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.
Heartland is recalling specific 2015 Big Country, Big Horn, and Landmark 365 recreational vehicles because axles may be placed too far forward, causing improper weight distribution and poor handling.
Hawkins, Inc. is recalling approximately 529 pounds of dehydrated pork stock and broth produced without the benefit of full inspection.
Ford is recalling 2014 Transit Connect vehicles because upper seat belt bolts may be improperly torqued, posing an injury risk in crashes.
All Wheel Drive Equipment Mfg. is recalling one 2011 Ford F-550 truck because a PTO pressure switch may leak oil onto the exhaust, increasing fire risk.
Sunbeam is recalling Holmes oil-filled heaters because they can spray heated oil, posing a scald hazard. No injuries have been reported.
Jaguar Land Rover is recalling 2013-2015 Range Rover and Range Rover Sport vehicles because a brake vacuum hose may be incorrectly routed, potentially causing a loss of braking assistance.
General Motors is recalling 2015 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles equipped with specific Goodyear tires that may experience tread cracking, increasing crash risk.
Toyota is recalling 2003-2004 Corolla, Corolla Matrix, Avalon, and Pontiac Vibe vehicles because electrical noise may cause air bags to deploy unexpectedly.
Chrysler is recalling specific 2002-2004 Jeep and Dodge vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.
Toyota is recalling 2011-2012 Avalon vehicles because an electrical short in the sub-woofer may cause overheating and increase the risk of fire.
Valeant Pharmaceuticals is recalling Virazole (ribavirin) inhalation solution due to positive microbial contamination found during stability testing.
Mylan Institutional, Inc. is recalling Ciprofloxacin Tablets 500 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.
Dick's Sporting Goods is recalling Fitness Gear Inversion Tables because customers reported falling and sustaining injuries. The products were distributed nationwide.
Vosges Haut-Chocolat is recalling Festival of Lights Chanukkah Gift Box Sets because the plastic menorah can catch fire if candles burn to the base.
American Roland Food Corp. is recalling Roland brand Bruschetta, Italian-Style Appetizer, because glass fragments were found in the product.
Honda is recalling 2003-2004 Odyssey and 2003 Acura MDX vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.
Maquet Medical Systems USA is recalling six units of the Tegris System because a software error switches leg movement commands for the Magnus OR table.
Chrysler is recalling 2014-2015 Jeep Cherokee vehicles because side and seat air bags may deploy unexpectedly, increasing the risk of injury or a crash.
Ford is recalling 2010-2013 Taurus and 2011-2013 Lincoln MKS vehicles because an interior door handle spring may unseat, preventing the handle from returning to its stowed position.
BD Biosciences is recalling one lot of CD8 PE reagent contaminated with CD4 FITC, which may cause incorrect patient data.
Cordis Corporation is recalling one unsterilized unit of the POWERFLEX PRO PTA Dilatation Catheter from a demonstration lot left at a hospital.
BD Biosciences is recalling two lots of Anti-Lambda APC-H7 antibody due to contamination with CD38 antibody. The product is used for in vitro flow cytometric immunophenotyping.
Mylan Institutional is recalling 3,993 cartons of Lamotrigine 200 mg tablets because they were not manufactured according to Good Manufacturing Practices.
Genetic Testing Institute is recalling specific lots of PF4 Concentrated Wash (10x) because the reagent is slightly more dilute than intended, which may cause false positive test results.
Aptalis Pharmatech Inc. is recalling approximately 49,000 Flutter Percussor respiratory devices because the packaging may be difficult to open or close.