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.

57751–57775 of 73856

  • HighNHTSA·14E040000·2014-07-14

    PACCAR Recalls Mirrex and TRP Warning Triangle Kits for Missing Markings

    PACCAR is recalling aftermarket Mirrex and TRP warning triangle kits sold between 2009 and 2014 because they lack required manufacturer markings, failing to meet federal safety standards.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V422000·2014-07-14

    BMW Recalls 2014 i3 and MINI Cooper for Air Bag Defect

    BMW is recalling certain 2014 i3 and MINI Cooper vehicles because the front passenger air bag inflator may not be assembled correctly, potentially preventing proper deployment in a crash.

    Product
    BMW — BMW, MINI I3, COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E038000·2014-07-11

    Tucker Rocky Recalls Cyber River Road Grateful Dead U-6 Motorcycle Helmets

    Tucker Rocky is recalling specific Cyber River Road Grateful Dead U-6 motorcycle helmets because they failed federal safety impact tests. Owners should contact the company for a free replacement.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E037000·2014-07-10

    Airtex E84070 Replacement Fuel Pumps Recalled for Leak Risk

    UCI-Fram Group is recalling Airtex E84070 replacement fuel pumps shipped between December 2013 and June 2014 due to a seal defect that may cause fluid leaks and increase fire risk.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14228·2014-07-10

    Gemini Recalls Power Adaptor Chargers Due to Burn Hazard

    Gemini is recalling about 31,000 promotional power adaptors/chargers because they can overheat and cause burns. Consumers should stop using and dispose of the units.

    Product
    Power adaptor/chargers (promotional giveaway)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V419000·2014-07-10

    Nissan Recalls 2014 NV Vans Due to Seat Belt Bolt Defect

    Nissan is recalling 2014 NV vans because seat belt retractor bolts may be loose or missing, potentially compromising occupant restraint in a crash.

    Product
    NISSAN — NISSAN NV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V426000·2014-07-10

    Roush Recalls 2010-2012 Ford E-Series Vans Due to Propane Leak Risk

    Roush is recalling 2010-2012 Ford E-Series vans with specific propane conversion kits due to a potential fuel leak that could cause a fire.

    Product
    FORD — FORD E-250, E-350, E-150, E-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14226·2014-07-10

    Lifeguard Press Recalls Charging Kits Due to Fire and Shock Hazards

    Lifeguard Press is recalling about 25,400 charging kits sold at Dillard's, Lilly Pulitzer, and Nordstrom's because the wall chargers can overheat, spark, or detach prongs, posing fire and shock risks.

    Product
    Charging Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1978-2014·2014-07-09

    Stryker Triathlon Patella Inserter Recalled for Instrument Fracture Risk

    Stryker Howmedica Osteonics is recalling 22 units of the Triathlon Tritanium Patella Inserter because the instrument may fracture during implantation.

    Product
    Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the Tritanium Knee System Instrument Set. It is used to implant the Tritanium Patella after the patellar bone has been prepared using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1985-2014·2014-07-09

    Siemens Mobilett XP X-ray System Recalled for Fire Hazard

    Siemens is recalling 10 Mobilett XP Digital Mobile X-ray Systems due to a potential fire hazard from Lithium-Ion batteries installed between October 2010 and April 2011.

    Product
    Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Mobilett XP and Mobilett XP Hybrid are radiographic systems designed for use in wards, intensive care, and premature birth-wards, pediatric and emergency departments, operating theatres as well as the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1948-2014·2014-07-09

    Ventlab Manual Resuscitator Bags Recalled Due to Valve Defect

    Ventlab LLC is recalling 251,384 manual resuscitator bags because a defective pop-off valve may prevent air delivery during emergency resuscitation.

    Product
    Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT5000, BVM700, CPRM1000, CPRM2000, CPRM3000, PRO-1900, PRO-1000, PRO-2000, SC7000, SC8000, SC8020, SC8120, SC9000, SS3200, VN2000, VN3000, VN4000, VN5000, VT1000 , VN2102, VN2002.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1991-2014·2014-07-09

    Siemens Recalls ADVIA Centaur TnI-Ultra Assay Kits Due to Reagent Appearance

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur TnI-Ultra assay kits because a darker solid phase reagent in some lots may lead to incorrect test results.

    Product
    ADVIA Centaur¿ Systems TnI-Ultra assay; Catalog Number 02789602 (100 tests), SMN 10317708 and 02790309 (500 tests), SMN 10317790
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1981-2014·2014-07-09

    Vascular Solutions Recalls Langston Dual Lumen Catheters Due to Separation Risk

    Vascular Solutions is recalling Langston Dual Lumen Catheters because the inner catheter may separate from the hub during use, potentially requiring intervention to prevent injury.

    Product
    Langston Dual Lumen Catheters, 6Fr, REF 5550 and 5540. The Vascular Solutions Langston Dual Lumen Pressure Monitoring catheter is used as a pressure measurement catheter and for delivery of contrast media during angiographic studies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2077-2014·2014-07-09

    Olde Thompson Recalls Kirkland Signature Coarse Ground Malabar Black Pepper

    Olde Thompson is recalling Kirkland Signature Coarse Ground Malabar Black Pepper due to potential Salmonella contamination. The product was distributed nationwide in the US and in Canada.

    Product
    Kirkland Signature Coarse Ground Malabar Pepper, 12.7 oz Plastic Jars, UPC 096619164998. Packaging includes a PET bottle. The lid is made of Polypropylene and contains a tinplate insert and a Polypropylene five-hole cap. The label on the jar is a rectangular label (front and…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1931-2014·2014-07-09

    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 1. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1944-2014·2014-07-09

    Siemens syngo Lab Data Manager Software Recall for Configuration Errors

    Siemens is recalling syngo Lab Data Manager software because configuration errors may cause test results to bypass manual review and release to the Laboratory Information System.

    Product
    syngo Lab Data Manager, SMN 10800057, 10803189, and 10804573.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1947-2014·2014-07-09

    Alcon Anterior Chamber Cannula Recall Due to Incorrect Component

    Alcon is recalling CUSTOM-PAKs that contain a sharp tip needle instead of the intended anterior chamber cannula.

    Product
    Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part Number 585006 contained in Alcon Assembly Numbers 9795-37, 11233-14, and 13334-04. The product is typically inserted through an incision during cataract surgery to deliver balanced salt solution to help…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1963-2014·2014-07-09

    Baxter Exactamix Compounder Recall Due to Software Configuration Error

    Baxter Healthcare is recalling Exactamix 1200 and 2400 Compounders because a software error may prevent pump tube flushing, risking cross-contamination of IV solutions.

    Product
    EXACTAMIX 1200 Compounder, model numbers 1200-DY, 1200-DX, 1200-DYR and 1200-DXR; EM1200 DY Display, Replacement EM 1200 DY Display. EXACTAMIX 2400 Compounder model numbers 2400-DY, 2400-DX, 2400-DYR and 2400-DYX. Baxa Corporation. An automated pumping system that compounds…
    Category
    Medical Device
    Distribution
    Distributed nationwide