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.
Mercedes-Benz is recalling 799 model year 2017 E400 and E550 vehicles because insufficient clearance between the catalytic converter and underbody panel may cause a fire.
BMW is recalling 2011 528i, 535i, and 550i models because a replacement sensor unit may be incorrectly programmed, potentially preventing air bags and safety features from deploying in a crash.
Altec is recalling 1995-1999 Aerial Device trucks because a boom lift cylinder defect could cause uncontrolled movement, increasing injury risk.
Daimler Vans USA is recalling 2003-2006 Dodge and Freightliner Sprinter 2500 and 3500 vans because the brake warning lamp may fail to illuminate during startup, increasing crash risk.
Thor Motor Coach is recalling 528 Tuscany motorhomes because water leaks into the keyless entry module, causing electrical shorts that increase fire risk.
The Hershey Company is voluntarily recalling SoFit Protein Plus Sunflower Seeds because a supplier expanded its recall for potential Listeria monocytogenes contamination.
The Hershey Company is voluntarily recalling SoFit Protein Plus Pumpkin Seeds Sesame Garlic because a supplier expanded its recall of sunflower seeds, creating a potential Listeria monocytogenes contamination risk.
Micro Therapeutics Inc. is recalling 3,337 Alligator Retrieval Devices because the PTFE coating may delaminate and detach, potentially entering the bloodstream.
The Hershey Company is voluntarily recalling SoFit Protein Plus Almonds Jalapeno Garlic because a supplier expanded its recall of sunflower seeds, creating a potential Listeria monocytogenes contamination risk.
Micro Therapeutics Inc is recalling Pipeline Embolization Devices because PTFE coating may delaminate and enter the bloodstream.
Micro Therapeutics Inc is recalling X-Celerator Hydrophilic Exchange Guidewires because PTFE coating delamination may release material into the bloodstream.
Professional Botanicals is recalling specific lots of MealPlex and Pearl meal drinks because they contain undeclared milk, a major food allergen.
Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.
Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.
Dorman is recalling specific aftermarket clock spring assemblies because a manufacturing defect may cause the cable to tear, preventing the driver's airbag from deploying in a crash.
Truco Enterprises is recalling On the Border Cafe Style Tortilla Chips due to possible metal fragments in the corn flour.
Aluminum Trailer Company is recalling 2016-2017 Bumper Pull Toy Haulers because the fuel tank may detach, creating a fire risk.
Stryker Howmedica Osteonics is recalling specific lots of LFIT Anatomic V40 Femoral Heads because of reported taper lock failures that caused harm.
Micro Therapeutics Inc. is recalling Marathon and UltraFlow HPC Flow Directed Micro Catheters because PTFE coating may delaminate and enter the bloodstream.
Maquet Medical Systems USA is recalling Accessory Adapter part number 600525A0 because a head rest mounted to the device slipped out of the mounting rail.
Hospira is recalling Symbiq Two Channel Infusers that may display a white screen, causing the device to stop infusion and sound an alarm, which can delay or interrupt therapy.
Trumpf Medical Systems is recalling specific operating room table tops after identifying six incidents of pinched cables.
Baxter Healthcare is recalling 22,656 Revaclear MAX dialyzers because of potential particulate matter on the blood side of the device.
Hospira is recalling 10,337 Symbiq One Channel Infusers because a software issue may cause a white screen, stopping infusion and interrupting therapy.
AtriCure, Inc. is recalling 298 AtriClip LAA Exclusion Systems due to a potential component failure that could require medical intervention.