State
73,741 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,053 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 707 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Keystone is recalling 2018-2019 Cougar recreational trailers because the wooden assembly of the outdoor propane grill may lack sufficient clearance, increasing fire risk.
Spartan is recalling 2016-2019 K2 and K3 motorhome chassis because the tag axle tire may be damaged by the DEF fill bracket, increasing crash risk.
Ferrari is recalling 2012 California, 458, and FF models because the passenger air bag inflator may explode in a crash, potentially causing serious injury or death.
Altec is recalling 2016-2017 Aerial Devices and Digger Derricks because improperly sized cable connection receptacles may cause the high voltage grounding system to fail, increasing the risk of injury.
Mobility Ventures is recalling 2015-2016 MV-1 vehicles because a failed rear turn signal does not alert the driver, increasing crash risk.
Forest River is recalling 2017-2018 Glaval transit buses because a washer in the driver's seat belt assembly may break, allowing the belt to separate from the vehicle.
Volkswagen is recalling 54,729 2018 Atlas vehicles because missing manual information can lead to seat belt buckle damage, increasing injury risk in crashes.
Shoreside Enterprises Inc. is recalling Poseidon Xtreme PLATINUM 4500 because FDA analysis found undeclared sildenafil and tadalafil, making it an unapproved drug.
The FDA is recalling 7K capsules distributed by SX Power Co. because they contain undeclared sildenafil and tadalafil, making them unapproved drugs with unestablished safety and efficacy.
Northwood is recalling 2019 Nash 24M and 29S travel trailers because tires may rub against shocks, causing damage and increasing crash risk.
Ziyad Brothers Importing is voluntarily recalling Ziyad Brand Tahini in various glass jar sizes due to potential Salmonella contamination.
Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device open or discontinuous.
Volkswagen is recalling 2018 Atlas and Tiguan vehicles because the passenger frontal air bag may tear or fail to unfold properly in a crash, increasing injury risk.
Ethicon Endo-Surgery Inc is recalling HARMONIC ACE Shears because an internal component may cause continuous or inadvertent activation of the device.
Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device open or discontinuous.
Gyrus Acmi is recalling 6,447 reusable active cords for electrosurgical generators due to a potential risk of sparking and causing a fire.
Heartware is recalling HVAD System components due to possible transient electrical connection interruptions that may cause unexpected beeping or power switching.
Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device discontinuous or open.
Arrow International Inc is recalling 416,055 ARROWg+ard Blue PLUS Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 Single-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling 4Fr. Catheter Clamps with Fastener because unsealed packaging may compromise product sterility.
Arrow International Inc. is recalling 416,055 Percutaneous Sheath Introducer Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 ARROWg+ard Blue PLUS Pressure Injectable Quad-Lumen CVC Kits because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling MAC Two-Lumen Central Venous Access Kits because unsealed packaging may compromise product sterility.
Torax Medical is recalling LINX Reflux Management System implant sutures because a manufacturing defect may cause beads to separate from wire links, potentially rendering the device discontinuous.