State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GD Midea is recalling approximately 3.4 million dehumidifiers sold in the U.S. because they can overheat, smoke, and catch fire, posing serious fire and burn hazards.
Roche is recalling 9,014 cobas e411 Immunoassay Analyzers because the sharp edge of the sample rack tray center guide rail caused four reported injuries.
Roche is recalling Modular Analytics Combination Systems because a sharp edge on the sample rack tray caused four reported injuries. The cleaning procedure has been revised to clarify the process.
Roche is recalling 9,014 cobas 6800/8800 systems because a sharp edge on the sample rack tray caused four reported injuries.
Roche is recalling cobas p 612 Pre-Analytical Instruments because the sharp edge of the sample rack tray center guide rail caused four reported injuries.
Roche is recalling 9,014 RSD 800A Aliquoting System calculator/data processing modules because four reports of injury were received from the sharp edge of the sample rack tray.
Chrysler is recalling 2017 Jeep Cherokee vehicles because improper welds may prevent the driver's knee air bag from inflating properly.
Nova Medical is recalling 1,380 Journey Rolling Walkers because screws holding the side supports can loosen and fall out.
Hospira is recalling Symbiq One Channel Infusers because a white screen during KVO titration may allow premature programming, potentially causing therapy delays and significant injury.
Volvo is recalling 74,027 vehicles because the front passenger seat belt buckle may separate, increasing crash injury risk.
Roche is recalling VS II Aliquoter System calculator modules because a sharp edge on the sample rack tray caused four reported injuries.
Wilton Brands is recalling 22,182 bottles of Gold Airbrush Color due to potential contamination with mold, yeast, or bacteria.
Wilton Brands is recalling Wilton Pearl Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Hospira is recalling Symbiq Two Channel Infusers because a white screen error during KVO titration could delay therapy and cause significant injury.
Running Trainer is recalling 240 Bionic Runner bicycles because the pedals can detach, posing a fall hazard to riders.
Pier 1 Imports is recalling approximately 140,000 glass knobs sold in the U.S. because they can break during use, posing a risk of laceration.
Wilton Brands is recalling 16,188 bottles of Blue Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.
Boehringer Ingelheim is recalling 2,562 bottles of 75 mg Persantine tablets because 50 mg tablets were found inside the bottles.
Wilton Brands is recalling 13,104 bottles of Yellow Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Wilton Brands is recalling 10,914 bottles of Teal Airbrush Color due to potential contamination with mold, yeast, or bacteria.
Trek Bicycle Corp. is recalling 2014 and 2015 Farley bicycles and framesets because the fork can separate from the steer tube, posing a fall hazard to the rider.
Boehringer Ingelheim is recalling 6,400 bottles of 75 mg Dipyridamole tablets because 50 mg Persantine tablets were found inside the bottles.
TEM Systems Inc is recalling ex-TEM Assay reagents for the ROTEM delta system because customers reported low or empty vials.
Wilton Brands is recalling 13,533 bottles of Pink Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 CMV IgM Assay kits due to reported increased imprecision and high coefficient of variation results.