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.
Daimler Trucks North America is recalling 2015 Thomas Built Buses Saf-T-Liner HDX school buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Arctic Cat is recalling approximately 40,000 model year 2008 and 2009 ATVs because front gear case components can fail, posing a crash hazard.
FDA recalls 133,930 pairs of Kendall defibrillation electrodes because they are not compatible with specific Philips AED models.
Gel Spice Co. is recalling Fresh Finds ground black pepper due to potential Salmonella contamination. Consumers should stop using the product.
FDA recalls 317,550 pairs of defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Bumble Bee Foods is recalling specific codes of Chipotle Albacore Tuna pouches because seal defects could allow contamination by spoilage organisms or pathogens.
Siemens Healthcare Diagnostics is recalling approximately 4,200 external power supply adapters for the Clinitek Status+ urine analyzer due to damage that can cause electric shock.
Coviden LLC is recalling 9,850 pairs of Medi-Trace Cadence defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Elgin is recalling 2012-2014 Broom Badger sweeper trucks because a hydraulic oil cooler fan may fail, causing overheating and potential vehicle fire.
Hospira is recalling 109,110 vials of Lidocaine Hydrochloride Injection because the product was discolored and contained visible particulates.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
The FDA is recalling 330 pairs of MediChoice Multifunction Electrodes because they are not compatible with certain Philips AED models.
Covidien is recalling Philips HEARTSTART Multifunction Electrode Pads because they are not compatible with Philips FR3 or FRx AEDs.
Neely Coble is recalling 52 Isuzu NQR vehicles with dual steering modifications due to a potential steering column separation risk.
Intuitive Surgical is recalling 1,034 EndoWrist Stapler 45 instruments because they may not be removable from tissue.
FDA recalls 31,590 pairs of Kendall defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Bumble Bee Foods is recalling Sun Dried Tomato pouches because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna due to seal defects that could allow contamination by spoilage organisms or pathogens.
Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer because they are damaged and can cause electric shock.
Merge Healthcare is recalling eFilm Workstation versions 4.0 and 4.0.1 because a software defect may cause users to select the wrong patient study when using the thumbnail panel.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Biomet is recalling six Discovery Elbow Humeral Trials that were incorrectly manufactured as left-sided but etched as right-sided.
Gulf States Toyota is recalling 142 model year 2015 Toyota Tacoma vehicles because they may have incorrect load carrying capacity labels, which could lead to vehicle overload.