
    The Artis zee / zeego Angiography System is designed as a set of components that may be combined into different configurations to provide specialized angiography systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0487-2015·2014-12-10

    Beevers Cannulaide Model 101 Recalled for Incorrect Labeling

    Beevers Manufacturing recalled 393 units of Cannulaide Model 101 because the product was packed and labeled as Model 102.

    Product
    Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0499-2015·2014-12-10

    Amerx Health Care Recalls Amerigel Daily Dressing Packets Due to Formulation Deviation

    Amerx Health Care Corp. is recalling 1,740 units of Amerigel Daily Dressing Packets due to a formulation deviation. The affected products were distributed nationwide and internationally.

    Product
    Amerigel Daily Dressing Packets Wound management
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0288-2015·2014-12-10

    Sandoz Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Sandoz, Inc. is recalling 6,336 bottles of 16 mg candesartan cilexetil tablets because stability testing showed impurity levels exceeded specifications.

    Product
    candesartan cilexetil, tablets, 16 mg, 90-count bottles, Rx only, Manufactured for Sandoz Inc., Princeton, NJ 08540 by Mylan Laboratories Limited Hyderabad, 500 034, India, NDC 0781-5938-92
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2015·2014-12-10

    Amerx Recalls Amerigel Saturated Gauze Dressing Due to Formulation Deviation

    Amerx Health Care Corp. is recalling 21,108 units of Amerigel Saturated Gauze Dressing due to a formulation deviation. The products were distributed nationwide and internationally.

    Product
    Amerigel Saturated Gauze Dressing Wound management
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0501-2015·2014-12-10

    Microgenics Recalls MAS CardioImmune XL Cardiac Marker Control Due to Variation

    Microgenics Corporation is recalling 2,135 vials of MAS CardioImmune XL Cardiac Marker Control (Lot CXL16011) because the product shows vial-to-vial variation for specific analytes.

    Product
    MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed control serum for monitoring assay conditions in specific cardiac marker determinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0289-2015·2014-12-10

    Zydus Recalls Benzonatate Capsules Due to Foreign Capsule Contamination

    Zydus Pharmaceuticals USA is recalling Benzonatate 200 mg capsules because they may contain foreign 100 mg capsules.

    Product
    BENZONATATE Capsules, USP, 200 mg, 100 Capsule Bottles, Rx only. Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA, Inc. NDC: 68382-248-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V784000·2014-12-09

    Hyundai Recalls 2015 Sonata Vehicles Due to Axle Shaft Separation Risk

    Hyundai is recalling specific 2015 Sonata vehicles because an incorrect left axle shaft may separate from the transaxle, potentially causing the vehicle to stop moving or roll away.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E083000·2014-12-09

    Cummins Recalls Ecofit Tier2 DOC Raincaps Due to Detachment Risk

    Cummins is recalling specific Ecofit Tier2 DOC raincaps because the lid may detach, posing a crash or injury risk.

    Product
    ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:EMISSION CONTROL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15044·2014-12-09

    Lenovo Recalls Computer Power Cords Due to Fire and Burn Hazards

    Lenovo is recalling LS-15 AC power cords for laptops due to overheating risks that can cause fires and burns. Consumers should stop using the cords and contact Lenovo for a free replacement.

    Product
    AC power cords
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15711·2014-12-09

    Nordstrom Recalls Leith Open Vest Sweaters Due to Burn Hazard

    Nordstrom is recalling Leith brand open vest sweaters because they fail federal flammability standards, posing a burn injury risk. No injuries have been reported.

    Product
    Open Vest Sweaters by Leith
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15043·2014-12-09

    Dream On Me Recalls Play Yards Due to Strangulation Hazard

    Dream On Me is recalling approximately 10,000 Incredible Play Yards because the rails can collapse, posing a strangulation hazard to young children.

    Product
    Dream On Me Play Yards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V782000·2014-12-09

    Starcraft RV Recalls 2015 Launch Ultra Lite Travel Trailers for Tire Label Error

    Starcraft RV is recalling 2015 Launch Ultra Lite travel trailers because tire labels list incorrect pressure information, which could lead to over-inflation and tire blowouts.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH ULTRA LITE, redundant LAUNCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V779000·2014-12-08

    Honda Recalls 2015 Acura TLX Vehicles for Transmission Parking Defect

    Honda is recalling 2015 Acura TLX vehicles because a transmission defect may prevent the vehicle from engaging Park, increasing the risk of rolling away and crashing.

    Product
    ACURA — ACURA TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V780000·2014-12-08

    Kingmor Recalls IC CE School Buses with Cracking Wheelchair Lifts

    Kingmor is recalling 2006-2014 IC CE school buses equipped with certain Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.

    Product
    IC — IC CE
    Category
    Vehicle
    Distribution
    Distributed nationwide