State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Huish Outdoors is recalling Oceanic and Hollis scuba diving regulators because they can restrict airflow at low tank pressures, posing a drowning hazard to divers.
Forest River is recalling 2019 Wildwood and Salem trailers because a wiring defect may prevent brakes from engaging if the trailer detaches.
Volkswagen Group of America is recalling 2013-2015 Audi S8 and A8 vehicles because a fuel supply line may leak, increasing fire risk.
Keystone is recalling 2019 Summerland recreational trailers because the Federal Identification Label lists an incorrect tire rim size, which could lead to improper rim replacement.
Spartan Motors is recalling 2009-2018 Gladiator and MetroStar emergency vehicles because internal corrosion in the fire water pump solenoid may cause loss of water pressure, increasing injury risk.
Mazda is recalling 2018 CX-5 vehicles because side curtain air bags may not unfold properly in a crash, increasing injury risk.
Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because non-flexible wiring in the bedroom slide-out may damage and cause a fire.
E-One is recalling 2016-2017 Cyclone II emergency vehicles because stress fractures in the aerial ladder tubing could cause failure and injure the bucket occupant.
Triple E RV is recalling 2017-2018 Wonder recreational vehicles because water can corrode wiring in the trailer tow module, potentially causing electrical shorts, fire, or crash risks.
Ricon is recalling S-Series and K-Series wheelchair lifts because a component may fail, allowing the platform to rise too high and increase injury risk.
Achieva Rubber Corp. is recalling specific Innova Ultra Runner tires that fail to meet Federal Motor Vehicle Safety Standard 119, posing a crash risk.
BMW is recalling 2018 X3 xDrive30i and M40i vehicles because rear turn signals may display incorrect colors, potentially confusing other drivers.
Syncro is recalling Hayes Sway Master units that may disable trailer brakes, increasing crash risk.
Inopak Ltd is recalling Option Systems Antibacterial Foaming Hand Wash because FDA analysis found out-of-specification microbial counts.
TRW is recalling air bag control units in certain Hyundai and Kia vehicles because electrical overstress may prevent air bags and seat belt pretensioners from deploying in a crash.
Shadow Holdings DBA Bocchi Labs is recalling the Acne Shave 3 Step Shaving System due to CGMP deviations that may result in bacterial contamination.
Medline Industries is recalling specific lots of READYFLUSH PROTECT flushable personal cleaning cloths because of microbial contamination in a non-sterile product.
Allergan is recalling Taytulla softgel capsules because the tablets are out of sequence. This affects 168,768 blister cards distributed nationwide.
Shadow Holdings DBA Bocchi Labs is recalling Acne Shave Shave Cream due to CGMP deviations that may allow bacterial contamination.
PharMEDium Services is recalling 2,800 hydromorphone syringes nationwide because some units were found to be superpotent or subpotent.
Shadow Holdings DBA Bocchi Labs is recalling X-Jow Pain Gel because CGMP deviations may have allowed bacterial contamination.
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Gentamicin Flex reagent cartridges because they may produce inaccurate test results at the low end of the measurement range.
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista Gentamicin Flex reagent cartridges because they may produce inaccurate results at low concentrations.
Shimadzu Medical Systems is recalling 17 Sonialvision Safire II angiographic x-ray systems because the irradiation time and integral dose displays may reset to zero during serial radiography.