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.

48601–48625 of 73840

  • HighNHTSA·16V325000·2016-05-19

    Thomas Built Buses Recalls Saf-T-Liner HDX School Buses for Hose Failure

    Daimler Trucks North America is recalling 2011-2017 Thomas Built Buses Saf-T-Liner HDX school buses because a transmission retarder may cause heater hose failure, leading to hot coolant leaks.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·042-2016·2016-05-19

    Conagra Recalls Two Beef Products Due To Undeclared Fish Allergen

    Conagra Foods is recalling two frozen beef products because they may contain undeclared fish (anchovies) from Worcestershire sauce.

    Product
    ConAgra Brands, Inc. — Conagra Foods Packaged Foods, LLC Recalls Two Beef Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V323000·2016-05-19

    Thomas Built Buses Recalls Saf-T-Liner HDX School Buses for Coolant Leak Risk

    Daimler Trucks North America is recalling 2014-2017 Thomas Built Buses Saf-T-Liner HDX school buses because a rubber coolant elbow may fail, leaking hot coolant inside the bus.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16164·2016-05-19

    Black Diamond Recalls Index Climbing Ascenders Due to Fall Hazard

    Black Diamond is recalling Index Ascenders because a rivet may release, causing the device to detach from the rope and posing a risk of injury or death.

    Product
    Black Diamond Index Ascenders for climbing
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16168·2016-05-19

    Black Diamond Recalls Camalot Climbing Devices Due to Fall Hazard

    Black Diamond is recalling approximately 45,500 Camalot and Camalot Ultralight climbing devices because they can come apart during use, posing a fall hazard.

    Product
    Black Diamond Camalot climbing devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1327-2016·2016-05-18

    Garden of Life Raw Meal Organic Vanilla Powder Recalled for Salmonella Risk

    Garden of Life is recalling Raw Meal Organic Vanilla Powder products due to possible Salmonella contamination. The recall covers multiple lot codes distributed nationwide and internationally.

    Product
    Raw Meal Organic Vanilla Powder; Organic Shake and Meal Replacement; 949 g, 475 g, and 10-ct tray (68 g each). Packaged in plastic bottle with colored label.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1328-2016·2016-05-18

    Garden of Life Organic Chocolate Powder Recalled for Salmonella Risk

    Garden of Life is recalling Raw Meal Organic Chocolate Powder products due to possible Salmonella contamination. The recall covers 422,923 units distributed nationwide and internationally.

    Product
    Raw Meal Organic Chocolate Powder; Organic Shake and Meal Replacement; 986 g, 493 g, and 10-ct tray (65 g each). Packaged in plastic bottle with colored label.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1329-2016·2016-05-18

    Garden of Life Raw Meal Organic Powder Recalled for Salmonella Risk

    Garden of Life is recalling Raw Meal Organic Original Powder products due to possible Salmonella contamination. The recall affects 422,923 units distributed nationwide and internationally.

    Product
    Raw Meal Organic Original Powder; Organic Shake and Meal Replacement; 908 g, 454 g, and 10-ct tray (65 g each). Packaged in plastic bottle with colored label.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1330-2016·2016-05-18

    Garden of Life Raw Meal Organic Vanilla Spiced Chai Powder Recalled for Salmonella

    Garden of Life is recalling Raw Meal Organic Vanilla Spiced Chai Powder due to possible Salmonella contamination. The product was distributed nationwide and in several international markets.

    Product
    Raw Meal Organic Vanilla Spiced Chai Powder; Organic Shake and Meal Replacement; 909 g, 455 g, and 10-ct tray (65 g each). Packaged in plastic bottle with colored label.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1637-2016·2016-05-18

    Bradshaw Medical Recalls Axial Torque Limiting Drivers Due to Component Failure

    Bradshaw Medical Inc. is recalling 3,760 Axial Torque Limiting Drivers because a component failure could cause applied torque to exceed the calibrated setting.

    Product
    Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw Medical Axial Torque Limiting Driver is a reusable surgical instrument designed to limit the magnitude of applied (input) torque transferred to an external (output) device or fastener in the clockwise…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1632-2016·2016-05-18

    St. Jude Medical Recalls Ellipse ICD Devices for Therapy Failure Risk

    St. Jude Medical is recalling 127 Ellipse ICD devices because they may fail to deliver high-voltage therapy needed to treat life-threatening heart rhythms.

    Product
    Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q, CD2411-36C, CD1411-36Q, CD1411-36C Product Usage: Ellipse ICD devices are intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V316000·2016-05-18

    Autocar Recalls 2016-2017 Xpeditor Vehicles Due to Rear Axle Defect

    Autocar is recalling 67 Xpeditor vehicles because improperly bent tab lock washers may allow rear axle spindle nuts to loosen, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1634-2016·2016-05-18

    Stryker Recalls CinchLock SS Knotless Anchor Due to Wire Breakage

    Stryker is recalling CinchLock SS Knotless Anchors after reports of internal wire breakage upon deployment.

    Product
    CinchLock SS Knotless Anchor with Inserter; Model number CAT02462; Orthopedic: The Pivot CinchLock SS Knotless Anchor (CAT02462) and Pivot CinchLock Flex Knotless Anchor (CAT02463) are non-degradable implant devices intended for the fixation of soft tissue to bone. Used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V319000·2016-05-18

    Autocar Recalls 2016-2017 Xpert and Xspotter Trucks for Rear Axle Defect

    Autocar is recalling 43 model year 2016-2017 Xpert and Xspotter trucks because improperly bent tab lock washers may allow rear axle spindle nuts to loosen, potentially causing the wheel assembly to separate.

    Product
    AUTOCAR — AUTOCAR XPERT, XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1616-2016·2016-05-18

    Atlas Spine Torque Limiting Handle Recalled for Implant Fracture Risk

    Atlas Spine, Inc. is recalling 16 Torque Limiting Handles because they were not appropriately set to mitigate the risk of implant fracture during rotation.

    Product
    Atlas Spine Torque Limiting Handle 6N-m, P/N 70089 Model # ITN-001-000 Used to rotate implant into position
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1666-2016·2016-05-18

    Siemens Uric Acid Assays Recalled Due to Drug Interference

    Siemens Healthcare Diagnostics is recalling Dimension Vista Uric Acid assays because NAC and Metamizole can cause falsely depressed results.

    Product
    Dimension Vista Assays: Uric Acid (URCA)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1577-2016·2016-05-18

    Medtronic Recalls Capnostream 20 Patient Monitor Battery Packs

    Medtronic is voluntarily recalling battery packs for the Capnostream 20 and 20p patient monitors because they may experience thermal runaway, posing a potential fire risk.

    Product
    Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400, 010520. Battery Pack used with the Capnostream"20 and Capnostream"20p Patient Monitor. The battery pack powers the monitor when AC power is not available or when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V318000·2016-05-18

    Heartland Recalls 2016-2017 Trailers Due to Safety Chain Failure Risk

    Heartland is recalling 2016-2017 Fair Field, Lakeview, and Resort trailers because safety chains may break if the main connection fails, increasing crash risk.

    Product
    HEARTLAND — HEARTLAND FAIR FIELD, LAKEVIEW, RESORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1635-2016·2016-05-18

    Stryker Recalls CinchLock Knotless Anchors Due to Internal Wire Breakage

    Stryker is recalling CinchLock Knotless Anchors after 13 reports of internal wire breakage upon deployment.

    Product
    CinchLock Flex Knotless Anchor with Inserter; Model number CAT02643; Orthopedic: The Pivot CinchLock SS Knotless Anchor (CAT02462) and Pivot CinchLock Flex Knotless Anchor (CAT02463) are non-degradable implant devices intended for the fixation of soft tissue to bone. Used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1325-2016·2016-05-18

    CVS Gold Emblem Organic Spiced Herbal Tea Recalled for Salmonella

    CVS Health is recalling Gold Emblem Abound Organic Spiced Herbal Tea because the product contains Salmonella. Consumers should stop using the product.

    Product
    Gold Emblem Abound Organic Spiced Herbal Tea, 20 TEA BAGS, NET WT 1.41 OZ (40g)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V315000·2016-05-18

    Lakota Luxe Trailers Recalled for Microwave Fire Risk

    Lakota is recalling 2014 Luxe trailers because the built-in microwave may start on its own, posing a fire hazard.

    Product
    LAKOTA — LAKOTA LUXE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1613-2016·2016-05-18

    Novarad NovaPACS Diagnostic Viewer Recalled for Incorrect SUV Calculations

    Novarad Corporation is recalling specific versions of NovaPACS Diagnostic Viewer because the PET/CT fusion tool calculates incorrect SUV values.

    Product
    NovaPACS  Diagnostic Viewer versions 8.3.7, 8.4.2, 8.4.3, and 8.4.4. Novarad Corporation
    Category
    Medical Device
    Distribution
    Distributed nationwide