The Recall Desk

State

Northern Mariana Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39051–39075 of 73764

  • ModerateFDA (Devices)·Z-1164-2018·2018-03-28

    Arrow Central Venous Catheter Kits Recalled for Missing Clinical Documentation

    Arrow International is recalling 18,124 central venous catheter kits because they lack required clinical guidance documents. The recall is nationwide.

    Product
    Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Permits venous access to central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1158-2018·2018-03-28

    Arrow International Recalls Percutaneous Sheath Introducer Kits Missing Safety Checklists

    Arrow International is recalling 18,124 percutaneous sheath introducer kits because they lack required central line insertion checklists and procedure notes.

    Product
    Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1159-2018·2018-03-28

    Arrow Central Venous Catheter Kits Recalled for Missing Clinical Guidance Documents

    Arrow International is recalling 18,124 central venous catheterization kits because they are missing the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.

    Product
    Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access and catheter introduction to the central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1163-2018·2018-03-28

    Arrow Central Venous Catheter Kits Recalled for Missing Safety Checklists

    Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required procedural notes and insertion checklists.

    Product
    Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access to central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1147-2018·2018-03-28

    Ethicon Recalls DERMABOND PRINEO Skin Closure System Lots

    Ethicon is recalling specific lots of the DERMABOND PRINEO Skin Closure System because the adhesive may not dry within the specified time and may fall off.

    Product
    DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO System is intended for topical application only to hold closed easily approximated skin edges of wounds from surgical incisions, including punctures from minimally invasive surgery, and simple…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1131-2018·2018-03-28

    CooperSurgical 2 MHz Waterproof OB Probe Recalled for Mislabeling

    CooperSurgical is recalling 13 units of 2 MHz Waterproof OB probes because they were incorrectly labeled as 3 MHz probes.

    Product
    Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical 2 MHz Waterproof OB probe is for obstetrical use in the labor and department for late term obstetrical examination associated with larger women. The product detects fetal heart beats as an aid for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1160-2018·2018-03-28

    Arrow International Recalls Percutaneous Sheath Introducer Kits Missing Safety Checklists

    Arrow International is recalling 18,124 percutaneous sheath introducer kits because they are missing the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.

    Product
    Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1162-2018·2018-03-28

    Arrow Central Venous Catheter Kits Recalled for Missing Safety Checklists

    Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required clinical safety checklists.

    Product
    Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Permits venous access to central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0617-2018·2018-03-28

    Akorn Recalls Triamcinolone Acetonide Lotion Due to Impurity Levels

    Akorn, Inc. is recalling 4,128 bottles of Triamcinolone Acetonide Lotion, USP 0.1% due to high impurity levels. The product was distributed nationwide and in Puerto Rico.

    Product
    Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V198000·2018-03-27

    Newmar Recalls Motorhomes Due to Power Steering Hose Routing Defect

    Newmar is recalling 2011-2017 Mountain Aire, Dutch Star, and Ventana motorhomes because the power steering hose may rub against the starter motor, causing fluid leaks or electrical arcing.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V191000·2018-03-26

    Western Star Trucks Recalled for Electrical Arc Fire Risk

    Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc that increases fire risk.

    Product
    WESTERN STAR — WESTERN STAR 6900, 4900, 4700, 5700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V192000·2018-03-26

    Thomas Built Buses Recall School Buses Due to Seat Bracket Crack Risk

    Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, causing seats to detach in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, MINOTOUR, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V190000·2018-03-26

    Thomas Built Buses Saf-T-Liner C2 Propane Leak Recall

    Daimler Trucks North America is recalling 2014-2019 Thomas Built Buses Saf-T-Liner C2 school buses with propane engines due to a fuel line chafing risk that could cause a leak and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V193000·2018-03-26

    Thomas Built Buses Recall Transit Models Due to Seat Bracket Defect

    Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses transit models because a wall mounting bracket may crack, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V194000·2018-03-26

    Daimler Trucks Recalls 2018-2019 Freightliner Custom Chassis XCS Vehicles

    Daimler Trucks North America is recalling 2018-2019 Freightliner Custom Chassis XCS motorhome chassis because a valve stem stabilizer may dislodge, potentially causing tire damage and increasing crash risk.

    Product
    FCCC — FCCC XCS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V188000·2018-03-23

    Ferrari Recalls 458 Italia and California Models for Air Bag Defect

    Ferrari is recalling 2009-2011 California and 2010-2011 458 Italia vehicles because passenger air bag inflators may explode during a crash, posing a risk of serious injury or death.

    Product
    FERRARI — FERRARI 458 ITALIA, CALIFORNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V197000·2018-03-23

    Lazy Daze Recalls Motorhomes with Defective Fire Extinguishers

    Lazy Daze is recalling 2012-2017 motorhomes because certain fire extinguishers may clog or detach, potentially failing to work during a fire.

    Product
    LAZY DAZE — LAZY DAZE 27' MID-BATH (27MB), 27' REAR BATH (27RB), 24' FRONT DINETTE(24FD), 27' REAR KITCHEN (27RK)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18129·2018-03-22

    SpeeCo and Woods Recall 4-Way Wedge Accessory for Log Splitters

    SpeeCo and Woods are recalling 4-way wedge accessories for hydraulic log splitters because they can detach and strike users, causing injury.

    Product
    4-way wedge accessory for hydraulic log splitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0596-2018·2018-03-21

    Pfizer Recalls Hydromorphone Hydrochloride Injection Due to Non-Sterility Concerns

    Pfizer is recalling 53,600 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass vials.

    Product
    HYDROMORPHONE HYDROCHLORIDE — HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0984-2018·2018-03-21

    Alden Optical Recalls HP49 Sphere Daily Wear Soft Contact Lenses

    Alden Optical is recalling 23 units of HP49 Sphere Daily Wear Soft contact lenses because they lack sterility assurance.

    Product
    Alden HP49 Sphere Daily Wear Soft contact; Catalog Number: AOHPS49 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or…
    Category
    Medical Device
    Distribution
    Distributed nationwide