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.

58201–58225 of 73856

  • ModerateFDA (Devices)·Z-1653-2014·2014-06-04

    Siemens Recalls ADVIA Centaur TSH3 Ultra Ready Packs Due to Interference

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur TSH3 Ultra Ready Packs because samples containing fluorescein may interfere with assay results.

    Product
    ADVIA Centaur Systems TSH3 Ultra Ready Pack, 100 test Catalog Number: 06491072; Siemens Material Number: 10282378. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1353-2014·2014-06-04

    PediaCare Day & Night Cold Syrup Recalled for Precipitate

    Prestige Brands Holdings is recalling PediaCare Day & Night Cold syrup bottles due to the presence of precipitate.

    Product
    PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold (dextromethorphan HBr 5 mg and Phenylephrine HCl 2.5 mg) and NIGHTTIME MULTI-SYMPTOM Cold (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL oz (118 mL) bottles, one each of DAYTIME MULTI-SYMPTOM…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1352-2014·2014-06-04

    PediaCare Nighttime Cold Syrup Recalled for Diphenhydramine Precipitate

    Prestige Brands Holdings is recalling PediaCare Nighttime Multi-Symptom Cold syrup due to the presence of diphenhydramine precipitate in the solution.

    Product
    PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold, (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL OZ (118 mL), Distributed by Medtech Products, Inc., Tarrytown,NY ---- UPC 814832013544
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V291000·2014-06-02

    Jaguar Recalls 2013-2014 XF Models Due to Brake Pipe Wear

    Jaguar is recalling 2013-2014 XF vehicles because the rear brake pipe may wear and leak fluid, increasing crash risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E035000·2014-06-02

    Roush Propane Fuel System Conversion Kits Recalled for Leak Risk

    Roush CleanTech is recalling propane fuel system conversion kits for Ford vans due to a potential leak at the fuel line fitting that could cause a fire.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V292000·2014-06-02

    Jaguar Recalls 2013 XJ Vehicles Due to Airbag Software Defect

    Jaguar is recalling 2013 XJ vehicles because generic software in the Restraints Control Module may prevent the airbag system from operating correctly, increasing injury risk in a crash.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V289000·2014-05-30

    Kia Recalls 2014 Cadenza Vehicles Due to Wheel Fracture Risk

    Kia is recalling 2014 Cadenza vehicles with 19-inch non-chrome aluminum wheels because they may fracture from impacts, increasing crash risk.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E028000·2014-05-29

    Ford Recalls All-Weather Floor Mats for Interference with Accelerator Pedal

    Ford is recalling all-weather driver-side floor mats for 2006-2011 Ford, Mercury, and Lincoln vehicles because they may shift and interfere with the accelerator pedal.

    Product
    LINCOLN — LINCOLN, MERCURY, FORD MKZ, MILAN, FUSION, ZEPHYR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14196·2014-05-29

    Trident Recalls Pool UV Sanitation Systems Due to Fire Hazard

    Trident is recalling Series 2 ultraviolet pool sanitation systems because electrical arcing can cause them to catch fire. Consumers should unplug the units and contact Trident for a free repair kit.

    Product
    Trident Series 2 Ultraviolet Sanitation Systems for pools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V286000·2014-05-29

    Ford Recalls 2011-2013 Explorers for Electric Power Steering Defect

    Ford is recalling 2011-2013 Explorers because an intermittent connection in the electric power steering gear can cause a loss of power steering assist, increasing crash risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V287000·2014-05-29

    Terex Aerial Devices Recall for Frame Crack Risk

    Terex is recalling 2006-2014 TLM series aerial devices installed on Ford F550 vehicles due to a potential frame crack that could cause loss of control.

    Product
    TEREX — TEREX AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14195·2014-05-29

    Sunbeam Recalls Holmes Ceramic Heaters Due to Fire Hazard

    Sunbeam is recalling about 151,600 Holmes ceramic heaters because they can overheat and pose a fire hazard. Consumers should stop using the units and contact Sunbeam for a refund.

    Product
    Holmes Ceramic Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V282000·2014-05-29

    Mazda Recalls Tribute Vehicles for Steering Assist Software Defect

    Mazda is recalling 2008-2011 Tribute vehicles because a steering sensor may fail, causing the electric power steering assist to disengage.

    Product
    MAZDA — MAZDA TRIBUTE, TRIBUTE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V283000·2014-05-29

    Peterbilt Trucks Recalled for Side Air Bag Warning Light Defect

    PACCAR is recalling 2010-2015 Peterbilt trucks because a blown fuse can disable the side air bag without triggering a warning light, increasing injury risk.

    Product
    PETERBILT — PETERBILT 365, 388, 348, 384
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V284000·2014-05-29

    Ford Recalls 2008-2011 Escape and Mercury Mariner for Steering Defect

    Ford is recalling 2008-2011 Escape and Mercury Mariner vehicles because the steering torque sensor may fail, causing loss of power steering assist.

    Product
    MERCURY — MERCURY, FORD MARINER, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1539-2014·2014-05-28

    Fisher & Paykel Recalls Infant Nasal CPAP Prongs for Detachment Risk

    Fisher & Paykel Healthcare is recalling infant nasal CPAP prongs and starter kits because the prongs may detach from the tubing, interrupting therapy.

    Product
    Infant Nasal CPAP (continuous positive airway pressure) Prong, Nasal. CPAP Prongs (10 pack): Model No. BC3020-10, BC3520-10, BC4030-10, BC4540-10, BC5040-10, BC5050-10, BC5550-10, BC5560-10, BC6060-10, BC6070-10, BC6570-10. Bubble CPAP Starter Kits: Model No. BC461-SK…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1328-2014·2014-05-28

    Pfizer Recalls Effexor XR Capsules Due to Foreign Tablet Contamination

    Pfizer is recalling specific lots of Effexor XR 150 mg capsules because a foreign Tikosyn capsule was found in a bottle.

    Product
    Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC 0008-0836-21) UPC 3 0008-0836-21 7; b) 90-count Unit of Use bottles (NDC 0008-0836-22) UPC 3 0008-0836-22 4; Rx only, Distributed by Wyeth Pharmaceuticals Inc., A…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1333-2014·2014-05-28

    Herbal Give Care Recalls Esbelder Fem Supplement for Undeclared Sibutramine

    Herbal Give Care Llc is recalling Esbelder Fem Mezcla con L-Carnitina because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.

    Product
    Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio,30 capsule bottle, Hecho en Mexico: Soluciones HGC S. de R.L. de C.V. Av. Independencia #1060 Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7502011000251
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1329-2014·2014-05-28

    Esbelin Siloutte Mezcal Herbal Recalled for Undeclared Sibutramine

    Herbal Give Care Llc is recalling Esbelin Siloutte Mezcal Herbal because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.

    Product
    Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio, 30 capsule bottle, Hecho En Mexico Por: Soluciones HGC S. de R.L. de C.V. Av. Independicia #1016 Frac. La Rinconada Aguascalientes, Ags. Mex C.P. 20136, UPC 7502011000060
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1346-2014·2014-05-28

    Naturect Capsules Recalled for Undeclared Tadalafil Ingredient

    Tendex is recalling Naturect Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.

    Product
    NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Distributed by P-Boost, Los Angeles, CA 900466
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1332-2014·2014-05-28

    Esbelder Man Herbal Blend Recalled for Undeclared Sibutramine

    Herbal Give Care Llc is recalling Esbelder Man Herbal Blend because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.

    Product
    Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement, 30 capsule bottle, Made in Mexico: Soluciones S. de R.L. de C.V. Av. Independencia #1060 Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7502011000275
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1330-2014·2014-05-28

    Herbal Tea Recalled for Undeclared Sibutramine and Related Compounds

    Herbal Give Care Llc is recalling Esbelin Siloutte Te herbal tea because it contains undeclared sibutramine and related compounds, making it an unapproved new drug.

    Product
    Esbelin Siloutte Te, Suplemento Alimenticio, herbal tea in a gold foil/plastic zip-lock pouch. Hecho en Mexico Por: Herbal Give Care, Av Independencia # 1016, Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7562684652553
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1327-2014·2014-05-28

    PRO ArthMax Dietary Supplement Recalled for Unapproved Active Ingredients

    Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.

    Product
    PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA
    Category
    Drug
    Distribution
    Distributed nationwide