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.

55551–55575 of 73850

  • LowFDA (Drugs)·D-0333-2015·2015-01-14

    Akorn Recalls Triamcinolone Acetonide Lotion Due to Impurity Specification Failure

    Akorn, Inc. is recalling 3,937 bottles of Triamcinolone Acetonide Lotion USP, 0.025% because a known impurity exceeded specifications at the 12-month stability point.

    Product
    Triamcinolone Acetonide Lotion USP, 0.025% is supplied in the following size: 60 mL (NDC 61748-219-60).
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·15059·2015-01-13

    IKEA Recalls VYSSA Crib Mattresses Due to Entrapment Hazard

    IKEA is recalling VYSSA crib mattresses because they may create gaps larger than allowed by federal regulations, posing an entrapment risk to infants.

    Product
    VYSSA crib mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2015·2015-01-12

    US Foods Recalls Beef Fajita Strips Due to Undeclared Peanuts

    US Foods is recalling approximately 700 pounds of beef fajita strips because the product contains undeclared peanuts, a known allergen.

    Product
    US Foods Inc — New York Firm Recalls Beef Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V008000·2015-01-12

    Winnebago Recalls 2014-2015 Motorhomes Due to Tire Pressure Monitoring Defect

    Winnebago is recalling 2014-2015 Trend, Travato, and Itasca Viva motorhomes because the tire pressure monitoring system may fail to detect low tire pressure, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, TREND, ITASCA VIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V006000·2015-01-09

    Ford Recalls 2015 Lincoln MKC Vehicles for Ignition Switch Defect

    Ford is recalling 2015 Lincoln MKC vehicles because the push-to-start button may be pressed accidentally, causing the engine to shut off and increasing crash risk.

    Product
    LINCOLN — LINCOLN MKC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V005000·2015-01-09

    Ford Recalls Vehicles Due to Fuel Pump Failure Risk

    Ford is recalling certain 2014-2015 vehicles because a defective fuel pump may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    FORD — FORD, LINCOLN FOCUS, ESCAPE, FIESTA, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15056·2015-01-08

    CoScentrix Expands Recall of DD Brand Candles Due to Fire Hazard

    CoScentrix is expanding its recall of 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
  • SevereCPSC·15058·2015-01-08

    SKLZ Resistance Trainers Recalled Due to Risk of Severe Injury

    Pro Performance Sports is recalling SKLZ Recoil 360 Resistance Trainers because a weld can break, causing the cord to retract and injure users or partners.

    Product
    SKLZ Recoil 360™ All-Position Resistance Trainers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V003000·2015-01-08

    Lance Recalls 2015 Campers and Travel Trailers Due to Awning Bracket Defect

    Lance is recalling 2015 Slide-In Campers and Travel Trailers because awning mounting brackets may crack, causing the awning to fall and potentially injure people.

    Product
    LANCE — LANCE SLIDE-IN CAMPER, TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V004000·2015-01-08

    Thor Motor Coach Recalls 2015 Motorhomes Due to Awning Screw Defect

    Thor Motor Coach is recalling 154 model year 2015 motorhomes because defective awning screws could cause the awning to fall and injure people.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR CHATEAU CITATION, PALAZZO, FOUR WINDS 5000, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0756-2015·2015-01-07

    Safeway Select French Salted Caramel Ice Cream Recalled for Undeclared Peanut

    Safeway Inc is recalling Safeway Select French Salted Caramel Premium Ice Cream because peanut butter was used in the recipe but not listed on the label.

    Product
    Safeway Select French Salted Caramel (Fleur De Sel) Premium Ice Cream; 1.5 quart round paper carton with lid.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0329-2015·2015-01-07

    Ginseng Kianpi Pill Recalled for Undeclared FDA-Approved Drugs

    One and Zen is recalling Ginseng Kianpi Pill capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.

    Product
    GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0889-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment

    Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0896-2015·2015-01-07

    Hansen Medical Recalls Sensei X Robotic Catheter Systems Due to Loose Clamp

    Hansen Medical is recalling Sensei X Robotic Catheter Systems because a mechanical clamp may become loose, causing the device to fall and potentially injure patients or users.

    Product
    Sensei X Robotic Catheter System, model numbers 02057 and 08257. - Set up joint (SUJ)mechanical clamp that secures the SUJ to the catheter laboratory table. Product Usage: The Sensei X Robotic Catheter System is an electromechanical software controlled system designed to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2015·2015-01-07

    Nijiya Market Recalls Frozen Boneless Beef Imported Without Inspection

    Nijiya Market is recalling approximately 359 pounds of frozen boneless beef products produced in Japan that were not presented for USDA inspection at the U.S. point of entry.

    Product
    California Firm Recalls Boneless Beef Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V002000·2015-01-07

    Polaris Recalls Victory Motorcycles Due to Fuel Pump Defect

    Polaris is recalling certain Victory motorcycles because a manufacturing defect may cause the fuel pump to seize, leading to stalling and an increased risk of a crash.

    Product
    VICTORY — VICTORY HAMMER EIGHT BALL, CROSS ROADS, HIGH BALL, VEGAS EIGHT BALL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment

    Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0899-2015·2015-01-07

    Smiths Medical Recalls Hypodermic Needles Due to Safety Sheath Failure

    Smiths Medical ASD, Inc. is recalling 10,000 units of Needle Pro Edge Safety Hypodermic Needles because the needle may not be captured in the safety sheath.

    Product
    Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0886-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk

    Roche Diagnostics is recalling 13,041 boxes of ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0892-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment

    Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0885-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk

    Roche Diabetes Care is recalling ACCU-CHEK Tender I infusion sets because tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0884-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk

    Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender I 13/80 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
    Category
    Medical Device
    Distribution
    Distributed nationwide