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.
BMW is recalling 2015 428i and 435i Convertibles because a programming error may cause the driver's front air bag to deploy at the wrong time, increasing injury risk in a crash.
Bon Appetizers, LLC is recalling approximately 10,429 pounds of chicken products because they contain peanut, a known allergen, which is not declared on the label.
Westinghouse Lighting is recalling about 5,000 glass shade holders sold at Home Depot because an incorrectly wired pull chain switch poses a risk of electrical shock.
Levels of Discovery is recalling about 150 Fly Boy Airplane Rockers because red wooden knobs on the steering console can detach, posing a choking hazard to young children.
M&M's World is recalling about 19,000 youth loungewear pants because they fail federal flammability standards for children's sleepwear, posing a burn risk.
Jardine Foods Inc is recalling D.L. Jardine's Texas Chili Bag O'Fixins Kit because ingredients contained undeclared peanuts.
Jardine Foods Inc is recalling 300 units of Four Banditos Sampler because ingredients contained undeclared peanuts.
Jardine Foods Inc is recalling Shotgun Willie's Texas Chili Seasoning because it contains undeclared peanuts.
Jardine Foods Inc is recalling 1,896 units of D.L. Jardine's Killer Barbecue Sauce because ingredients contained undeclared peanuts.
Jardine Foods Inc is recalling 3,576 units of Mesquite Barbecue Sauce because ingredients contained undeclared peanuts.
BMW is recalling specific 2005-2011 motorcycles because the rear wheel mounting flange may crack if bolts are over-tightened, potentially causing the wheel to detach.
Sagent Pharmaceuticals is recalling Atracurium Besylate Injection vials because FDA observations regarding aseptic and GMP practices at the manufacturing site may have impacted product sterility.
Richard Wolf Medical Instruments Corp. is recalling 83 I-Cart units because transformers may overheat, causing smoke and black plastic material to leak from the chassis.
Actavis Inc. is voluntarily recalling 29,405 cartons of Vancomycin Hydrochloride Capsules, USP, 250 mg, because the drug was found to be subpotent.
Jardine Foods Inc is recalling D.L. Jardine's Texas Chili Works due to undeclared peanuts in the ingredients.
Bendix is recalling specific TR-3 Inversion Air Brake Valves because incorrect dimensions may cause brakes to drag and overheat, increasing the risk of a wheel end fire.
Sagent Pharmaceuticals is recalling Atracurium Besylate Injection vials because FDA observations suggest potential impacts on product sterility.
Mack is recalling 2012-2015 Pinnacle trucks because the fifth wheel latch switch may be pushed accidentally, causing the trailer to disconnect.
Indian Motorcycle is recalling 2015 Scout models because a rear brake master cylinder defect may cause reduced or lost braking power, increasing crash risk.
Kalmar is recalling 311 model year 2014-2015 Ottawa T2 terminal tractors because a battery cable may detach, causing the engine harness to melt and increasing the risk of a fire.
Biosense Webster is recalling LASSO NAV Duo Loop eco Catheters due to reports of difficulty retracting and damage to the spine cover.
Actavis Inc. is voluntarily recalling 51,472 cartons of Vancomycin Hydrochloride Capsules, USP, 125 mg, because the drug is subpotent.
Zipline Medical is recalling Zip 8i Surgical Skin Closure Devices because the manufacturer's seal may be missing, compromising sterility assurance.
Philips Medical Systems is recalling Allura Xper X-Ray Angiographic systems due to a software error that may prevent the five-minute fluoroscopy audible signal from sounding.
Zipline Medical is recalling Zip 16 Surgical Skin Closure Devices because the manufacturer's seal may be missing, compromising sterility assurance.