The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58701–58725 of 73856

  • LowFDA (Drugs)·D-1227-2014·2014-04-16

    Novartis Recalls Ritalin Tablets Due to Incorrect Medication Guide Labeling

    Novartis is recalling Ritalin tablets because the attached Medication Guide contained information for the sustained-release version. The recall is limited to a specific lot distributed nationwide and in Puerto Rico.

    Product
    RITALIN — RITALIN (METHYLPHENIDATE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1228-2014·2014-04-16

    Novartis Recalls Ritalin Tablets Due to Incorrect Medication Guide Labeling

    Novartis is recalling 10,781 bottles of Ritalin 20 mg tablets because the attached Medication Guide contained information for Ritalin SR instead of Ritalin Tablets.

    Product
    RITALIN — RITALIN (METHYLPHENIDATE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1226-2014·2014-04-16

    Hospira Recalls Demerol Ampoules Due to Missing Container Labels

    Hospira Inc. is recalling 237,850 ampoules of Demerol (meperidine HCL) because the immediate container labels are missing. The recall is nationwide.

    Product
    Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V182000·2014-04-15

    Volkswagen Recalls 2014 Models for Transmission Fluid Leak Fire Risk

    Volkswagen is recalling 2014 Jetta, Beetle, and Passat vehicles because leaking transmission fluid could contact hot surfaces and cause a fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT, JETTA, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E017000·2014-04-15

    Carrier Trailer Refrigeration Units Recalled for Wiring Fire Risk

    Carrier is recalling specific trailer refrigeration units and part kits because a bolt may abrade wiring, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·015-2014-EXP·2014-04-14

    Nutriom LLC Recalls Dried Egg Products Due to Possible Salmonella Contamination

    Nutriom LLC is recalling dried egg products due to possible Salmonella contamination. The recall includes an additional 82,884 pounds of product.

    Product
    Washington Firm Recalls Dried Egg Products Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V195000·2014-04-11

    Open Range LF319 Trailer Recall for Short Kitchen Gas Line

    Open Range is recalling 2014 LF319 fifth wheel trailers because a short gas line in the kitchen slideout may leak when expanded, increasing fire risk.

    Product
    OPEN RANGE — OPEN RANGE LF319
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V177000·2014-04-11

    Mercedes-Benz Recalls C-Class Vehicles for Tail Light Electrical Defect

    Mercedes-Benz is recalling 2008-2011 C300, C350, and C63 AMG vehicles because a poor electrical ground may cause tail lights to dim or fail, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C350, C300, C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V171000·2014-04-10

    GM Recalls Vehicles for Ignition Key Removal Defect

    General Motors is recalling specific Saturn, Chevrolet, and Pontiac vehicles because the ignition key can be removed while the engine is running, creating a rollaway risk.

    Product
    SATURN — SATURN, CHEVROLET, PONTIAC ION, COBALT, SOLSTICE, HHR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V176000·2014-04-10

    BMW Recalls 2010-2012 Models for Engine Bolt Failure Risk

    BMW is recalling approximately 156,137 vehicles because VANOS housing bolts may loosen or break, potentially causing the engine to stall and increasing crash risk.

    Product
    BMW — BMW 128I, 135I, 328I, 535I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V189000·2014-04-10

    MV Agusta Recalls 2014 Motorcycles Due to Swingarm Bolt Failure Risk

    MV Agusta is recalling 223 model year 2014 motorcycles because a swingarm bolt may fail, increasing the risk of a crash.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800, BRUTALE RR, F3 675, RIVALE 800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14729·2014-04-10

    Whalen Recalls Stainless Steel Tool Chests Due to Laceration Hazard

    Whalen is recalling approximately 20,000 stainless steel tool chests sold at Costco due to a sharp metal edge on the right door that poses a laceration hazard.

    Product
    Stainless steel tool chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V190000·2014-04-10

    Forest River Recalls 2014 Vibe Travel Trailers for Incorrect Certification Labels

    Forest River is recalling 164 model year 2014 Vibe travel trailers because the Federal Certification Label lists incorrect tire and weight information, which could lead to overloading and tire failure.

    Product
    VIBE — VIBE VCT6504, VCT6501, VCT6502, VCT6503
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E015000·2014-04-10

    Villa Recalls Defective Seat Belts in Jayco, Tiffin, and American Coach RVs

    Villa International is recalling specific driver and passenger seats used in 2014-2015 Jayco, Tiffin, and American Coach recreational vehicles because the seat belt attachment may be incorrect and the belt may fray, reducing its strength.

    Product
    JAYCO — JAYCO, TIFFIN, AMERICAN COACH ENTEGRA CORNERSTONE, ZEPHYR, ALLEGRO, AMERICAN TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14146·2014-04-10

    BedHead Recalls Children's Pajamas for Flammability Standard Violations

    BedHead Pajamas Inc. is recalling about 800 children's two-piece pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.

    Product
    Children's Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V168000·2014-04-09

    Toyota and Pontiac Vehicles Recalled for Driver Airbag Cable Defect

    Toyota and General Motors are recalling specific 2006-2010 vehicles because a steering cable defect may prevent the driver's airbag from deploying in a crash.

    Product
    TOYOTA — TOYOTA, PONTIAC TACOMA, YARIS, VIBE, COROLLA MATRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1189-2014·2014-04-09

    FDA Recalls HydrOXYzine HCl Tablets Due to Unapproved Ingredient Source

    American Health Packaging is recalling HydrOXYzine HCl 50 mg tablets because the active ingredient came from an unapproved source.

    Product
    HydrOXYzine HCl Tablets, USP 50 mg, 100 Tablet Blister, Rx only Mfd by: KVK-TECH, INC. Newtown, PA 18940, NDC 68084-255-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V169000·2014-04-09

    Toyota Recalls Yaris and Scion xD for Seat Rail Spring Defect

    Toyota is recalling 2006-2010 Yaris and 2008-2010 Scion xD vehicles because seat rail springs may break, potentially allowing the seat to move during a crash.

    Product
    TOYOTA — TOYOTA, SCION YARIS, XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1320-2014·2014-04-09

    Merit Medical Systems Recalls Non-Sterile Custom Syringe Kits

    Merit Medical Systems is recalling 15 syringe kits labeled as sterile but not sterilized. The products were distributed in the US, Thailand, and Hong Kong.

    Product
    Merit Custom Syringe Kit, Convenience Kit, I.R. Embolization Pack, K02-01010A, Sterile EO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1298-2014·2014-04-09

    Draeger PS500 Power Supply Unit Recalled Due to Reduced Battery Capacity

    Draeger Medical Systems is recalling 1,544 PS500 Power Supply Units because the battery capacity did not last as long as expected.

    Product
    Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Critical Care (Evita Infinity V500), Evita V500 and /or Babylog VN500 Ventilators, used for ventilation during short term transport of patients within a hospital.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1725-2014·2014-04-09

    Unilever Recalls Popsicle Ice Pops Due to Potential Milk Exposure

    Unilever is voluntarily recalling specific Popsicle ice pop boxes because they may have been exposed to milk, an ingredient not listed on the label.

    Product
    Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs, NJ 07632 USA UPC 077567121301
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V179000·2014-04-09

    Winnebago Recalls 2014-2015 Motorhomes for Brake Hose Defect

    Winnebago is recalling specific 2014-2015 motorhomes because a manufacturing defect may have damaged brake hoses, potentially causing fluid leakage and reduced braking performance.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, ITASCA VIVA, TREND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1311-2014·2014-04-09

    Zoll Medical Defibrillators Recalled for Continuous Device Reset Loop

    Zoll Medical is recalling 3,169 defibrillator/pacemaker/monitor units because they may latch in a continuous reset loop, rendering them unusable.

    Product
    Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
    Category
    Medical Device
    Distribution
    Distributed nationwide