State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
REV Recreation Group is recalling specific 2015-2017 American Coach and Holiday Rambler motorhomes because interior step supports may be inadequately secured, creating an injury risk.
Porsche is recalling 2015-2017 Macan models because a faulty sensor may deactivate the front passenger air bag, increasing injury risk in a crash.
BMW is recalling 2011-2014 X5 and X6 vehicles because water and debris may cause the front driveshaft universal joint to fail, potentially affecting traction and increasing crash risk.
Polaris is recalling about 13,500 RZR and GENERAL off-highway vehicles due to engine misfires and brake issues that can cause fires and burns.
Porsche is recalling 2017 911 and 718 Boxster vehicles because the windshield may not be properly bonded, increasing injury risk in a crash.
Kids II is recalling Oball Rattles because the plastic disc can break, releasing small beads that pose a choking hazard to young children.
Subaru is recalling 2017 Impreza vehicles because a software problem may cause the rearview camera display to malfunction, increasing crash risk.
Porsche is recalling 2016-2017 911 and 718 models because the passenger air bag inflator may fail to ignite, increasing injury risk in a crash.
One World Technologies is recalling Ryobi 8amp Electric Jet Fan Blowers because the internal plastic fan can break, discharging blades that pose a laceration hazard.
Goodman is recalling approximately 210,000 air handler units because the pull-out disconnects may fail to disable power, posing an electrical shock hazard to individuals servicing the equipment.
Volkswagen is recalling 2017 Beetle and Jetta GLI vehicles because incorrect tire information labels may cause operators to overload the vehicle, increasing crash risk.
Volkswagen is recalling 2017 Jetta vehicles because incorrect tire information labels may lead to vehicle overloading, increasing crash risk.
New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.
Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.
Philips Lighting is expanding a recall of about 256,000 Metal Halide Lamps because the outer bulbs can shatter, posing fire and laceration risks.
REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.
Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.
Pier 1 Imports is recalling about 363,000 glass knobs sold in the U.S. because they can break and cause lacerations.
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.
Hostess Brands is recalling Holiday White Peppermint Twinkies because an ingredient may be contaminated with Salmonella. The product was distributed nationwide.
Tosoh Smd Inc is recalling 34 units of Reporting Software for the G8 analyzer because power outages cause the software to shut down.
Sandoz Inc. is recalling Transderm Scop patches because the outer carton contains incorrect instructions for cutting the patch.