State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2010-2014 Chevrolet Camaros because the ignition key may be accidentally knocked out of the run position by the driver's knee, potentially disabling airbags and power steering.
Honda is recalling specific 2003-2006 vehicles sold or registered in California due to a Takata air bag inflator defect that could rupture during deployment.
Volvo is recalling 2011-2015 VNL and 2014-2015 VNM trucks because the active braking component of the enhanced cruise control can become disabled, increasing crash risk.
Bellisio Foods is recalling Thai Kitchen Chicken Pad Thai frozen entrées because the packaging fails to list soy protein isolate, a known allergen.
General Motors is recalling 2013-2014 Cadillac ATS and 2014 CTS vehicles because the transmission shift cable may detach, causing unintended movement or rollaway.
Altec is recalling 258 aerial trucks because front torsion bar welds could fail, potentially causing vehicle instability and injury to the operator.
General Motors is recalling 2015 Chevrolet Silverado HD and GMC Sierra HD trucks because a power steering hose clamp may disconnect, potentially causing loss of steering and brake assist.
Reebok is recalling specific goalie throat collars because skate blades could penetrate the material, posing a risk of throat laceration. No injuries have been reported.
Linear LLC is recalling about 175,000 Personal Emergency Reporting System (PERS) transmitters because the batteries may fail to emit a low battery warning, leaving users unaware the device is not functioning.
General Motors is recalling 2014 Chevrolet Corvettes with optional sport seats because they do not meet injury protection specifications for unbelted young children.
General Motors is recalling 2011 Cadillac CTS vehicles because drive shaft vibrations may trigger roof rail air bags, increasing crash risk.
Dearborn Sausage Company is recalling approximately 3,660 pounds of slab bacon because the product contains hydrolyzed soy protein, a known allergen, that is not declared on the label.
James A. Kiley is recalling 2010-2013 Terex utility vehicles because oil may leak from the PTO pressure switch onto the exhaust, increasing fire risk.
MyNicNaxs, Inc. is recalling REDUCE WEIGHT FRUTA PLANTA Capsules because they contain undeclared phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Slim Xtreme Weight loss capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine, and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Magic Slim capsules because they contain undeclared active pharmaceutical ingredients and were marketed without an approved NDA or ANDA.
MyNicNaxs, Inc. is recalling Fruta BIO 400 mg capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicKnaxs is recalling weight reduction pills marketed without FDA approval because they contain undeclared phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi INSANE AMP'D dietary supplements because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Meizi Evolution Soft Gel Capsules because the product was marketed without an approved NDA/ANDA and contains undeclared active pharmaceutical ingredients.
MyNicNaxs, Inc. is recalling Jianfeijindan Activity Girl Capsules because they contain an undeclared sibutramine analog and were marketed without FDA approval.
Pure Edge Nutrition is recalling Bella Vi AMP'D UP weight loss capsules because they contain undeclared sibutramine and phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi BTrim MAX dietary supplements because they contain undeclared sibutramine and phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Meizitang Strong Version Botanical Slimming capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine.
Greenstone LLC is recalling 16,018 bottles of Venlafaxine HCl Extended-Release Capsules because a foreign capsule was found in a bottle from the same packaging campaign.