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.

31201–31225 of 73745

  • ModerateFDA (Drugs)·D-0500-2020·2019-11-27

    Washington Homeopathic Recalls Natrum Muriaticum 6X Tablets for CGMP Deviations

    Washington Homeopathic Products, Inc. is recalling Natrum Muriaticum 6X Tablets because they were not manufactured under current good manufacturing practices.

    Product
    Natrum Muriaticum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64191 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2020·2019-11-27

    Conversio Health Recalls Albuterol and Ipratropium Vials Due to Processing Controls

    Conversio Health is recalling Albuterol and Ipratropium inhalation vials nationwide due to a lack of processing controls.

    Product
    Albuterol 1.25mg / Ipratropium 0.5mg, 2ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0498-2020·2019-11-27

    Washington Homeopathic Products Recalls Kali Sulphuricum 6X Tablets for CGMP Deviations

    Washington Homeopathic Products, Inc. is recalling 295 bottles of Kali Sulphuricum 6X Tablets because they were not manufactured under current good manufacturing practices.

    Product
    Kali Sulphuricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64196 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0506-2020·2019-11-27

    Washington Homeopathic Products Recalls R2103 Due to Manufacturing Deviations

    Washington Homeopathic Products, Inc. is recalling R2103 homeopathic product because it was not manufactured under current good manufacturing practices.

    Product
    R2103, Active Ingredients: Berberis Aquifolium 3x; Borax 3; , Kreosotum 10X; Sepia 3x. Inactive ingredient: 28% dilution alcohol, packaged in a) 470 mL bottle and b) 1000 mL bottle; Manufactured for Wisconsin Pharmacal Company, By: Washington Homeopathic Products, Inc., 260 JR…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0497-2020·2019-11-27

    Washington Homeopathic Products Recalls Kali Phosphoricum 6X Tablets for CGMP Deviations

    Washington Homeopathic Products, Inc. is recalling 417 bottles of Kali Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.

    Product
    Kali Phosphoricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64195 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0511-2020·2019-11-27

    Conversio Health Recalls Albuterol and Ipratropium Inhalation Vials

    Conversio Health is recalling Albuterol, Ipratropium, and Budesonide inhalation vials due to a lack of processing controls.

    Product
    Albuterol 2.5mg / Ipratropium 0.75mg /Budesonide 0.5mg, 3ML Vial, For Inhalation Only, Conversio Health, San Luis Obispo, CA 93401.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0511-2020·2019-11-27

    Neocis Guidance System Fiducial Array Recalled for Measurement Mismatch

    Neocis Inc. is recalling three units of the Neocis Guidance System Fiducial Array because they may mismatch measurement files, resulting in a failed landmark check.

    Product
    Neocis Guidance System Fiducial Array - Product Usage: The Neocis Guidance System (NGS) is a computerized navigational system intended to provide assistance in both the planning (pre-operative) and the surgical (intraoperative) phases of dental implantation surgery. The system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0502-2020·2019-11-27

    Angiodynamics Recalls BIOFLO 8F Single Titanium Non-Filled Valved Ports

    Angiodynamics Inc. is recalling BIOFLO 8F Single Titanium Non-Filled Valved ports because snap lock connectors may not meet specifications, preventing catheter insertion and delaying implantation.

    Product
    BIOFLO 8F SINGLE TITANIUM NON- FILLED; VALVED, UPN H965440250, Cat. No. 44-025 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0496-2020·2019-11-27

    Washington Homeopathic Products Recalls Kali Muriaticum 6X Tablets for CGMP Deviations

    Washington Homeopathic Products, Inc. is recalling Kali Muriaticum 6X Tablets because they were not manufactured under current good manufacturing practices.

    Product
    Kali Muriaticum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64194 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0519-2020·2019-11-27

    X-Gen Pharmaceuticals Recalls Levetiracetam Injection Due to Incorrect Package Insert

    X-Gen Pharmaceuticals is recalling Levetiracetam Injection vials because the incorrect package insert version was attached to the product.

    Product
    Levetiracetam Injection, 500 mg/5mL, 10 single-use 5 mL vials, Rx only, Manufactured by: Agile Specialties Private Limited Pilot No. 14, Sipcot II, Hosur-635 109 Tamil Nadu, India, Manufactured for: X-Gen Pharmaceuticals, Inc. Big Flats, NY 14814, NDC 39822-4000-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·20033·2019-11-26

    TJX Stores Sold 19 Recalled Products Including Infant Sleepers and Speakers

    T.J. Maxx, Marshalls, and HomeGoods sold about 1,200 units of 19 previously recalled products, including infant sleepers and speakers. Consumers should stop using these items and contact the manufacturers for remedies.

    Product
    19 different recalled products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V849000·2019-11-26

    Volvo Recalls 2011-2017 Models Due to Door Latch Defect

    Volvo is recalling 2011-2017 S60 and V60 models because a door latch component may break, potentially allowing doors to open while driving.

    Product
    VOLVO — VOLVO S60CC, S60, V60CC, V60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V853000·2019-11-26

    BMW Recalls 1999-2001 3-Series Vehicles for Driver Air Bag Inflator Defect

    BMW is recalling 1999-2001 3-Series vehicles because a replacement driver air bag inflator may absorb moisture, potentially causing it to rupture or underinflate during a crash.

    Product
    BMW — BMW 328I, 323CI, 325CI, 328CI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V852000·2019-11-26

    BMW Recalls 1999-2000 Models for Driver Air Bag Inflator Defect

    BMW is recalling 1999-2000 323i, 328i, 323Ci, and 328Ci vehicles because driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.

    Product
    BMW — BMW 323I, 328I, 328CI, 323CI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20031·2019-11-26

    Mark Feldstein Recalls Stacked Gourd Jack-O-Lanterns Due to Fire Hazard

    Mark Feldstein & Associates is recalling Stacked Gourd Jack-O-Lantern decorations because the internal wiring can overheat and ignite. Four reports of smoking or fire have been received.

    Product
    Stacked Gourd Jack-O-Lantern decorations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E080000·2019-11-26

    Takata Recalls Non-Azide Driver Air Bag Inflators for Moisture Absorption

    Takata is recalling specific non-azide driver air bag inflators used in 1995-2000 vehicles. The inflators may absorb moisture, risking rupture or underinflation during a crash.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V848000·2019-11-26

    Forest River Recalls 2020 XLR Boost Trailers Due to Axle Defect

    Forest River is recalling 2020 XLR Boost trailers because an undersized axle and tire combination may cause the trailer to be overloaded, increasing the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20710·2019-11-26

    Yamaha Recalls Portable Generators Due to Fire and Burn Hazards

    Yamaha is recalling 2018 and 2019 EF2000iS portable generators because the fuel tank can leak gasoline, posing fire and burn hazards.

    Product
    2018 and 2019 Yamaha EF2000iS portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V844000·2019-11-25

    Forest River Recalls 2018-2020 Cascade and Cherokee Travel Trailers

    Forest River is recalling 2018-2020 Cascade and Cherokee travel trailers because the trailer hitch coupler may fail, potentially causing the trailer to detach from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER CASCADE, CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V845000·2019-11-25

    Jayco Melbourne Prestige Motorhomes Recalled for Propane Tank Defect

    Jayco is recalling 2018-2020 Melbourne Prestige motorhomes because defective propane tank hangers may allow the tank to dislodge, increasing crash and fire risk.

    Product
    JAYCO — JAYCO MELBOURNE PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V846000·2019-11-25

    Entegra Recalls 2018-2020 Qwest Motorhomes for Propane Tank Defect

    Entegra is recalling 2018-2020 Qwest motorhomes because defective propane tank hangers may allow the tank to dislodge, increasing crash and fire risk.

    Product
    ENTEGRA — ENTEGRA QWEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V842000·2019-11-22

    TransTech School Buses Recalled for Roof Hatch Handle Defect

    Transportation Collaborative is recalling 2019-2020 TransTech school buses because the roof hatch handle may break, preventing emergency exit.

    Product
    TRANS TECH — TRANS TECH SST, CST
    Category
    Vehicle
    Distribution
    Distributed nationwide