State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ziemer USA Inc. is recalling 26 Femto LDV Z-Generation femtosecond surgical lasers because they were not shipped with the required Starter Kits.
NatureBox, Inc. is recalling Sweet Blueberry Almonds because the product label failed to list soy lecithin, an ingredient included in the recipe.
Ortho-Clinical Diagnostics is recalling VITROS 3600 systems because software versions 3.1 and below may fail to identify expired calibrations.
Stryker is recalling 3,625 SurgiCounter Charging Cradles because they may fail to charge the scanner or download data after surgical procedures.
Porsche is recalling 2011-2012 Cayenne S Hybrid and 2012 Panamera S Hybrid vehicles because the fuel injection system may leak, increasing fire risk.
Polar Tank Trailer is recalling 2015 ATB6, APX0, and SRJH trailers due to a parking brake actuator defect that may cause brake drag and fire.
Polaris is recalling 2015 Slingshot and Slingshot SL motorcycles because roll hoops may not meet hardness specifications, increasing injury risk in rollovers.
Jayco is recalling 2015 Eagle 30.5 BHLT fifth wheel trailers because the tire labels list incorrect tire sizes. Owners should contact Jayco to receive corrected labels to prevent potential tire failure.
Volkswagen is recalling 26,008 Audi and Volkswagen vehicles because a fuel leak in the injection system could cause a fire.
Frontline Communications is recalling 2007-2011 Mobile Medical Units because wheelchair lift platform side plates may crack, posing an injury risk.
Tucker Rocky is recalling specific Speed and Strength SS500DVD motorcycle helmets because they fail to meet federal safety standards, increasing the risk of serious injury in a crash.
La Guadalupana Wholesale is recalling chicken tamales produced without required HACCP and Listeria programs. No illnesses have been reported.
Sentry Food Solutions is recalling approximately 14,130 pounds of chicken and beef products because they may contain undeclared peanuts.
Kalle USA is recalling approximately 168,473 pounds of dehydrated pork products that were not presented for U.S. inspection. No adverse reactions have been reported.
La Guadalupana Wholesale is recalling 8,856 pounds of chicken tamales because they were produced without a required HACCP plan or Listeria program.
Kia is recalling 86,880 model year 2014 Forte vehicles because the cooling fan resistor may overheat and melt, increasing the risk of a vehicle fire.
Spartan Motors is recalling 24 model year 2015 MM chassis because front sway bar mounting brackets may break, increasing crash risk.
Toyota is recalling 2014-2015 Prius V vehicles because the passenger air bag may not deploy in a crash due to improper calibration.
Toyota is recalling 2013-2015 RAV4 vehicles equipped with an accessory trailer light module because software may incorrectly detect a short and turn off lights, increasing crash risk.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.
Agri Star Meat & Poultry is recalling 1,690 pounds of beef franks that may contain undeclared peanuts and are misbranded as gluten-free.
Alere San Diego, Inc. is recalling INRatio PT/INR Test Strips because the system may provide INR results significantly lower than reference laboratory methods.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they may break during knee surgery, potentially leaving small fragments in the patient.
Alere San Diego, Inc. is recalling INRatio PT/INR Monitor systems because they may provide INR results significantly lower than reference laboratory methods.