The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46601–46625 of 73832

  • HighFDA (Food)·F-2166-2016·2016-09-21

    Mars Recalls Combos Pizzeria Pretzels for Undeclared Peanut Residue

    Mars Chocolate North America is recalling Combos Pizzeria Pretzels due to potential undeclared peanut residue. The recall covers 183,678 cases distributed nationwide and abroad.

    Product
    COMBOS PIZZERIA PRETZEL - Net Wt. 6.30 Oz. (178.6 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419420065
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2117-2016·2016-09-21

    Hostess Zingers Raspberry Recalled for Unlabeled Peanut Allergen

    Hostess Brands is recalling Zingers Raspberry cakes because they were made with flour containing peanut allergen but are not labeled to contain peanuts.

    Product
    Iced Raspberry cake with creamy filling, packaged as Hostess Zingers Raspberry in 10-ct multi-packs of individual cakes, net wt. 13.40oz (360 g), UPC 888109110604; 6-ct. single serving fun size snack packs, 3 cakes per pack net wt. 4.02oz. (108g), UPC 888109010089; with the…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2782-2016·2016-09-21

    Trinity Biotech Captia Measles IgM Test Kit Recalled for QC Failure

    Clark Laboratories is recalling specific lots of the Captia Measles IgM test kit because the product failed quality control stability testing.

    Product
    Trinity Biotech Captia Measles IgM, REF/Product Code 2326060,Test Kit for 96 Determinations, IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2780-2016·2016-09-21

    Mentor Artoura Breast Tissue Expander Recall for Packaging Error

    Mentor Texas, LP. is recalling 48 Artoura Breast Tissue Expanders because CPX4 devices may have been packaged in Artoura boxes.

    Product
    Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders can be used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision and tissue defect procedures. The devices are intended for temporary subcutaneous or sub…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2781-2016·2016-09-21

    Mentor CPX4 Breast Tissue Expander Recall Due to Packaging Error

    Mentor Texas, LP. is recalling 30 units of CPX4 Breast Tissue Expanders because they may have been packaged in the wrong box.

    Product
    CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue expanders can be used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision and tissue defect procedures. The devices are intended for temporary subcutaneous or sub muscular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2777-2016·2016-09-21

    Integra Meshed Dermal Regeneration Template Recalled for Calculation Error

    Integra LifeSciences is recalling 14 packages of Meshed Dermal Regeneration Template due to an incorrect calculation of peel strength test results.

    Product
    Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 in x 2in) Rx Only Meshed Integra¿ Dermal Regeneration Template, (Integra template) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1501-2016·2016-09-21

    Amerisource Recalls bupropion Hydrochloride Tablets for Dissolution Failure

    Amerisource Health Services is recalling 2,626 bottles of bupropion hydrochloride extended-release tablets due to failed dissolution specifications.

    Product
    buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories, NDC 68001-264-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2793-2016·2016-09-21

    Siemens Syngo Plaza PACS Recall for Measurement Display Suffix

    Siemens is recalling 101 Syngo Plaza PACS systems because a suffix on DICOM images may indicate that displayed measurements differ from actual values.

    Product
    Syngo Plaza picture archiving and communication system (PAC) (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2770-2016·2016-09-21

    Sysmex Fluorocell PLT Reagent Recalled for Potential Low Platelet Results

    Sysmex America Inc is recalling Fluorocell PLT reagent because it may produce falsely low platelet results on Sysmex XN-Series analyzers.

    Product
    Fluorocell PLT reagent, Catalog #CD994563 Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2794-2016·2016-09-21

    Siemens Syngo.Plaza VB 10 A PACS Recall for Measurement Suffix Display

    Siemens is recalling 101 Syngo.Plaza VB 10 A image processing systems because a suffix on DICOM images may indicate that displayed measurement values differ from real values.

    Product
    Syngo.Plaza VB 10 A, image processing system (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2804-2016·2016-09-21

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Calibrator Kit 31

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 31, Lot 3155, because an incorrect value on the Assay Data Disks prevents successful calibration of the HbA1c assay.

    Product
    The VITROS¿ Chemistry Products Calibrator Kit 31, Lot 3155 used in conjunction with: VITROS¿ Chemistry Products HbA1c Reagent Kit, Generation 6 (GEN 6) and Assay Data Disk (ADD), Data Release Versions (DRV) 5873, 5874, 5875, or 5876, is used to calibrate the VITROS 5,1 FS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2779-2016·2016-09-21

    Biomerieux Recalls VIDAS NT-pro-BNP Kits Due to Packaging Error

    Biomerieux is recalling 229 VIDAS NT-pro-BNP kits because they contain the incorrect number of control vials.

    Product
    VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2778-2016·2016-09-21

    Alere LDX Optical Check Cassettes Recalled for Incorrect Expiration Date

    Alere San Diego, Inc. is recalling LDX Optical Check Cassettes because the expiration date on the magnetic strip does not match the labeled date.

    Product
    LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Cassette in box with foam insert. The cassette is used to check the optics system of the LDX analyzer. Product Usage: The Optics Check Cassette is used to check the optics system of the Alere Cholestech…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V678000·2016-09-20

    New Flyer Recalls 2016 XN60 and XN40 Buses for CNG Defect

    New Flyer is recalling 38 model year 2016 XN60 and XN40 transit buses because a pressure relief device may fracture, releasing high-pressure gas and increasing fire risk.

    Product
    NEW FLYER — NEW FLYER XN60, XN40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V679000·2016-09-20

    Ducati Recalls XDiavel Motorcycles for Loose Final Drive Pulley Nut

    Ducati is recalling 2016-2017 XDiavel motorcycles because a loose final drive pulley nut may cause loss of power to the rear wheel, increasing crash risk.

    Product
    DUCATI — DUCATI XDIAVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E073000·2016-09-20

    Porsche Brake Fluid Recall Due to Missing DOT 4 Labeling

    Porsche is recalling specific 1L and 30L brake fluid containers manufactured between September 2015 and August 2016 because they lack the required 'DOT 4' label, posing a risk of incompatible fluid use.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V680000·2016-09-20

    Porsche Recalls 2017 Macan Models Due to Front Suspension Defect

    Porsche is recalling 2017 Macan models because front anti-rollbar links may move out of position, causing oversteer and increasing crash risk.

    Product
    PORSCHE — PORSCHE MACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16267·2016-09-20

    Denon Recalls HEOS 1 Go Pack Battery Packs for Fire and Burn Hazards

    Denon is recalling HEOS 1 Go Pack rechargeable battery packs because they can overheat, posing fire and burn hazards. No injuries have been reported.

    Product
    HEOS 1 Go Pack rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V675000·2016-09-19

    Mitsubishi Recalls 2017 Mirage Vehicles for Headlight Adjustment Defect

    Mitsubishi is recalling 2017 Mirage vehicles with HID headlamps because the horizontal adjustment clips may not be secured, potentially reducing visibility or blinding oncoming drivers.

    Product
    MITSUBISHI — MITSUBISHI MIRAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·083-2016·2016-09-17

    Gallo Meats Recalls Sausage, Beef, and Lamb Products Lacking Federal Inspection

    Gallo Meats LLC is recalling approximately 82 pounds of sausage, beef, and lamb products produced without federal inspection. The hot Italian sausage may also contain undeclared allergens.

    Product
    Gallo Meats LLC. Recalls Sausage, Beef and Lamb Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·081-2016·2016-09-16

    Tucson Tamale Wholesale Recalls Beef Tamales Lacking Federal Inspection

    Tucson Tamale Wholesale Company is recalling 915 pounds of beef tamales because the meat was produced without federal inspection. No illnesses have been reported.

    Product
    Tucson Tamale Wholesale Company LLC — Tucson Tamale Wholesale Company, LLC Recalls Beef Tamale Products Containing Meat Produced Without Benefit of Federal Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V672000·2016-09-16

    Toyota Recalls 2016 Prius Vehicles Due to Air Bag Inflation Error

    Toyota is recalling 7,817 model year 2016 Prius vehicles because a manufacturing error may cause the front passenger air bag to partially inflate unintentionally.

    Product
    TOYOTA — TOYOTA PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V671000·2016-09-16

    Jayco Recalls 2017 Octane Travel Trailers for Incorrect Tire Labels

    Jayco is recalling 2017 Octane Super Lite travel trailers because incorrect tire labels may lead to over-inflation and sudden tire failure.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER OCTANE
    Category
    Vehicle
    Distribution
    Distributed nationwide