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.

44626–44650 of 73832

  • SevereFDA (Food)·F-1212-2017·2017-01-18

    All American Seasonings Recalls Jalapeno Popper Seasoning Due to Salmonella Risk

    All American Seasonings is recalling specific lots of Jalapeno Popper seasoning due to potential Salmonella contamination. Consumers should check their lot numbers and stop using the product.

    Product
    Jalapeno Popper ASI. Product Code: T3934. 33 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1201-2017·2017-01-18

    All American Seasonings Recalls Broccoli Cheese Soup Due to Salmonella Risk

    All American Seasonings is recalling 13 bags of 50 lb Broccoli Cheese Soup due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Broccoli Cheese Soup / Comfort Foods. Product Code: T3872. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1216-2017·2017-01-18

    All American Seasonings Recalls Super Nacho Seasoning Due to Salmonella Risk

    All American Seasonings is recalling 50 lb bags of Super Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Super Nacho (No-Pho, Gluten Free). Product Code: T4034. 50 lb bags.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1211-2017·2017-01-18

    All American Seasonings Recalls French Onion Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 478 bags of French Onion Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    French Onion Seasoning ASI. Product Code: T3933. 33 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1020-2017·2017-01-18

    Stryker Recalls Reunion TSA Peg Alignment Sound Due to Breakage

    Stryker Howmedica Osteonics Corp. is recalling 131 units of the Reunion TSA Peg Alignment Sound because the instrument broke during surgery.

    Product
    Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment Sound (PIN 5901-1038, Revision A) is an instrument used in the ReUnion TSA shoulder system for confirming seating height and peg alignment of the TSA Self-Pressurizing Polyethylene Glenoid implant prior to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1214-2017·2017-01-18

    All American Seasonings Recalls Triple Cheese Blend Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 59 bags of Triple Cheese Blend due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Triple Cheese Blend - No Color. Product Code: T4008. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1198-2017·2017-01-18

    All American Seasonings Recalls Buttermilk Ranch Seasoning for Salmonella Risk

    All American Seasonings, Inc. is recalling 26 boxes of Buttermilk Ranch Snack Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Buttermilk Ranch Snack Seasoning / Meat Chips. Product Code: T3760. 50 lb box
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1182-2017·2017-01-18

    FDA Recalls Broccoli Cheese Soup with Rice Due to Salmonella Risk

    Copperleaf Kitchen is recalling Country Gardens Cuisine Broccoli Cheese Soup with Rice after a supplier reported positive environmental tests for Salmonella.

    Product
    Country Gardens Cuisine, Singles, Broccoli Cheese Soup with Rice, Net Wt. 1.25 oz (35 grams)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1194-2017·2017-01-18

    All American Seasonings Recalls Non-GMO Sour Cream and Onion Seasoning

    All American Seasonings is recalling 428 bags of Non-GMO Sour Cream & Onion seasoning due to potential Salmonella contamination.

    Product
    Non-GMO Sour Cream & Onion / Deep River Snacks. Product Code: T3527. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1200-2017·2017-01-18

    All American Seasonings Recalls Kay's Naturals Cheese Puff Seasoning

    All American Seasonings is recalling 80 bags of Kay's Naturals Cheese Puff Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Cheese Puff Seasoning / Kay's Naturals. Product Code: T3852. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0987-2017·2017-01-18

    Elekta Oncentra Radiation Therapy Software Recalled for Cross Profile Defect

    Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.

    Product
    Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0430-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1007-2017·2017-01-18

    Medtronic Recalls AxIEM Touch N Go Pointer Probe for Accuracy Issues

    Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.

    Product
    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0972-2017·2017-01-18

    Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects

    Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0988-2017·2017-01-18

    ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk

    ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.

    Product
    Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1005-2017·2017-01-18

    Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard

    Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.

    Product
    FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V040000·2017-01-18

    Nissan Recalls 2015-2017 Altima Vehicles for Rear Door Latch Defect

    Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1013-2017·2017-01-18

    Beckman Coulter Recalls UniCel DxH 800 Cellular Analysis System

    Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.

    Product
    UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0965-2017·2017-01-18

    ASP Recalls EVOTECH Endoscope Cleaner Due to Hose Leak Risk

    Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.

    Product
    EVOTECH Endoscope Cleaner and Reprocessor System 208V, Product Code: 50004 The EVOTECH ECR Endoscope Cleaner and Reprocessor, a washer/disinfector, is indicated for use with high-level disinfectant CIDEX OPA Concentrate Solution and an enzymatic detergent (CIDEZYME XTRA) to…
    Category
    Medical Device
    Distribution
    Distributed nationwide