The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56201–56225 of 73850

  • HighFDA (Devices)·Z-0185-2015·2014-11-19

    GE Healthcare Recalls Varicam and VG Hawkeye Nuclear Medicine Devices

    GE Healthcare is recalling 478 nuclear medicine imaging devices because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    GE Healthcare Varicam/VG and VG Hawkeye devices. Models H3000YA, H3000YB, H3000YC, H3000YD, H2508PA, H2508PB, H2508PC, H2508PD. Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0197-2015·2014-11-19

    Integra Titan Reverse Shoulder System Cutting Templates Recalled for Manufacturing Error

    Integra LifeSciences Corp. is recalling 12 units of Reverse Shoulder System cutting templates because the threaded handle was welded backwards, resulting in an incorrect cutting angle.

    Product
    Integra Titan Reverse Shoulder System right and left head cutting templates, 142.5 degrees. The Reverse Shoulder System Cutting Template, 142.5 degrees is an accessory for use with the Integra Titan Reverse Shoulder System. It is used to project the osteotomy angle on the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2015·2014-11-19

    Mondelez Recalls Chiclets Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    Chiclets Gum, 200 - 2 piece packs (400 pieces), Retail UPC 0 12546 02509 6, Case UPC 10012546108499
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0189-2015·2014-11-19

    GE Healthcare Recalls Brivo NM615 Nuclear Imaging Systems Due to Loose Fasteners

    GE Healthcare is recalling 22 Brivo NM615 nuclear imaging systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    Brivo NM615, is an all-purpose, single detector integrated nuclear imaging system. Models H3100TP, H3100TN, H3100TT, H3100TR, H3100TW, H3100WZ, H2401MP, H2401MN, H2401MT, H2401MR, H2401MW, H2401NJ. Product Usage: The Brivo NM 615 is an emission computed tomography system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0500-2015·2014-11-19

    Mondelez Recalls Chiclets Peppermint Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Peppermint Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    1) Chiclets Peppermint Gum, 6-10 piece packages (60 pieces), Retail UPC 0 12546 10105 9; 2)Chiclets Peppermint Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02501 0, Case UPC 1001254 3)Chiclets Peppermint Gum, (12 pieces), Retail UPC 0 12546 10128 8; 4)Chiclets…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0187-2015·2014-11-19

    GE Healthcare Recalls Discovery NM 630 Nuclear Imaging Systems

    GE Healthcare is recalling 147 Discovery NM 630 nuclear imaging systems to update maintenance procedures and prevent loose fasteners from causing parts to fall on patients.

    Product
    Discovery NM 630, dual detector free-geometry integrated nuclear imaging system. Models H3100RC, H3100RD, H2401LW. Product Usage: The GE Discovery NM 630 system is a medical tool intended for use by appropriately trained healthcare professionals to aid in detecting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2015·2014-11-19

    Roscoe Medical Recalls Transport Rollators Due to Caster Separation Risk

    Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.

    Product
    Transport Rollator with Padded Seat; Large 8-inch wheels with wheel locks (indoor and outdoor use), fold down footrests, ergonomic handles, curved padded backrest and handy wire basket for storage. Item# 30192 Burgundy each/Item# 30194 Blue each.. Transport Rollator is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0499-2015·2014-11-19

    Chiclets Gum Recalled for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Assorted Variety Multipak fruit flavor gum due to undeclared soy lecithin on the label.

    Product
    Chiclets Assorted Variety Multipak - Fruit Flavor Gum, 6-10 piece packages (60 pieces), 6 PAK, Retail UPC 0 12546 10102 8; 2)Chiclets Assorted Variety Multipak - Fruit Flavor Gum, 7-6 PAK packages (420 pieces), Retail UPC 0 12546 0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14T016000·2014-11-19

    Bluestar Trailer Tires Recalled for Sidewall Blister Risk

    China Manufacturers Alliance is recalling specific Bluestar trailer tires that may develop sidewall blisters, potentially causing loss of vehicle control.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0245-2015·2014-11-19

    Fougera Recalls Fluocinonide Gel Due to Residual Solvent Concerns

    Fougera Pharmaceuticals is recalling specific lots of Fluocinonide Gel USP, 0.05% because they may not meet USP requirements for residual solvents.

    Product
    FLUOCINONIDE GEL USP, 0.05%, Rx only, For External Use Only, Not For Ophthalmic Use, a) NET WT 15 gram tubes and b) NET WT 60 grams tubes, E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0135-15 (15 g) and NDC 0168-0135-60 (60 g)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0248-2015·2014-11-19

    Assured Naproxen Sodium Tablets Recalled Due to Mispackaging Error

    Contract Packaging Resources Inc. is recalling Assured Naproxen Sodium Tablets because correct labeled bottles of Assured Ibuprofen softgels were mistakenly packaged into Naproxen cartons.

    Product
    Assured Naproxen Sodium Tablets, USP 220 mg., 15 count bottle, Repackaged by Contract Packaging Resources, Inc 8009 Industrial Village Road Greensboro, NC 27409 Distributed by Greenbrier International, Inc Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0211-2015·2014-11-19

    Maquet Cardiohelp-I System Recalled for Potential Software Display Error

    Maquet Cardiovascular is recalling 331 Cardiohelp-I Systems due to a software issue that may display an erroneous 'Battery Needs Service' message after startup.

    Product
    Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide removal system used to pump blood thorough the extracorporeal bypass circuit for circulatory and/or pulmonary support during procedures requiring cardiopulmonary bypass (for periods up to six hours).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0198-2015·2014-11-19

    Zimmer Persona Stemmed 5 Degree Cemented Tibia Recalled for Cleaning Failure

    Zimmer, Inc. is recalling 138 units of Persona Stemmed 5 Degree Cemented Tibia knee components due to a cleaning process validation failure.

    Product
    Persona Stemmed 5 Degree Cemented Tibia Product Usage: This device is indicated for patients with severe knee pain and disability due to:  Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis.  Collagen disorders, and/or avascular necrosis of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0247-2015·2014-11-19

    Fresenius Kabi Recalls Haloperidol Decanoate Injection Due to Impurity Failure

    Fresenius Kabi is recalling Haloperidol Decanoate Injection vials due to an out-of-specification impurity result. The recall covers 216,517 vials distributed nationwide and in Puerto Rico.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·079-2014-EXP·2014-11-18

    City Line Foods Recalls Pretzel Dogs for Undeclared Soy Allergen

    City Line Foods is expanding a recall of 1.2 million pounds of frozen pretzel dog products due to misbranding and undeclared soy lecithin, a known allergen.

    Product
    Pennsylvania Firm Expands Recalls Pretzel Dog Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·15027·2014-11-18

    CoScentrix Recalls DD Brand Candles Due to Fire Hazard

    CoScentrix is recalling approximately 256,000 DD brand candles sold at Hobby Lobby because the high flame can ignite the wax surface, posing a fire hazard.

    Product
    DD Brand Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V737000·2014-11-18

    Mack Trucks Recalls 2015 CHU and CXU Models for Steering Defect

    Mack is recalling 1,048 model year 2015 CHU and CXU trucks because incorrectly positioned tie rod collars may allow ball sockets to come loose, risking loss of steering.

    Product
    MACK — MACK CHU, PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V735000·2014-11-18

    Isuzu Recalls 2012-2014 Reach Chassis Due to Brake Light Switch Defect

    Isuzu is recalling 3,564 model year 2012-2014 Reach chassis because the brake light switch may bend or corrode, potentially failing to activate brake lights and increasing crash risk.

    Product
    ISUZU — ISUZU REACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15028·2014-11-18

    Black Diamond Recalls Whippet Ski Poles Due to Pick Breakage Risk

    Black Diamond Inc. is recalling Whippet and Carbon Whippet ski poles because the stainless steel pick can break, posing a risk of injury to users on slopes.

    Product
    Ski poles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V736000·2014-11-18

    Ford Recalls Fusion Models Due to Key Removal Safety Defect

    Ford is recalling 2014-2015 Fusion, Fusion Hybrid, and Fusion Energi vehicles because the key may be removed while the transmission is not in Park, increasing the risk of rollaway.

    Product
    FORD — FORD FUSION, FUSION HYBRID, FUSION ENERGI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E078000·2014-11-17

    Carefree Latitude Awnings Recalled for Defective Screws on Motorhomes

    Carefree is recalling Latitude Awnings styles GX and G installed on motorhomes due to screws that may not meet specifications, posing a risk of the awning falling.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V734000·2014-11-17

    Fleetwood Bounder Classic Recalled for Loose Grab Bar Risk

    Allied Recreation Group is recalling 2014-2015 Fleetwood Bounder Classic RVs because a grab bar may pull loose, increasing injury risk.

    Product
    FLEETWOOD — FLEETWOOD BOUNDER CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide