State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Winnebago is recalling 2012-2016 Era recreational vehicles because certification labels list incorrect front tire inflation pressures, which could lead to tire failure.
Oxysure Systems is recalling 1,005 Model 615 oxygen cartridges because they do not meet FDA flow rate standards.
Ameritrans is recalling 2015 225 vehicles because the back-up camera may display reversed images, increasing the risk of a crash.
Boehringer Ingelheim is recalling 358,647 Combivent Respimat inhalers because the delivery system may fail to spray properly.
Siemens is recalling ACUSON S2000 and S3000 ultrasound systems with Virtual Touch IQ due to a potential measurement alignment error.
Hardy Diagnostics is recalling MDR Acinetobacter and other diagnostic media because they lack FDA 510(k) clearance.
Hardy Diagnostics is recalling several microbiology media products, including BEA Broth with Vancomycin, because they lack FDA 510(k) clearance.
Hardy Diagnostics is recalling specific lots of MacConkey Agar and other diagnostic media because they lack FDA 510(k) clearance.
Hardy Diagnostics is recalling several microbiology media products, including BEA Agar with VGA, because they lack FDA 510(k) clearance.
Synthes (USA) Products LLC is recalling 31 pre-bent maxillary plates due to potential incorrect laser etch denoting orientation.
McKesson Technologies is recalling Paragon Laboratory Management software versions 12.1 and 12.1.1 because the Final Cumulative Report may display incorrect data when used with Microsoft SQL Server 2012.
Philips is recalling 697 MRI patient monitoring systems because the labeling inaccurately lists endotracheal as a valid body temperature application site for the FlexTEMP sensor.
Hardy Diagnostics is recalling several clinical culture media products, including BHI with Ciprofloxacin, because they lack FDA 510(k) clearance.
Philips is recalling four Brilliance CT 64-channel systems due to software errors affecting image quality, dose control, and heart rate measurements.
Acon Laboratories is recalling 1,283 Mission Breath Alcohol Detector kits due to a labeling amendment. The devices are distributed nationwide.
Hardy Diagnostics is recalling several microbiological media products, including BEA Agar with Vancomycin, because they lack FDA 510(k) clearance.
Hardy Diagnostics is recalling VRE Broth and other diagnostic media because they lack FDA 510(k) clearance. The products were distributed in the U.S. and Canada.
New Flyer is recalling specific 2014-2015 NABI transit buses because pressure relief devices may fail to vent gas, increasing the risk of tank explosion, fire, and injury.
Emerson is recalling specific Fisher Pressure Relief Valves used in cargo tank trailers. The valves may restrict flow during a fire, increasing the risk of tank explosion.
Nissan is recalling 46,846 Altima and Maxima vehicles because an improperly installed o-ring may cause fuel to leak during a crash, increasing fire risk.
Volkswagen is recalling specific 2010-2014 models because debris may damage the air bag clock spring, preventing the driver's air bag from deploying in a crash.
John Deere is recalling specific riding lawn tractors because a brake arm can fail, posing a crash hazard that could result in serious injury or death.
Forest River is recalling 2015-2016 Cedar Creek Silver Back recreational vehicles because the gross vehicle weight rating on the certification label is incorrect.
Manhattan Group is recalling My Snuggly Ellie Activity Toys because the wooden ring can break into small pieces, posing a choking hazard to young children.
Good Food Made Simple is recalling approximately 3,574 pounds of turkey and pork breakfast products that were distributed in California without U.S. inspection.