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.

44576–44600 of 73832

  • ModerateFDA (Devices)·Z-1039-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Update

    Endologix is updating the Instructions for Use and implementing modifications to the AFX Endovascular AAA System.

    Product
    AFX Endovascular AAA System, Endoleak Type: IIIB Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment The AFX Endovascular AAA System is intended for endovascular treatment of patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1049-2017·2017-01-25

    Endologix AFX2 Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling the AFX2 Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-40 F00820-02 BEA28-100/I20-40 F00820-03 BEA28-80/I20-40 F00820-06 BEA28-120/I16-40 F00820-07 BEA28-100/I16-40 F00820-08 BEA28-80/I16-40 F00820-09 BEA28-60/I16-40 F00820-16…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0434-2017·2017-01-25

    Perrigo Recalls Clindamycin and Benzoyl Peroxide Gel Due to Mold

    L. Perrigo Company is recalling 162,534 tubes of Clindamycin Phosphate and Benzoyl Peroxide Gel because a small number of tubes may contain mold on the cap.

    Product
    CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE — CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE (CLINDAMYCIN, BENZOYL PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1024-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Liners Due to Labeling Mismatch

    Zimmer Biomet is recalling 36 units of ArComXL polyethylene liners because packaging labels did not match the physical product, posing a risk of surgical delay.

    Product
    RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1037-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Updated

    Endologix updated the Instructions for Use and modified the AFX Endovascular AAA System. The correction applies to procedures conducted after July 2015.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment The AFX Endovascular AAA System is intended for endovascular treatment of patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1048-2017·2017-01-25

    Endologix AFX Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling 34 units of the AFX Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75 V F0070308 A2828/C75 V F0070312 A3434/C80 V f00553 I1616/C55F SA F00556 I2013/C70F SA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1041-2017·2017-01-25

    Smith & Nephew RENASYS GO Wound Therapy Recall for Clearance Issue

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy devices because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2017·2017-01-25

    Smith & Nephew RENASYS GO Power Supply Recalled for Regulatory Clearance

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy External Power Supply Units because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0433-2017·2017-01-25

    Novum Pharma Recalls Subpotent Novacort Gel Sample Packets

    Novum Pharma is recalling Novacort Gel sample packets because the pramoxine hydrochloride content was found to be out of specification.

    Product
    Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0431-2017·2017-01-25

    Teva Recalls Risedronate Sodium Tablets for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.

    Product
    Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V052000·2017-01-24

    Ford Recalls 2016 Focus and C-Max for Floor Pan Welding Defect

    Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.

    Product
    FORD — FORD FOCUS, C-MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17071·2017-01-24

    HP Recalls Lithium-Ion Notebook Batteries Due to Fire and Burn Hazards

    HP is expanding a recall of about 101,000 lithium-ion batteries for HP and Compaq notebook computers because they can overheat, posing fire and burn risks.

    Product
    Lithium-ion batteries used in HP notebook computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V051000·2017-01-24

    Toyota Recalls 2016-2017 Tundra Trucks for Rear Bumper Defect

    Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V053000·2017-01-24

    Ford Recalls 2017 F-150 Trucks Due to Instrument Cluster Power Loss

    Ford is recalling 2017 F-150 trucks because the instrument cluster may lose power in cold weather, potentially hiding the transmission gear position and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V050000·2017-01-23

    Autocar Recalls 2013-2016 Xpeditor Trucks Due to Brake Defect

    Autocar is recalling 38 Xpeditor trucks from 2013-2016 because over-braking can cause S-cam tube bolts to loosen, leading to unexpected brake engagement and increased crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E005000·2017-01-23

    IH Parts Recalls Steering Tie Rod Adjusters for Fracture Risk

    IH Parts America Inc. is recalling specific steering tie rod adjusters for International Scout vehicles because they may fracture, affecting steering capability and increasing crash risk.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V047000·2017-01-20

    BMW Recalls 2000-2003 Models for Driver Air Bag Inflator Rupture Risk

    BMW is recalling specific 2000-2003 3, 5, and X5 series vehicles because replacement driver-side air bag inflators may rupture during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW 323, 320, 325, 330
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V048000·2017-01-20

    Walker Recalls 2014-2017 Food Grade Tank Trailers for Underride Guard Defect

    Walker is recalling 2014-2017 Food Grade Tank Trailers because weld joints on the underride guard may crack, potentially causing the guard to detach and become a road hazard.

    Product
    WALKER — WALKER FOOD GRADE TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V046000·2017-01-20

    Maserati Recalls 2014-2017 Models for Seat Wiring Fire Risk

    Maserati is recalling 39,381 vehicles due to a front seat wiring harness defect that may cause an electrical short and increase the risk of a fire.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE, LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2017·2017-01-20

    Hans Kissle Recalls Ready-To-Eat Chicken Bowls Due to Processing Defect

    Hans Kissle Company is recalling approximately 6,348 pounds of ready-to-eat chicken bowls due to a potential process defect that could allow bacterial pathogens to survive.

    Product
    Hans Kissle Company, LLC — Hans Kissle Company, LLC. Recalls Ready-To-Eat Chicken Products Due To Potential Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17E004000·2017-01-20

    New Haven Recalls Wheelchair Securement Tiedowns Due to Crash Risk

    The New Haven Companies is recalling Safe Haven Wheelchair Securement Tiedowns because they may not adequately secure a wheelchair in a crash, increasing injury risk.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V044000·2017-01-20

    Airstream Recalls 2017 Trailers Due to Incorrect Tire Certification Labels

    Airstream is recalling 2017 Sport, International, and Flying Cloud trailers because incorrect tire labels could lead to overinflation and tire blowouts.

    Product
    AIRSTREAM — AIRSTREAM INTERNATIONAL, SPORT, FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide