The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59901–59925 of 73856

  • SevereFDA (Food)·F-0782-2014·2013-12-25

    National Enzyme Recalls Digestive Bul Powder for Chloramphenicol Contamination

    National Enzyme Co is recalling Bulk A957 Nutra Med Digestive Bul powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A957 Nutra Med Digestive Bul powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83318);
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1130-2014·2013-12-25

    Senor Murphy Candymaker Recalls Multiple Candies Due to Undeclared Allergens

    Senor Murphy Candymaker is recalling eight types of candy products because they contain undeclared allergens.

    Product
    Senor Murphy Santa Fe Candymaker Chili Peanut Brittle , 4 oz and 1 lb. Handmade with sugar, corn syrup, peanuts, butter, soda, chile, and salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0539-2014·2013-12-25

    Baxter ABACUS TPN Calculation Software Recalled for Data Corruption Risk

    Baxter is voluntarily correcting ABACUS TPN software versions 2.0-3.0 because data corruption could cause patients to receive another patient's TPN order.

    Product
    ABACUS TPN Calculation Software, Baxa: 8300-0045 ABACUS CE (Calculator Edition), 8300-0046 ABACUS SE (Single-Workstation Edition), 8300-0047 ABACUS ME (Multi-Workstation Edition) ABACUS is a Windows¿ - based order entry TPN software application for comprehensive calculations…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0538-2014·2013-12-25

    Remel Inc. Recalls Streptex Latex D Reagent for False Negative Results

    Remel Inc. is recalling 109 kits of Streptex Latex D reagent because the product may produce weak or false negative test results for streptococcal group D.

    Product
    Streptex* Latex D, Ref R30950901 ZL54, IVD, Latex reagent for streptococcal group D, 50 tests per box. The firm name on the label is Remel Inc., Lenexa, KS, Manufactured by Remel Europe Ltd., Dartford Kent, UK. Streptex is a rapid latex test system for use in the qualitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0524-2014·2013-12-25

    GE Recalls InstaTrak and ENTrak Computer-Assisted Navigation Systems

    GE OEC Medical Systems is recalling InstaTrak and ENTrak navigation systems due to potential safety issues.

    Product
    InstaTrak¿ 3500 Plus, ENTrakTM Plus, InstaTrak¿ 3500, ENTrakTM Computer-Assisted Navigation Systems (USA),
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2014·2013-12-25

    Intuitive Surgical Recalls Mega Needle Drivers for Potential Jaw Detachment

    Intuitive Surgical is recalling Mega Needle Drivers for the da Vinci S and Si systems due to a potential risk of jaw insert detachment.

    Product
    Mega Needle Driver, 8MM assembly of the da Vinci S IS1200 and da Vinci Si, IS2000. Manufactured by Intuitive Surgical, Sunnyvale, CA. EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1126-2014·2013-12-25

    Senor Murphy Candymaker Recalls Chocolate Pretzels for Undeclared Allergens

    Senor Murphy Candymaker is recalling Chocolate Pretzels and other confections due to undeclared allergens. Consumers should stop using the products.

    Product
    Senor Murphy Santa Fe Candymaker Chocolate Pretzels 3 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0545-2014·2013-12-25

    ASI Medical Recalls SEAC Advanced Dental Systems Due to Air Tank Rupture Risk

    ASI Medical is recalling 337 SEAC Advanced Dental Systems because the miniature plastic air tank can potentially rupture.

    Product
    SEAC Advanced Dental System, Model A591561 The SEAC Advanced Dental System is a self-contained dental delivery system with a built-in air compressor,vacuum system and water supply. It is designed operate dental handpiece attachments and suction instruments. The SEAC Advanced…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1124-2014·2013-12-25

    Senor Murphy Candymaker Recalls Multiple Candies for Undeclared Allergens

    Senor Murphy Candymaker is recalling eight candy products due to undeclared allergens. Consumers should stop eating these items and check the recall list.

    Product
    Senor Murphy Santa Fe Candymaker Cashew Crunch , 4oz and 1 lb. Handmade with cashews, sugar, corn syrup, butter, soda, and salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0522-2014·2013-12-25

    Mobility Unlimited Recalls KayserBetten IDA Beds Due to Door Joint Failure

    Mobility Unlimited Inc. is recalling 33 KayserBetten model IDA beds because door joints may loosen or separate, causing doors to drop outward and potentially injure users.

    Product
    KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0517-2014·2013-12-25

    Siemens Recalls Dimension TACR Flex Reagent Cartridges for Stability Issues

    Siemens is recalling Dimension TACR Flex reagent cartridges because reduced stability may cause inaccurate test results for transplant patients.

    Product
    Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is an in vitro diagnostic test intended to quantitatively measure Tacrolimus in human whole blood on the Dimension(R) clinical chemistry system. Measurements of Tacrolimus are used as an aid in the management…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1128-2014·2013-12-25

    Senor Murphy Candymaker Recalls Multiple Confections for Undeclared Allergens

    Senor Murphy Candymaker is recalling eight confection products due to undeclared allergens. Consumers should stop eating these items and return them to the point of purchase.

    Product
    Senor Murphy Santa Fe Candymaker Pinon Brittle , 4 oz and 1 lb. Handmade with pinones (pine nuts), sugar, corn syrup, butter, soda, and salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0521-2014·2013-12-25

    Intuitive Surgical Recalls Large Needle Drivers Due to Jaw Insert Detachment Risk

    Intuitive Surgical is recalling Large Needle Drivers for the da Vinci S and Si systems because the jaw insert may detach during use.

    Product
    Large Needle Driver, 8MM assembly of the da Vinci S IS1200 and da Vinci Si, IS2000. Manufactured by Intuitive Surgical, Sunnyvale, CA. EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0537-2014·2013-12-25

    Remel Inc Recalls Streptex Kits Due to Potential False Negative Results

    Remel Inc is recalling 768 Streptex kits because they may produce weak or false negative test results for Streptococcal grouping.

    Product
    Streptex* kit, Ref R30950501 ZL50, Rapid latex test for Streptococcal grouping, IVD. The kit contains reagent groups A, B, C, D, F, G, a control, and an extraction enzyme. The firm name on the label is Remel Europe Ltd., Dartford, England. Streptex is a rapid latex test…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1127-2014·2013-12-25

    Senor Murphy Candymaker Recalls Multiple Products for Undeclared Allergens

    Senor Murphy Candymaker is recalling eight candy products due to undeclared allergens. The recall covers nationwide distribution.

    Product
    Senor Murphy Santa Fe Candymaker Chile Peanuts, 4 and 9 oz. Handmade with peanuts, sugar, corn syrup, brown sugar, butter, baking soda, Shimayo red chile, and salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1123-2014·2013-12-25

    Senor Murphy Candymaker Recalls Pecan Bueno for Undeclared Allergens

    Senor Murphy Candymaker is recalling Pecan Bueno and other products due to undeclared allergens. Consumers should stop eating these items.

    Product
    Senor Murphy Santa Fe Candymaker Pecan Bueno, 4oz and 1 lb. Handmade with pecans, sugar, corn syrup, butter, soda, and salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2014·2013-12-25

    Kimberly-Clark Epidural Pain Management Trays Recalled for Syringe Defect

    Kimberly-Clark is recalling Single Shot Epidural Pain Management Trays because the included BD LOR Syringes may stall or stick.

    Product
    Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0525-2014·2013-12-25

    Ortho-Clinical Diagnostics Recalls VITROS CA 125 II Calibrators

    Ortho-Clinical Diagnostics is recalling VITROS CA 125 II Calibrators due to a positive shift in patient results.

    Product
    VITROS CA 125 II Calibrators For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, VITROS 3600 Immunodiagnostic System and VITROS 5600 Integrated System for the quantitative measurement of OC 125 defined antigen in human serum and plasma (EDTA or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0533-2014·2013-12-25

    Integra Epidural Anesthesia Kits Recalled Due to Syringe Plunger Defect

    Integra LifeSciences is recalling specific lots of epidural anesthesia kits because the included BD LOR syringe plunger may stall or stick.

    Product
    Integra Disposable, Convenience Kit Single Shot Epidural Tray Reorder Number 340269 Rx Only Product Usage: The Integra kits which contain a BD LOR syringe are intended to provide licensed medical professionals with a kit containing drugs and other medical devices that are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1125-2014·2013-12-25

    Senor Murphy Candymaker Recalls Chocolate Products Due to Undeclared Allergens

    Senor Murphy Candymaker is recalling multiple chocolate and nut products because they contain undeclared allergens.

    Product
    Senor Murphy Santa Fe Candymaker Chile Pistachio Bark , 2.5 oz and 1 lb. Handmade with dark chocolate (sugar, chocolate liquor processed with alkali, cocoa butter, milk fat, soy lecithin - an emulsifier, natural flavors), pistachios, chile, salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1100-2014·2013-12-25

    Source Naturals Essential Enzyme Ultra Recalled for Chloramphenicol Contamination

    Source Naturals Essential Enzyme Ultra is being recalled because it was made with bulk products containing chloramphenicol.

    Product
    Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme Blend; 30, 60, 90 & 120 count bottles. Vegetarian capsules Manufactured for: Source Naturals, Inc. Santa Cruz, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0768-2014·2013-12-25

    National Enzyme Recalls Carbgestkosh Capsules Due to Chloramphenicol Contamination

    National Enzyme Co is recalling bulk Carbgestkosh capsules because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 9809 ENZYMEDICA CARBGESTKOSH capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92103).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0496-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Shelf-Life Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED C 15OCM; Catalog Number: M0031441940; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0546-2014·2013-12-25

    Arrow International Recalls Nerve Block Catheter Kits Due to Labeling Error

    Arrow International is recalling 121 Continuous Peripheral Nerve Block Catheter Kits because the packaging incorrectly describes the stimulator cable connector.

    Product
    Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Block Catheter Kit and Set permits placement of catheters next to nerves and nerve plexuses for continuous nerve block anesthesia or analgesia techniques for periods not exceeding 72 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide