The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45151–45175 of 73832

  • SevereFDA (Drugs)·D-0178-2017·2016-12-14

    North American Rescue Recalls Advance Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Advance Trauma Kits because the manufacturer has concerns regarding the sterility of the eye wash irrigating solution.

    Product
    Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0702-2017·2016-12-14

    Thayer MANOS EX Surgical Device Recalled for Missing Safety Warning

    Thayer Intellectual Property, Inc. is recalling 339 MANOS EX surgical devices because customers were not notified of a critical safety warning regarding device bending and breakage.

    Product
    MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal ligament in patients with Carpal Tunnel Syndrome who fail conservative therapy. Plantar Fasciotomy: as a tool for tissue recession in patients with plantar…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0672-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez Global LLC is recalling Oreo Fudge Creme cookies (Original and Mint varieties) because milk is not declared on the ingredient list.

    Product
    Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026967
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0701-2017·2016-12-14

    3M Recalls Universal Electrosurgical Pads Due to Unintended Material Defect

    3M is recalling Universal Electrosurgical Pads because an unintended process liner may impede the safe return of electrosurgical current, increasing the risk of patient burns.

    Product
    3M Universal Electrosurgical Pad, REF 9130 (100 pads / case) and 3M Universal Electrosurgical Pad with Cord, REF 9135-LP (40 pads / case) Product Usage: 3M Universal Electrosurgical Pads are designed to work with most electrosurgical unite (ESU) for virtually every…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0179-2017·2016-12-14

    North American Rescue Recalls K-9 Trauma Field Kits Due to Sterility Concerns

    North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.

    Product
    K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V900000·2016-12-14

    Mercedes-Benz Recalls Vehicles for Potential Axle Bolt Fracture Risk

    Mercedes-Benz is recalling certain 2015-2016 models because axle bolts may not have been assembled correctly, potentially fracturing and causing vehicle instability.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML250, AMG GL63, GL550, ML400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0180-2017·2016-12-14

    North American Rescue Recalls Amphibious Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling Amphibious Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.

    Product
    Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0175-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.

    Product
    Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0609-2017·2016-12-14

    Calbee Recalls Black Pepper Green Pea Crisps Due to Undeclared Milk

    Calbee North America is recalling one lot of black pepper flavored green pea crisps because they may contain undeclared milk.

    Product
    HARVEST SNAPS, SNAPEA CRISPS, BLACK PEPPER FLAVORED GREEN PEA CRISPS, NET WT 3.3 OZ (93g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V899000·2016-12-14

    Mercedes-Benz Recalls Vehicles Due to Electric Power Steering Defect

    Mercedes-Benz is recalling specific 2013-2016 models because a steering control unit defect may cause loss of power steering assist or a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E350, S550, SL550, S600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0183-2017·2016-12-14

    North American Rescue Recalls USCG Boat Response Kits Due to Sterility Concerns

    North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    USCG Boat Response Kit - Product Code 80-0353, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0671-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez is recalling Oreo Fudge Creme cookies because milk is not listed on the ingredient label.

    Product
    Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026943
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0182-2017·2016-12-14

    North American Rescue Recalls Aid Backpack Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    Aid Backpack Kit - Product Code 85-0917, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V897000·2016-12-14

    Triple E Recalls 2017 Serenity S24CB RVs Due to Wiring Fire Risk

    Triple E is recalling 18 model year 2017 Serenity S24CB recreational vehicles because an incorrectly connected circuit wire poses a fire risk.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V898000·2016-12-14

    KZRV Recalls 2016-2017 Durango and Venom Trailers for Door Hinge Defect

    KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.

    Product
    KZRV — KZRV DURANGO, VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0176-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.

    Product
    Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0674-2017·2016-12-14

    Plush Puffs Marshmallows Recalled for Undeclared Milk Allergen

    To Your Heart's Content is recalling Plush Puffs Marshmallows in Toasty Coconut flavor because the product contains undeclared milk.

    Product
    Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16E093000·2016-12-14

    MORryde Recalls Zero G Ramp Door Hinges Due to Insufficient Welds

    MORryde is recalling approximately 2,500 Zero G Ramp Door hinges manufactured between August 21, 2016, and December 12, 2016, because insufficient welds may cause the door to swing down with excessive force.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0707-2017·2016-12-14

    Merge Healthcare Recalls eFilm Workstation Software Due to Measurement Errors

    Merge Healthcare is recalling eFilm Workstation software versions 2.1 through 4.1 because RF projection images may display incorrect measurements without a calibration indicator.

    Product
    Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a software application that is used for viewing medical images. eFilm Workstation with Modules receives digital images and data from various sources (including but not limited to CT, MR, US, RF units…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0721-2017·2016-12-14

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation software versions 4.0, 4.5, 4.7, and 5.0 due to potential inaccuracies in proton dose calculations for specific treatment plans.

    Product
    RayStation 4.0, 4.5, 4.7 and 5.0; Radiation Therapy Treatment Planning System Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V896000·2016-12-14

    DRV Recalls 2017 Full House Trailers Due to Door Hinge Weld Defect

    DRV Suites is recalling 2017 Full House recreational trailers because rear cargo door hinge welds may be insufficient, causing the door to swing down with excessive force.

    Product
    DRV — DRV FULL HOUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0623-2017·2016-12-14

    Green Dirt Farm Sheep's Milk Cheese Recalled for Staphylococcus Aureus Contamination

    Green Dirt Farm is recalling "Dirt Lover" sheep's milk cheese due to Staphylococcus aureus contamination exceeding action limits.

    Product
    Green Dirt Farm "Dirt Lover" sheep's milk cheese packaged in cases of 8, 4-6 oz.. units, sold by case weight. Made by Green Dirt Farm, LLC, Weston, MO 64098.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0622-2017·2016-12-14

    Green Dirt Farm Ruby Blended Milk Cheese Recalled for Staphylococcus Aureus

    Green Dirt Farm is recalling Ruby blended milk cheese due to Staphylococcus aureus contamination exceeding action limits.

    Product
    Green Dirt Farm "Ruby" blended milk cheese packaged in cases of 6, 10 - 12 oz.. units, sold by case weight. Made by Green Dirt Farm, LLC, Weston, MO 64098.
    Category
    Food
    Distribution
    Distributed nationwide