The Recall Desk

State

Northern Mariana Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41901–41925 of 73829

  • HighNHTSA·17V481000·2017-07-28

    BMW Recalls Motorcycles with Blocked Rear Reflex Reflectors

    BMW is recalling specific motorcycles because optional aluminum luggage cases may block rear reflex reflectors, increasing crash risk.

    Product
    BMW — BMW F800 GS, F650 GS, F800 GS ADVENTURE, F800 R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V476000·2017-07-27

    Nissan Recalls Infiniti Q50 and Q60 for Fuel Pump Software Defect

    Nissan is recalling 2016-2018 Infiniti Q50 and 2017 Q60 vehicles with 2.0L engines because faulty fuel pump software may cause the engine to stall while driving.

    Product
    INFINITI — INFINITI Q50, Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V477000·2017-07-27

    REV Recalls 2017-2018 Motorhomes With Non-Tempered Headlight Lenses

    REV Recreation Group is recalling 219 motorhomes because headlights may lack tempered glass lenses, which could crack and reduce visibility.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD, MONACO VACATIONER XE, ADMIRAL XE, STORM, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2740-2017·2017-07-26

    Flowonix Recalls Prometra II Pump After Reported Fatal Overdose During MRI

    Flowonix Medical is recalling Prometra II implantable infusion pumps after a report of a fatal drug overdose during an MRI procedure.

    Product
    PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. Manufactured by: Flowonix Medical Inc., --- The correction involves the labeling of the device plus the following Prometra II pump labeling is also being…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2702-2017·2017-07-26

    Penumbra 3D Revascularization Device Recalled Due to Delivery Wire Breakage Risk

    Penumbra Inc. is recalling 155 units of the 3D Revascularization Device because a raw material issue could cause the delivery wire to break, potentially leading to serious injury or death.

    Product
    Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral-M1 and M2 segments) within 8 hours of symptom…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2819-2017·2017-07-26

    Aldi Millville Granola Recalled for Listeria Contamination Risk

    New England Natural Bakers is recalling Aldi Millville Fruit & Nut Whole Grain Granola due to potential Listeria monocytogenes contamination.

    Product
    Millville Fruit & Nut Whole Grain Granola - 16 oz .carton Distributed by Aldi Inc. Batavia, IL 60510 UPC:041498205232
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2817-2017·2017-07-26

    Evoke Organic Muesli Recalled Due to Listeria Contamination Risk

    New England Natural Bakers is recalling Evoke Organic Muesli Classic Swiss 12 oz. pouches due to potential Listeria monocytogenes contamination.

    Product
    Evoke Organic Muesli Classic Swiss 12 oz. pouch UPC: 853305003081
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0991-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection, 7 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5284 NDC# 61553-284-48
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0990-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection, 40 mMol in 250 mL in 250 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5301 NDC# 61553-301-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V474000·2017-07-26

    Mazda Recalls Vehicles for Air Bag Inflator Rupture Risk

    Mazda is recalling specific 2003-2008 models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA MAZDA6, RX-8, MAZDASPEED6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2751-2017·2017-07-26

    BD 3ml Syringes Recalled for Insufficient Sterilization Irradiation

    Becton Dickinson is recalling 648,000 units of BD 3ml Syringes because several lots did not receive the specified dose of irradiation required to meet the Sterility Assurance Level.

    Product
    BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0995-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 5% Dextrose Injection, 9 mMol in 50 mL in 50 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5310 NDC# 61553-310-41
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0997-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection because a media fill failure at the manufacturer raised concerns about sterility.

    Product
    Potassium PHOSphate in 5% Dextrose Injection, 15 mMol in 250 mL in 250 mL Intravia Bag Service, Rx Only. PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5300 NDC# 61553-300-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0986-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection, 10 mMol in a) 100 mL in 150 mL Intravia Bag (NDC 61553-288-48) Service Code: 2K5288, and b) 250 mL in 250 mL Intravia Bag (NDC 61553-281-11) Service Code: 2K5281, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2752-2017·2017-07-26

    BD 10mL Syringes Recalled for Insufficient Sterilization Irradiation

    Becton Dickinson is recalling 547,600 units of BD 10mL Syringes because several lots did not receive the specified dose of irradiation required to meet Sterility Assurance Level standards.

    Product
    BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0989-2017·2017-07-26

    PharMedium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMedium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 5% Dextrose Injection, 30 mMol 500 mL in 500 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5283 NDC# 61553-283-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0994-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection, 9 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5286 NDC# 61553-286-48
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0992-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection because of a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection, 7.5 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5298 NDC# 61553-298-48NDC# 61553-298-48
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0996-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure at the manufacturer that raises concerns about sterility.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection, 30 mMol in a) 250 mL in 250 mL Intravia Bag Service Code 2K5290 NDC# 61553-290-11, b) 500 mL in 500 mL Intravia Bag Service Code 2K5285 NDC# 61553-285-03, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2818-2017·2017-07-26

    Evoke Organic Muesli Recalled Due to Listeria Contamination Risk

    New England Natural Bakers is recalling Evoke Organic Muesli Athlete Fuel pouches due to potential Listeria monocytogenes contamination.

    Product
    Evoke Organic Muesli Athlete Fuel -12 oz .pouch UPC: 853305003029
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0985-2017·2017-07-26

    PharMedium Recalls Succinylcholine Chloride Injection Due to Sterility Concerns

    PharMedium Services is recalling specific lots of Succinylcholine Chloride Injection due to a media fill failure that compromised sterility assurance.

    Product
    Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV Use, PharMedium Services, LLC, Cleveland, MS --- NDC 61553-364-65
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0988-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that raises concerns about sterility.

    Product
    Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5287 NDC# 61553-287-48
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2816-2017·2017-07-26

    New England Natural Bakers Organic Muesli Recalled for Listeria Risk

    New England Natural Bakers is recalling Organic Muesli due to potential Listeria monocytogenes contamination. Consumers should check their pantry for the affected product.

    Product
    New England Natural Bakers Organic Muesli -5lb and 25 lb. cases UPC: 00046689225013
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0993-2017·2017-07-26

    PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns

    PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.

    Product
    Potassium PHOSphate in 5% Dextrose Injection, 7.5 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5299 NDC# 61553-299-48
    Category
    Drug
    Distribution
    Distributed nationwide