The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32876–32900 of 73745

  • ModerateFDA (Drugs)·D-1496-2019·2019-07-31

    Pharma-Natural Recalls Army Health Pain Reliever Gel Due to CGMP Violations

    Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.

    Product
    ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%), 0.5 OZ jar, Manufactured exclusively for: Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00461 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2061-2019·2019-07-31

    Medela Breast Milk Transfer Lid Recall for Packaging Sterility Concerns

    Medela Inc is recalling 665,600 breast milk transfer lids because packaging breaches may compromise sterility, even if the packaging appears intact.

    Product
    Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2063-2019·2019-07-31

    Merge OrthoPACS Software Recalled for Image Display Ordering Issues

    Merge Healthcare is recalling 73 units of Merge OrthoPACS software due to potential display errors in image ordering and scrolling.

    Product
    Merge OrthoPACS versions 7.3, 7.3.1, 8.0 and 8.0.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2018-2019·2019-07-31

    Siemens AXIOM Artis TA X-ray Generator Recall for Power Supply Issue

    Siemens is recalling five AXIOM Artis TA units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.

    Product
    AXIOM Artis TA, Model Number 7007755
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2015-2019·2019-07-31

    Siemens AXIOM Artis BC X-ray Generator Recall Due to Power Supply Issue

    Siemens is recalling six AXIOM Artis BC units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.

    Product
    AXIOM Artis BC, Model Number 5904649
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1500-2019·2019-07-31

    FDA Recalls Dermanak Skin Cream Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling Dermanak Skin Fade Cream because it was manufactured with current good manufacturing practice violations.

    Product
    Dermanak original crema blanqueador (Hydroquinone 2%) Skin Fade Cream, 2 OZ. (56.7 g) jar, Manufactured by: Pamby Distributors, Inc., Miami, FL 33126, NDC 63788-108-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2027-2019·2019-07-31

    Siemens AXIOM Artis dBC X-ray Generator Recall for Power Supply Defect

    Siemens is recalling 53 AXIOM Artis dBC units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.

    Product
    AXIOM Artis dBC, Model Number 7728392
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2021-2019·2019-07-31

    Siemens AXIOM Artis dTC X-ray Generator Recall for Power Supply Defect

    Siemens is recalling 98 AXIOM Artis dTC units because a power supply tolerance issue may cause generator failure, preventing X-ray imaging.

    Product
    AXIOM Artis dTC, Model Number 7413078
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2079-2019·2019-07-31

    Abbott Recalls ARCHITECT BNP Controls Due to Stability Drift

    Abbott Laboratories is recalling ARCHITECT BNP Controls because of a time-dependent stability drift that affects test results.

    Product
    ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are for the estimation of test precision and the detection of systematic analytical deviations of the ARCHITECT iSystem (reagents, calibrators and instrument), when used for the quantitative determination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1518-2019·2019-07-31

    Lupin Recalls Nystatin and Triamcinolone Acetonide Cream for Stability Failure

    Lupin Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream due to a failed uniformity of containers test. The recall covers 33,939 tubes distributed nationwide.

    Product
    NYSTATIN AND TRIAMCINOLONE ACETONIDE — NYSTATIN AND TRIAMCINOLONE ACETONIDE (NYSTATIN AND TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V558000·2019-07-29

    Mazda Recalls 2019 Mazda3 Vehicles for Rearview Mirror Defect

    Mazda is recalling 2019 Mazda3 vehicles with manual dimming mirrors because the mirror may detach, reducing rearward visibility and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V557000·2019-07-26

    Temsa Recalls 2014-2019 TS45 Buses for Steering Hose Defect

    Temsa is recalling 2014-2019 TS45 buses because hydraulic steering hoses may leak or burst, potentially affecting steering ability and increasing crash risk.

    Product
    TEMSA — TEMSA TS45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V561000·2019-07-26

    Moto Guzzi and Aprilia Motorcycles Recalled for Front Brake Master Cylinder Defect

    Piaggio is recalling specific Moto Guzzi and Aprilia motorcycles because a front brake master cylinder defect may cause unexpected slowing or stopping without warning to following traffic.

    Product
    MOTO GUZZI — MOTO GUZZI, APRILIA CALIFORNIA, DORSODURO, ELDORADO, AUDACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V556000·2019-07-26

    Chrysler Recalls 2019 Ram 1500 for Instrument Cluster Illumination Defect

    Chrysler is recalling 2019 Ram 1500 vehicles because the instrument cluster may fail to illuminate driver warnings, increasing crash risk. Dealers will replace the cluster free of charge.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19764·2019-07-26

    Spansive Recalls Wireless Phone Chargers Due To Burn Hazard

    Spansive is recalling about 950 wireless multi-phone chargers sold in May 2019 because metallic accessories can overheat, posing a burn hazard.

    Product
    Spansive Source wireless, multi-phone chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V555000·2019-07-26

    Starcraft Bus Recalls 2018-2019 Models Due to Roof Hatch Handle Defect

    Forest River is recalling 2018-2019 Starcraft Allstar, Allstar XL, and Starlite vehicles because the roof hatch external handle may break, preventing emergency egress.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALLSTAR, STARLITE, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·19175·2019-07-25

    Cannondale CAADX Bicycles Recalled Due to Fork Breakage and Fatality Risk

    Cycling Sports Group is recalling 2013-2016 Cannondale CAADX bicycles because the fork can break, posing a fall hazard. One fatality and seven serious injuries have been reported.

    Product
    2013 through 2016 Cannondale CAADX cyclocross bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19763·2019-07-25

    Britax Recalls Modified Thru-Bolt Axles for BOB Jogging Strollers

    Britax is recalling modified thru-bolt axles for BOB jogging strollers because the front wheel can fracture and detach, posing fall and injury hazards.

    Product
    Modified thru-bolt axles for use with BOB Jogging Strollers distributed through the BOB Information Campaign from January 10, 2019 to April 26, 2019
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19174·2019-07-25

    Stokke Recalls Steps Bouncers Due to Fall Hazard

    Stokke is recalling Steps Bouncers because they can detach from the Steps Chair, posing a fall hazard to infants.

    Product
    Stokke® Steps™ Bouncers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V550000·2019-07-25

    Thomas Built Buses Recalling School Buses for Roof Hatch Handle Defect

    Daimler Trucks North America is recalling 2019-2020 Thomas Built school buses because the roof escape hatch handle may break, hindering emergency egress.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, MINOTOUR, SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide