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.
LiquidSpring is recalling specific aftermarket suspension units for Ford and Chevrolet chassis because a mounting bracket may fail, allowing the fluid tank to separate and become a road hazard.
Ford is recalling 2012-2014 Edge, MKX, Taurus, MKS, Flex, and MKT vehicles because a halfshaft may disengage, causing loss of power or vehicle roll-away.
NxStage Medical is recalling dialysate sacks used with the PureFlow SL system because they contain aluminum levels exceeding internal specifications.
Biomet, Inc. is recalling one unit of a Discovery Elbow prosthesis because the surface finish differs from specifications, potentially causing pain requiring surgery.
General Motors is recalling 2014 Buick Regal, Cadillac XTS, Chevrolet Camaro, and Chevrolet Impala vehicles because improperly torqued fasteners may cause steering components to separate, increasing crash risk.
Ford is recalling 2011-2014 F-59 commercial chassis vehicles because a short circuit in the electrical system may cause a fire.
Chrysler is recalling 2014 Jeep Cherokee, Ram 1500, and 2015 Chrysler 200 vehicles because an insufficient weld may cause rear shocks to detach, potentially damaging tires or reducing braking.
Sutphen is recalling one 2013 Minitower fire truck because seat belt buckles may fail to release, potentially hindering emergency egress.
Zynex Medical is recalling 1,461 IF 8000 devices because a malfunction can cause them to stop working or overheat, posing a burn risk.
NxStage Medical is recalling 2,711 cases of dialysate sacks because aluminum levels exceeded internal specifications.
Pfizer is recalling Pristiq 50 mg extended-release tablets because a 100 mg tablet was found in a bottle labeled for 50 mg.
Siemens Healthcare is recalling ADVIA Acid/Base Reagent 1 and 2 Kits because trace metal contamination caused the acid bottles to swell.
All Power America is recalling about 10,000 single stage snow throwers because a corroded carburetor needle can cause fuel leaks, posing a fire hazard.
Siemens is recalling 317 StreamLAB Analytical Workcells because protruding pins on the Input/Output Module have contributed to trip and fall incidents.
General Motors is recalling specific 2012-2014 Buick and Chevrolet vehicles because insulation on the engine block heater cord can damage in cold weather, exposing wires.
NxStage Medical is recalling dialysate sacks with concentrate due to aluminum levels exceeding internal product specifications.
Elekta, Inc. is recalling MOSAIQ oncology information system software because it fails to recalculate agent volume when users change the ordering dose.
NxStage Medical is recalling dialysate sacks with concentrate due to aluminum levels exceeding internal product specifications.
Nellcor Puritan Bennett is recalling 104 Puritan Bennett 840 Ventilators due to reports of loss of graphical user interface display information while the device continues to provide breath support.
SteriGear is recalling 110,560 urinary drain bags because the valve can close and create negative pressure, potentially blocking urine flow.
Western / Scott Fetzer Company is recalling Model RG3000 and RG4000 Series Valve Integrated Pressure Regulators (VIPR) because they may separate from aluminum cylinders.
Porter-Cable is recalling fixed-base production routers and bases because the handles lack insulation, posing an electrical shock risk. No injuries have been reported.
Siemens is recalling Dimension LOCI Troponin I Calibrators because they may cause a 24% upward shift in test results.
Integra LifeSciences is recalling 61 units of Accell Evo3C Demineralized Bone Matrix because they were incorrectly packaged in boxes for a different product, creating a risk of improper surgical use.
Teleflex Medical is recalling RUSCH LaserTube tracheal tubes because the label failed to print a specific caution statement regarding natural rubber latex.