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.
Hewlett-Packard is recalling specific AC power cords for notebook computers because they can overheat, posing a fire and burn hazard.
Agility Fuel Systems is recalling specific CNG fuel systems because a hose component may corrode and leak gas, increasing fire risk.
NABI is recalling 2012-2014 31LFW and 40LFW transit buses because CNG fuel tanks may be abraded by pressure relief devices, increasing fire risk.
Volkswagen is recalling 2013 Audi Q7 vehicles with 3.0L TDI engines because engine oil may leak into the brake booster, potentially causing a loss of power braking assist.
Jayco is recalling 2015 Seismic fifth wheel trailers because incorrect cargo capacity labels may lead to overloading, tire failure, and crashes.
Navistar is recalling FLTTRIKIT3 warning triangle kits manufactured between August 2012 and July 2014 because they may not reflect enough light to warn other drivers.
Cree is recalling approximately 10,000 LED high-bay luminaires because the tempered glass lens can break, posing a laceration hazard. No injuries have been reported.
Ace Bayou is recalling about 2.2 million bean bag chairs because zippers can open, allowing children to crawl inside and suffocate or choke on foam beads.
Ford is recalling 2014 Focus and C-Max vehicles manufactured in August 2014 due to incorrectly assembled steering gears that may cause loss of steering control.
APPA Fine Foods is recalling approximately 92,657 pounds of chicken Caesar salad kits due to possible Listeria monocytogenes contamination.
WilliamsRDM is recalling StoveTop FireStop Microhood units because the front canister may fall off and fail to suppress fires. No injuries have been reported.
SolarWorld is recalling solar systems installed with bare-copper grounding lugs due to corrosion risks that could cause electric shock, electrocution, or fire.
Super ARTHGOLD dietary supplement is being recalled because it contains undeclared prescription drugs and was marketed without FDA approval.
Thermo King is recalling specific 1100W, 1500W, and 2000W inverters sold between May and July 2014 because they may spark or overheat, posing a fire hazard.
Zimmer, Inc. is recalling 412 units of 23.5 Degree Rasp Handle Assemblies because the handle may fail to remain assembled to the rasp during use.
Zimmer, Inc. is recalling 412 nonsterile VER2 D8L Offset Rasp Handles because the handle may fail to remain assembled to the rasp during use.
Carestream Health is recalling 589 Kodak DirectView DR 7500 diagnostic x-ray systems because the x-ray tube assembly may detach from the overhead crane due to insufficiently tightened hardware.
Enhancement Medical is recalling 17,875 units of EXP-150 Injectable Gel because a production change altered the final gel weight. The recall covers all lots distributed in the US and Canada.
Zimmer, Inc. is recalling 23.5 Degree Rasp Handle Assemblies because the handle may fail to remain attached to the rasp during use.
Cardiovascular Systems, Inc. is recalling 48 Diamondback 360 Peripheral Orbital Atherectomy Systems because the saline sheath may crack or fracture, releasing particulate during use.
Medical Positioning Inc is recalling two Model # 1019 HUT tables due to a component defect that may cause the table to drop into the Trendelenburg position more rapidly than normal.
Teva Pharmaceuticals USA is recalling one lot of Carbidopa and Levodopa Tablets USP, 25mg/100mg, due to the potential for superpotent tablets.
Zimmer, Inc. is recalling 412 Double Offset Rasp Handles because the handle may fail to remain assembled to the rasp during use.
Zimmer, Inc. is recalling 412 Double Offset Rasp Handles because the handle may fail to remain assembled to the rasp during use.
Medical Positioning Inc is recalling 20 Rapid Response HUT tables because a defective component may cause the table to drop into the Trendelenburg position too rapidly.