The Recall Desk

State

Northern Mariana Islands product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19751–19775 of 73399

  • ModerateCPSC·22188·2022-07-21

    Baby Mirror Activity Toys Recalled for Sharp Mirror Laceration Hazard

    Konges Sløjd Baby Mirror Activity Toys are being recalled because the mirror can detach from the silicone cover, exposing sharp edges that pose a laceration risk to children. About 85 units were sold in the United States.

    Product
    Baby Mirror Activity Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2022·2022-07-20

    Knorr Curry Chicken and Rice Soup Mix Recalled for Undeclared Milk

    MSI Express Inc. is recalling Knorr Curry Chicken and Rice Soup Mix because it contains undeclared milk, a known allergen.

    Product
    MSI Express Inc. Recalls Unilever Food Solutions U.S. Knorr Curry Chicken and Rice Soup Mix Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1428-2022·2022-07-20

    Natreve Vegan Protein Powder Recalled for Undeclared Milk Allergen

    Natreve Vegan Protein Powder (Lot# 46359 and 46360) is recalled nationwide due to an undeclared milk allergen.

    Product
    Natreve Vegan Protein Powder 10 servings, 13.1oz (371g), UPC 628831120003 18 servings, 1.47lbs/23.53oz (667g), UPC 628831110073
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1284-2022·2022-07-20

    Arti King tablets recalled for undeclared pharmaceutical ingredients

    Arti King Refozado con Ortiga y Omega 3 Tablets are recalled nationwide because FDA testing found undeclared diclofenac and dexamethasone. The product was marketed without FDA approval and should not be used.

    Product
    Arti King Refozado con Ortiga y Omega 3 Tablets, 100-count bottles, Hecho en Mexico por: "PLANTAS MEDICINALES DE MEXICO", Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800 Mexico, UPC 7 501031 111138
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1196-2022·2022-07-20

    BCAA Injection Vials Recalled for Lack of Sterility Assurance

    Tailor Made Compounding is recalling 180 vials of BCAA (branched-chain amino acid) injections nationwide due to inability to assure the product maintained sterility. Affected batches expire between April and June 2022.

    Product
    BCAAs (Leucine/Iso-Leucine/Valine) 10mg/10mg/5mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V516000·2022-07-20

    Audi Q8 and Q7 Fuel Pump Failure Risk Recall

    Volkswagen is recalling certain 2019-2021 Audi Q8 and 2020-2021 Audi Q7 vehicles due to a fuel pump component that may break, causing the pump to fail. A failed fuel pump can stall the engine, increasing crash risk.

    Product
    AUDI — AUDI Q7, Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1197-2022·2022-07-20

    Biotin 5mg/mL injection recalled for lack of sterility assurance

    Tailor Made Compounding is recalling Biotin 5mg/mL injections distributed nationwide and in Puerto Rico because the manufacturer cannot assure the products were sterilized according to FDA standards.

    Product
    Biotin 5mg/mL, 5mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1195-2022·2022-07-20

    Ascorbic Acid Injectable Vials Recalled Due to Sterility Assurance Failure

    Tailor Made Compounding is recalling ascorbic acid injectable vials due to lack of sterility assurance. The affected vials were distributed nationwide and in Puerto Rico.

    Product
    Ascorbic Acid 500mg/mL, a) 25 ml-vial, b) 50 ml-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1239-2022·2022-07-20

    Testosterone Propionate Injectable Vials Recalled Over Sterility Assurance

    Testosterone propionate injectable vials are being recalled due to lack of assurance of sterility. The recall affects product distributed nationwide in the USA and Puerto Rico.

    Product
    Testosterone Propionate 100mg/ml, 10mL-vial, Room temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1238-2022·2022-07-20

    Compounded Testosterone Enanthate Injectables Recalled for Lack of Sterility Assurance

    Tailor Made Compounding is recalling 414 vials of Testosterone Enanthate 200mg/ml (5 mL and 10 mL) due to lack of assurance of sterility. The product was distributed nationwide in the USA and Puerto Rico.

    Product
    Testosterone Enanthate (GSO) 200mg/ml, a) 5 mL-vial, b) 10 mL-vial, Room temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1214-2022·2022-07-20

    Compounded Injectable Medication Recalled for Lack of Sterility Assurance

    Tailor Made Compounding is recalling 232 vials of Methionine/Inositol/Choline B12 injectable across the U.S. and Puerto Rico due to lack of assurance of sterility. Patients who received this medication should contact their healthcare provider.

    Product
    Methionine/Inositol/Choline B12 25mg/50mg/50mg/1mg/mL, a)10 mL-vial, b) 30 mL-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1189-2022·2022-07-20

    Drug Recall: Draximage MAA Injectable Kit Due to Sterility Failure

    Jubilant Draximage Inc. is recalling Draximage MAA, an injectable diagnostic drug kit, due to failed endotoxin testing. The recall affects 519 cartons distributed nationwide (Lot 1H005, expiration November 30, 2023).

    Product
    DRAXIMAGE MAA — DRAXIMAGE MAA (KIT FOR THE PREPARATION OF TECHNETIUM TC 99M ALBUMIN AGGREGATED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1209-2022·2022-07-20

    Hydroxocobalamin Injection Recalled for Lack of Sterility Assurance

    TMC Acquisition LLC is recalling specific batches of Hydroxocobalamin Preservative Free injectable due to lack of sterility assurance. The affected vials were distributed nationwide in the USA and Puerto Rico.

    Product
    Hydroxocobalamin Preservative Free 5mg/mL, 1mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1198-2022·2022-07-20

    Calcium Chloride Injectable Solution Recalled Due to Sterility Assurance Concerns

    TMC Acquisition LLC is recalling Calcium Chloride Preservative Free injectable solution in 5 mL and 30 mL vials due to lack of assurance of sterility. The recall affects 138 vials distributed nationwide.

    Product
    Calcium Chloride Preservative Free, 100mg/mL, a) 5 mL-vial, b) 30 ml-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V513000·2022-07-20

    2022 BMW X3 Fuel Rail Defect May Cause Engine Fire

    BMW is recalling 2022 X3 xDrive30i vehicles because the high-pressure fuel rail may crack and cause a fuel leak in the engine compartment, increasing the risk of fire. Dealers will replace the fuel rail free of charge.

    Product
    BMW — BMW 228I, X1, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1242-2022·2022-07-20

    Vitamin D3 50,000IU Compounded Product Recalled for Sterility Assurance Failure

    Tailor Made Compounding has recalled Vitamin D3 50,000IU/mL vials nationwide due to lack of sterility assurance during manufacturing. No illnesses have been reported.

    Product
    Vitamin D3 50,000IU/mL, 10mL-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1191-2022·2022-07-20

    CVS Hydrogen Peroxide Bottles Contain Isopropyl Alcohol Due to Label Mix-Up

    CVS Hydrogen Peroxide Topical Solution bottles contain 70% isopropyl alcohol instead of the labeled hydrogen peroxide. The labeling error could lead to misuse and potential harm if consumers use the product as labeled.

    Product
    HYDROGEN PEROXIDE — HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1199-2022·2022-07-20

    Dexpanthenol injectable vials recalled for lack of sterility assurance

    Tailor Made Compounding is recalling 19 vials of Dexpanthenol 250mg/mL due to lack of assurance of sterility. Two batches with different expiration dates were distributed nationwide in the USA and Puerto Rico.

    Product
    Dexpanthenol 250mg/mL, 30mL-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1226-2022·2022-07-20

    Sermorelin Recalled Due to Lack of Sterility Assurance

    Tailor Made Compounding is recalling 1,208 vials of Sermorelin due to inability to assure sterility. The product was distributed nationwide in the USA and Puerto Rico across multiple batch lots.

    Product
    Sermorelin 2000mcg/mL, 7.5mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1240-2022·2022-07-20

    Vitamin B-Complex Injectable Vials Recalled for Lack of Sterility

    Tailor Made Compounding is recalling Vitamin B-Complex injectable vials (10 mL and 30 mL) distributed nationwide USA and Puerto Rico due to lack of assurance of sterility.

    Product
    Vitamin B-Complex, a) 10 mL-vial, b) 30 mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1241-2022·2022-07-20

    Vitamin B-Complex Injectable Vials Recalled for Lack of Sterility Assurance

    Tailor Made Compounding is recalling Vitamin B-Complex Preservative Free injectable vials (batch 03112233B) nationwide due to lack of assurance of sterility. The product should not be used.

    Product
    Vitamin B-Complex Preservative Free, 3ml-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1225-2022·2022-07-20

    Compounded Semaglutide/Cyanocobalamin Vials Recalled Over Sterility Concerns

    Tailor Made Compounding recalled 9,993 vials of compounded semaglutide/cyanocobalamin due to lack of assurance of sterility. No illnesses have been reported.

    Product
    Semaglutide/Cyanocobalamin 5mg/0.2mg/ml, 2ml-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1362-2022·2022-07-20

    Pressure Monitoring Sets with Excess Coating Pose Embolism Risk

    Cook Incorporated is recalling approximately 11,451 Pressure Monitoring Sets because excess coating material on the needle component may enter the bloodstream, potentially causing pulmonary embolism or ischemia.

    Product
    Pressure Monitoring Set, Single-lumen uncoated central venous catheter. RPN C-PMS-250, GPN G02838
    Category
    Medical Device
    Distribution
    Distributed nationwide