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.
Jayco is recalling 2014-2015 White Hawk Summit 27RBOK travel trailers because a tire may rub against the outrigger, causing premature wear or failure.
Entegra is recalling 2014-2015 Cornerstone motorhomes because incorrect seat belt attachments may cause fraying and reduced strength, increasing injury risk in crashes.
Harris Products Group is recalling about 13,000 welding torch handles in the U.S. and 350 in Canada because they can leak oxygen or fuel, posing a fire hazard.
GE Healthcare is recalling DateX-Ohmeda S/5 Single-Width Airway Modules and E-miniC accessories because a CO2 detector failure may cause incorrect low readings, potentially impairing clinical decision-making for ventilated patients.
Stryker Endoscopy is recalling 496 boxes of Disposable StrykeFlow Tips because a deformed blister pouch could compromise the product's sterility.
Utility Trailer Manufacturing Company is recalling certain 2012-2014 utility trailers because the pintle hook safety chain loop may break, increasing crash risk.
Diabetic Supply of Suncoast, Inc. is recalling Advocate Redi-Code+ blood glucose test strips because they were inappropriately labeled and marketed.
Suzuki is recalling 2010-2013 Kizashi vehicles because spider webs may block a fuel system hose, causing a fuel leak and increasing the risk of a fire.
Pentax Medical is recalling 531 ultrasound gastroscopes because aspiration needles may derail from the accessory elevator, posing a risk of patient injury.
Metagenics is recalling UltraBalance Protein Powder because it may contain undeclared soy. The recall covers specific lots distributed nationwide and internationally.
Kawasaki is recalling about 11,000 Teryx4 recreational off-highway vehicles because floor boards can allow debris to break through, posing an injury hazard.
Heartsine is recalling Pad-Pak and Pedi-Pak electrode accessories for the Samaritan PAD 300P and 350P because some sealed foil pouches are difficult to open, potentially delaying therapy.
Terumo CVS is recalling Sarns Two-stage Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Recaro is recalling specific ProRIDE and Performance RIDE child restraints because the top tether anchorage may detach in a crash, increasing injury risk.
GE Healthcare is recalling CARESCAPE Monitor B650 units because they may lose alarm sounds when an external display is connected via a USB extender with an active hub.
Honda is recalling 2015 Fit vehicles because an incorrect A-pillar cover may impair side curtain air bag performance, increasing injury risk in a crash.
GE Healthcare is recalling CARESCAPE B850, B650, and B450 patient monitors because the Patient Data Module may fail to communicate, causing partial loss of monitoring parameters.
Siemens is recalling syngo Imaging XS software due to potential miscalculation of grey scale values in specific image processing functions.
Invacare is recalling 819 M41 powered wheelchair controllers that may cause momentary loss of control due to non-standard factory programming.
Terumo CVS is recalling Sarns Malleable Dual-stage Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Alphatec Spine is recalling 14 units of the Solanas 2.1mm Fixed Depth Drill because the golden stop slid from its fixed position during use.
Terumo CVS is recalling Sarns Soft-Flow Aortic Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Terumo CVS is recalling 20 units of Sarns Soft-arc Aortic Cannulas because in-process inspections found loose fiber particulate exceeding specifications.
Siemens Healthcare Diagnostics Inc is recalling RAPIDPoint 500 Lactate Cartridges because they may display error codes for electrolyte parameters.
Terumo CVS is recalling Sarns D4 Aortic Arch Cannulae because in-process inspections found loose fiber particulate exceeding specifications.