State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 344 Novae Sure-Trac equipment trailers from 2009-2012 because the tongue may crack and separate, increasing crash risk.
Land Rover is recalling 28,037 vehicles because the tire pressure monitoring system may fail to detect low pressure, increasing crash risk.
New England Wheels is recalling 2006-2014 Ford E-250 and E-350 vans with specific Ricon wheelchair lifts because the platform side plate may crack.
PACCAR is recalling Eaton V2020 Vane Pumps because the shafts could break, causing pump failure and a sudden loss of power steering assist.
Toys R Us is recalling Koala children's sandals because the butterfly wings can detach, posing a choking hazard to young children.
Zazou Scarves is recalling about 3,800 women's silk scarves because they fail to meet federal flammability standards, posing a risk of burn injury.
General Motors is recalling 106,307 vehicles from 2013-2014 because a contaminated chassis electronic module may cause an electrical short, leading to stalling and increased crash risk.
ICU Medical is recalling 100 units of ConMed Stat 2 flow controllers because they may deliver a significantly higher flow rate than intended.
ICU Medical is recalling STAT 2 Flow Controllers because they may deliver a significantly higher flow rate than intended.
Entegra is recalling 2015 Aspire and Anthem motorhomes because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Vapotherm is recalling 387 Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
ICU Medical is recalling specific IV administration sets because the Stat 2 flow controller may deliver a significantly higher flow rate than intended.
CareFusion is recalling 1,729 EnVe and ReVel ventilators because operator misconnection can damage the power connector, potentially shorting the power adapter.
ICU Medical is recalling STAT 2 Flow Controllers because they may deliver a significantly higher flow rate than intended.
Spacelabs Healthcare is recalling 222 patient monitors because they may fail to provide audible alarms in End Case mode, a defect missed in a previous recall.
Baxter Healthcare is recalling 148,632 bags of Potassium Chloride Injection because shipping cartons were incorrectly labeled and contained Gentamicin Sulfate Injection instead.
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during attachment or manipulation.
Peters Surgical is recalling 4,976 units of CARDIOXYL synthetic surgical sutures because a potential splitting of the surface treatment on thread ends was identified.
Vapotherm is recalling 22,042 Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
CareFusion is recalling approximately 318,280 heated infant breathing circuits due to a regulatory compliance risk involving a material change to the gas pathway.
Vapotherm, Inc. is recalling 1,005 units of Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Siemens is recalling 206 Artis zee and Artis zeego X-ray systems because radiation release can become blocked unnecessarily under certain circumstances.
Genesys Orthopedics Systems is recalling 642 Circular Lock Screws from the TiLock Pedicle Screw System because a portion of the lot was manufactured with stainless steel instead of the specified titanium alloy.
Alcon Research, Ltd. is recalling 2,462 Eye-Pak 7407 Tray Support Covers because insufficiently sealed peel pouches may compromise sterility.
Coach and Equipment is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.