State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Trucks North America is recalling 2017-2018 Freightliner Cascadia vehicles because brake lights may stay on after the pedal is released, increasing crash risk.
Chrysler is recalling 2019 Jeep Cherokee vehicles with 2.4L engines because improper transmission calibration may cause a stall, increasing crash risk.
Forest River is recalling 2019 Impression fifth wheels because side marker lights are misplaced, reducing visibility and increasing crash risk.
Forest River is recalling specific 2017-2019 motorhomes because a damaged rear module may cause marker, brake, or turn signal lights to stop working.
Harley-Davidson is recalling 177,636 motorcycles because a leaking clutch actuator may prevent disengagement, increasing crash risk.
Flushmate is recalling approximately 1.4 million pressure-assisted flushing systems because they can burst, posing impact and laceration hazards.
Hydrolevel is recalling HydroStat Model 3000 boiler controllers for Slant/Fin boilers because a malfunction can cause overheating and fire. No injuries or property damage have been reported.
Vista Railing Systems is recalling ProBuilt aluminum deck railing posts because they can separate from the base, posing a fall hazard. No injuries have been reported.
Charles Machine is recalling 2018 Ditch Witch trailers with vacuum excavators because the jib boom can become loose and swing outside the trailer while being towed.
Kikkerland is recalling wireless charger bedside pockets because they can overheat, posing fire and burn hazards. Three reports of smoke have been received, with no injuries reported.
BMW is recalling 2019 X5 xDrive40i vehicles because a short circuit in the Body Domain Controller may cause overheating and increase the risk of a fire.
Pfizer is recalling 94,752 bags of Magnesium Sulfate in Water for Injection because a single unit of Heparin was found inside a case.
Chrysler is recalling 21,104 Jeep Renegade vehicles because a fuel pump defect may cause a loss of fuel pressure and engine stall, increasing crash risk.
Sterilmed, Inc. is recalling 218 reprocessed Agilis Steerable Introducers because they may not meet endotoxin requirements. The devices were distributed in California, Colorado, Minnesota, and Washington.
Great Dane is recalling 2019 Champion Composite Plate dry freight trailers because they may have insufficient reflective tape, reducing visibility and increasing crash risk.
Bayer is recalling Codan Filters used in IV administration sets because the dust cap may generate particulate that enters the fluid path.
Neomed Inc is recalling NeoMed Enteral Feeding Tubes because the tethered plug may inadvertently open after closure, potentially compromising the device's seal.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because they may dispense insufficient sample volume without suppressing potentially incorrect results.
Whole Foods Market is recalling 365 Everyday Value White Corn Chips because they may contain undeclared milk. The affected products were distributed nationwide in the US and Canada.
Ortho-Clinical Diagnostics is recalling refurbished VITROS 5600 Integrated Systems because they may dispense insufficient sample volumes without suppressing potentially incorrect results.
AngioDynamics is recalling BioFlo Ports that were partially manufactured with the wrong sterile port assembly. The devices were distributed in Indiana.
Pfizer is recalling 7,777 bottles of Glipizide XL 5 mg tablets because rejected product was used in manufacturing, violating CGMP standards.
Instrumentation Laboratory is recalling 9,751 kits of HemosIL ReadiPlasTin due to potential imprecision and out-of-range quality controls.
Stryker Spine is recalling five AVS Aria Cage units because the anterior and posterior markers were placed on the incorrect sides of the device.
Implant Direct is recalling 217 units of Legacy Implant Closed-Tray Transfer components due to potential cap mislabeling. The correct part number is on the main vial label.