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.

49651–49675 of 73840

  • ModerateFDA (Devices)·Z-1038-2016·2016-03-09

    Stryker AccuPlace Round Level Needle Guide Recalled for Sterility Breach Risk

    Stryker is recalling AccuPlace Round Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.

    Product
    (Stryker) AccuPlace Round Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1041-2016·2016-03-09

    Volcano R-100 Sterile Equipment Covers Recalled for Incorrect Expiry Date Labeling

    Volcano Corporation is recalling R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.

    Product
    Volcano R100 Sterile Equipment Cover; Sterile; General Hospital: These Sterile Equipment covers are provided to cover equipment that is mean to be used in the sterile surgical field but cannot be sterilized. The sterile drapes are put over this equipment in case any sterile…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1037-2016·2016-03-09

    Stryker AccuPlace Needle Guide Recalled for Sterility Breach Risk

    Stryker is recalling AccuPlace Straight Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.

    Product
    (Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1036-2016·2016-03-09

    Medical Action Industries Recalls PICC/CVC Dressing Kits Due to Misbranding

    Medical Action Industries is recalling 180 PICC/CVC Secure Dressing Change kits because the presence of CHG is not identified on the exterior labeling.

    Product
    PICC/CVC Secure Dressing Change kit, Ref: 73775, Lot 213403, Sterile Single Use, Medical Action Industries, Inc., Arden, NC. This kit is used by clinicians to change dressings
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1040-2016·2016-03-09

    Stryker AccuPlace Drace Stereotaxic Needle Guide Recalled for Sterility Risk

    Stryker is recalling 5,800 AccuPlace Drace Stereotaxic Needle Guides due to a potential breach in sterility caused by packaging damage.

    Product
    50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2016·2016-03-09

    Volcano Sterile Equipment Covers Recalled for Incorrect Expiry Date Labeling

    Volcano Corporation is recalling certain lots of R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.

    Product
    Volcano SpinVision Sterile Equip cover II; Sterile; General Hospital: These Sterile Equipment covers are provided to cover equipment that is mean to be used in the sterile surgical field but cannot be sterilized. The sterile drapes are put over this equipment in case any…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1019-2016·2016-03-09

    Virage OCT Spinal Fixation System Recall for Updated Surgical Guidance

    Zimmer Spine is issuing a Class II correction for the Virage OCT Spinal Fixation System to provide additional guidance in the surgical technique manual.

    Product
    Virage OCT Spinal Fixation System. Intended to promote fusion of the Occipital-Cervical-Thoracic spine (Occiput-T3).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0734-2016·2016-03-09

    J. Strickland Recalls Subpotent Sulfur8 Anti-Dandruff Conditioner

    J. Strickland and Co is recalling Sulfur8 Medicated Light Formula anti-dandruff conditioner because it failed stability testing. The product is subpotent.

    Product
    sulfur8 medicated LIGHT FORMULA (sulfur) anti-dandruff hair & scalp conditioner, 2%, packaged in a) 2 OZ (57g) jar (UPC 0 75610 43510 8), and b) 4 OZ (113g) jar (UPC 0 75610 43610 5), 1 dozen jars per case, J. Strickland & Co., PO Box 1637, Olive Branch, MS 38654
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V142000·2016-03-08

    Setra Recalls 2005-2009 S417 Coaches Due to Control Arm Defect

    Setra is recalling 2005-2009 S417 coaches because a cracked control arm tube can separate, potentially causing loss of vehicle control and increasing crash risk.

    Product
    SETRA — SETRA S417
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V139000·2016-03-07

    Thor Motor Coach Recalls 2014-2016 Hurricane and Windsport Motor Homes

    Thor Motor Coach is recalling 385 model year 2014-2016 Hurricane and Windsport motor homes because heat from the exhaust system may cause a storage compartment to melt, increasing the risk of fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E018000·2016-03-07

    ZF Front Control Arm Recall Due to Potential Tube Separation

    ZF Group is recalling specific front control arms where a manufacturing defect may cause the tube to separate from the shaft, potentially leading to loss of vehicle control.

    Product
    SUSPENSION:FRONT:CONTROL ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V138000·2016-03-07

    Volkswagen Recalls 2015-2016 e-Golf Vehicles for Battery Software Defect

    Volkswagen is recalling 2015-2016 e-Golf vehicles because oversensitive battery diagnostics may cause the electric motor to shut down unexpectedly, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN E-GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-030716·2016-03-07

    Yummy Chicken Breast Nuggets Recalled for Metal Contamination

    USDA FSIS issued a public health alert for Yummy brand chicken nuggets potentially contaminated with metal pieces. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert For Imported Chicken Product For Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V137000·2016-03-07

    Jaguar Recalls 2013-2015 XF Vehicles for Power Steering Defect

    Jaguar is recalling 2013-2015 XF vehicles because a faulty engine component may cause a loss of power steering assist, increasing crash risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V131000·2016-03-04

    Prevost Recalls X3-45 Buses Due to Cracking Passenger Seat Frames

    Prevost is recalling 2015-2016 X3-45 buses because cracks in sliding passenger seats may compromise structural integrity, increasing injury risk in crashes.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V133000·2016-03-04

    Prevost Recalls Coaches Due to Fuel Line Fire Risk

    Prevost is recalling specific 2011-2016 coach models because a missing clip allows the coolant line to rub against the fuel hose, potentially causing a fuel leak and engine compartment fire.

    Product
    PREVOST — PREVOST H3-41, H3-45, H3-VIP, X3-VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V136000·2016-03-04

    Club Car Precedent Golf Carts Recalled for Missing Safety Equipment

    Hardkore Karts is recalling 2009-2013 Club Car Precedent golf carts with street packages that lack required VINs, certification labels, and DOT-compliant windshields.

    Product
    CLUB CAR — CLUB CAR PRECEDENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V135000·2016-03-04

    Nova Bus Recalls 2014-2016 LFS Models for Wiper Arm Defect

    Nova Bus is recalling 863 LFS and LFS Artic buses from 2014-2016 because a wiper idler arm pin may strip, causing wipers to stop working and reducing visibility.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V132000·2016-03-04

    Haulmark Motorcoach Recall for Unstable Entry Steps

    Universal Trailer is recalling 2007-2010 Haulmark Motorcoaches because a bolt may fracture, causing entry steps to become unstable and increasing injury risk.

    Product
    HAULMARK — HAULMARK MOTORCOACH
    Category
    Vehicle
    Distribution
    Distributed nationwide