State
73,737 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Valeant Pharmaceuticals is recalling 206 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, meaning the drug may not release properly.
Ottobock is recalling PushValve upper parts because some installed valve inserts have a diameter smaller than the specification.
Valeant Pharmaceuticals is recalling 1,023 bottles of Cardizem CD (diltiazem hydrochloride) 120 mg capsules because they failed to meet dissolution specifications.
Valeant Pharmaceuticals is recalling 23,884 bottles of Diltiazem HCl CD capsules because they failed dissolution specifications, potentially affecting drug release.
Dr. Reddy's Laboratories is recalling Esomeprazole Magnesium 40mg capsules because they may contain brown pellets.
Akorn Inc. is recalling 30,794 bottles of COSOPT Ophthalmic Solution because the product failed stability specifications for opalescence.
Luminex Corporation is recalling Verigene BC-GP Utility Kits because they were incorrectly labeled with Amplification Tray labels.
Keystone is recalling 2019 Crossroads Redwood recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.
Academy Sports + Outdoors is recalling Outdoor Gourmet Turkey Keg turkey fryers because the spout can leak oil, posing a fire hazard.
Kia is recalling 2015-2018 Sedona vehicles with manual front passenger seats because a wiring harness may break, potentially allowing the airbag to deploy and injure a child.
Spartan Motors is recalling 2018-2019 Utilimaster Truck Body and Velocity vehicles because backup camera monitors may display reversed images, increasing crash risk.
Keystone is recalling 2019 Bullet Crossfire recreational trailers because the rear-wall spare tire carrier may detach, creating a road hazard.
Autocar is recalling 2008-2019 Xpeditor vehicles because undersized brake chambers may allow the truck to roll when parked, increasing crash risk.
Kia is recalling 2011-2012 Sportage vehicles because the engine oil pan may leak, potentially causing engine damage, fire, or stalling.
Eldorado is recalling 2012-2018 Goshen shuttle buses because a wheelchair lift cam may fail, allowing the platform to rise too high and risk injury.
Oshkosh is recalling 2014-2019 S-Series Glider vehicles because incorrectly placed strobe lights may confuse other drivers and increase crash risk.
Ford is recalling 2019 Fusion Energi Hybrid vehicles because they may not adequately protect against high voltage contact during normal operation.
New Flyer is recalling 172 transit buses because the rooftop emergency escape hatch glass may shatter in extreme cold, posing an injury risk to passengers.
Toyota is recalling 2019 Camry Hybrid and Avalon Hybrid vehicles because the fuel filler pipe may not be properly connected, posing a fire risk.
Ferrari is recalling 2,150 vehicles because a cracked fuel vapor separator may leak fuel, increasing the risk of fire.
PurpleAir is recalling PowerStream power supply units for air sensors because they can overheat, posing fire and burn hazards. No injuries have been reported, but 27 reports of sparks or smoke were received.
CVB is recalling LUCID Folding Mattress-Sofas because they fail to meet the mandatory federal flammability standard for mattresses, posing a fire hazard.
Ferrari is recalling 2017-2019 GTC4Lusso and 2018-2019 GTC4Lusso T vehicles because tension on the door lock mechanism may prevent doors from opening with the external handle.
Smiths Medical is recalling Portex 550 ml Sterile Water Humidifiers because leaking containers may compromise sterility, potentially exposing patients to infectious agents.
Smiths Medical is recalling Portex 350 ml Sterile Water Humidifiers because leaking containers may expose patients to infectious agents.