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.

56926–56950 of 73850

  • HighFDA (Devices)·Z-2292-2014·2014-09-17

    Siemens Medical Imaging Systems Recalled for Potential Radiation Overexposure

    Siemens is recalling 192 Luminos dRF, Ysio, and Uroskop Omnia systems because a software malfunction may cause longer radiation exposure than required.

    Product
    Siemens Luminos dRF, Ysio or Uroskop Omnia systems. The Axiom Luminos dRF is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2615-2014·2014-09-17

    Baxter Recalls Buretrol Solution Sets Due to Chamber Separation

    Baxter Healthcare is voluntarily recalling specific lots of Buretrol Solution Sets because the burette chamber may separate from the drip chamber.

    Product
    ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m), 150 mL Burette***Drip Chamber Filter Valve 3 Luer Activated Valves***Male Luer Lock Adapter***with Retractable Collar***Fluid path is Sterile, Nonpyrogenic.***Indications for Use: For the administration of fluids from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2613-2014·2014-09-17

    Baxter Recalls Buretrol Solution Sets Due to Chamber Separation

    Baxter Healthcare is voluntarily recalling specific lots of Buretrol Solution Sets because the burette chamber may separate from the drip chamber.

    Product
    ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 Injection Sites Male Luer Lock Adapter with***Retractable Collar***Fluid path is Sterile, Nonpyrogenic***Indications for Use: For the administration of fluids from a container into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2602-2014·2014-09-17

    Wright Medical Recalls CLAW II Orthopedic Plates Due to Material Error

    Wright Medical Technology is recalling 1,127 CLAW II 2 Hole Plate Ortholoc 3DSi units because they were manufactured from an incorrect raw material.

    Product
    CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 20mm, REF 40240220, 1 EACH, Rx ONLY, NON STERILE Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1569-2014·2014-09-17

    Chirothin Dietary Supplement Recalled for Unapproved Human Chorionic Gonadotropin

    ChiroNutraceutical LLC is recalling Chirothin dietary supplement bottles because the product contains unapproved human chorionic gonadotropin (hCG) and was marketed without an approved NDA or ANDA.

    Product
    CHIROTHIN Dietary Supplement, 2 Fl Oz (60 ml), OTC. Manufactured for ChiroNeutraceutical, 877-377-7636, Chesterfield, MO 63005.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·14276·2014-09-16

    IKEA Recalls GUNGGUNG Children's Swing Due to Fall Hazard

    IKEA is recalling GUNGGUNG children's swings because suspension fittings can break, causing children to fall. Consumers should remove the swing and return it for a refund.

    Product
    GUNGGUNG child's swing
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V565000·2014-09-15

    Nissan Recalls 2013 Altima Vehicles for Hood Latch Interference

    Nissan is recalling 2013 Altima vehicles because hood latch interference may cause the hood to open while driving, increasing crash risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·058-2014·2014-09-12

    Claude's Beef Jerky Recalled for Undeclared Allergens and Lack of Inspection

    Jerky By Art is recalling Claude's Beef Jerky with Red Chile because it was produced without USDA inspection and contains undeclared wheat and anchovies.

    Product
    New Mexico Firm Recalls Beef Jerky Products Produced Without the Benefit of Inspection and Misbranded With Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V562000·2014-09-12

    Mitsubishi Recalls Lancer and Outlander Vehicles for Engine Belt Defect

    Mitsubishi is recalling 2008-2011 Lancer, Lancer Evolution, and Outlander models because the engine drive belt may detach, causing the engine to stall and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI LANCER SPORTBACK RALLIART, LANCER RALLIART, LANCER RALIART, LANCER SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V560000·2014-09-12

    Mitsubishi Recalls 2011 Outlander Sport for Brake Booster Defect

    Mitsubishi is recalling certain 2011 Outlander Sport vehicles because a cracked brake booster switch sleeve may prevent the brake pedal from returning, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V558000·2014-09-12

    Halcore Recalls 2014 Horton Ambulances with Liquid Spring Suspension Kits

    Halcore is recalling 29 model year 2014 Horton ambulances equipped with Liquid Spring aftermarket suspension kits because the fluid tank mounting bracket may fail.

    Product
    HORTON AMBULANCE — HORTON AMBULANCE 623, 457, 403, 603
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V561000·2014-09-12

    Jayco Recalls 2015 Jay Flight Trailers Due to Ladder Mounting Defect

    Jayco is recalling 2015 Jay Flight 19RD trailers because the roof ladder may be installed on the wrong side without proper support, increasing injury risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V555000·2014-09-11

    Volvo Recalls 2014-2015 Trucks Due to Brake Caliper Bolt Torque Issue

    Volvo is recalling 3,175 model year 2014-2015 VAH, VNL, and VNM trucks because disc brake caliper bolts may not be tightened to specification, increasing crash risk.

    Product
    VOLVO — VOLVO VNM, VAH, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V554000·2014-09-11

    Mack Trucks Recalls 2015 Granite Trucks Due to Fuel Filter Defect

    Mack Trucks is recalling 2015 Granite trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    MACK — MACK GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14753·2014-09-11

    Arctic Cat Recalls Wildcat Trail Side-by-Sides Due to Fire Hazard

    Arctic Cat is recalling about 5,600 Wildcat Trail and Wildcat Trail XT side-by-side utility vehicles because oil can leak from the oil cooler lines, posing a fire hazard.

    Product
    Arctic Cat Wildcat Trail and Wildcat Trail XT Side by Side
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14275·2014-09-11

    Kidde Recalls Hard-Wired Smoke and Combination Smoke/CO Alarms Due to Failure

    Kidde is recalling about 1.3 million hard-wired smoke and combination smoke/CO alarms because they may fail to alert users during a power outage. No injuries have been reported.

    Product
    Kidde hard-wired smoke and combination smoke/carbon monoxide (CO) alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V556000·2014-09-11

    Toyota Recalls 2014 Tundra CrewMax and Double Cab for Air Bag Defect

    Toyota is recalling 2014 Tundra CrewMax and Double Cab vehicles because a B-pillar trim misinstallation may prevent side air bags from deploying properly in a crash.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V553000·2014-09-11

    Mack Trucks Recalls 2015 Models Due to Seat Belt Bolt Torque Defect

    Mack Trucks is recalling 2015 CHU, CXU, and GU trucks because seat belt bolts may not be torqued correctly, risking detachment in a crash.

    Product
    MACK — MACK GRANITE (GU), CHU, PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V557000·2014-09-11

    Volvo Recalls 2015 VNL and VNX Trucks for Engine Stall Risk

    Volvo is recalling 2015 VNL and VNX trucks because a software error may cause the engine to stall while driving, increasing crash risk.

    Product
    VOLVO — VOLVO VNL, VNX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2486-2014·2014-09-10

    Customed Recalls Surgical Packs Due to Potential Packaging Integrity Issues

    Customed, Inc. is recalling specific lots of EO-sterilized surgical packs because packaging integrity may be compromised, potentially leading to product contamination or loss of sterility.

    Product
    Shoulder pack (I) (2), code 900-2515 (1) GOWN IMP. XTRA REINF. XL TOWEL WRAP LEVEL Ill (1) TOWEL ABSORBENT 15" X 20" (1) GOWN XXL SMS IMPERVIOUS REINFORCED (1) MAYO STAND COVER REINFORCED (2) STRIPS TAPE 24" X 4" (1) SUTURE BAG FLORAL (1) SHEET SPLIT W/ADHESIVE 1 08" X…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2321-2014·2014-09-10

    Customed Recalls Major Lap Packs Due to Potential Packaging Integrity Issues

    Customed, Inc. is recalling Major Lap Packs because packaging integrity may be compromised, potentially leading to product contamination or loss of sterility.

    Product
    MAJOR LAP PACK - (1) TABLE COVER REINF. 50" X 90" 10) GUZE SPONGE 4" X 4" 16PLY XRD (1) DRAPE T LAPAROT 102" X 78" X 121" SMS (1) UTILITY BOWL 32oz (1) TUBE CONNECT. SUCTION W X 12' (1) CAUTERY TIP POLISHER (1) YANKAUER SUCTION TUBE W/0 VENT (4) DRAPE UTILITY WITH TAPE (2)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2453-2014·2014-09-10

    Customed Recalls Vaginal Procedure Packs Due to Packaging Integrity Concerns

    Customed, Inc. is recalling vaginal procedure packs because packaging integrity may be compromised, potentially leading to product contamination or loss of sterility.

    Product
    VAGINAL PROCEDURE PACK CUSTOM ED CONTENTS: (1) DRAPE LITHOTOMY 110" X 63" W/LEGGINGS I POUCH FEN 3 X 6 SMS LIF (1) GOWN XL SMS IMPERV. REINFORCED LIF (1) COVER MAYO STAND REINFORCED LIF (1) BAG SUTURE FLORAL (1) COVER TABLE REINF 50" X 90" LIF (1) TUBE…
    Category
    Medical Device
    Distribution
    Distributed nationwide