State
73,827 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,054 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 708 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Oshkosh is recalling 2014-2015 S-Series concrete mixers powered by compressed natural gas because pressure relief devices may fail to vent pressure, posing a risk of tank explosion, fire, and injury.
Reyco Granning is recalling Independent Front Suspension assemblies manufactured between April 2011 and February 2015 due to loose ball joints that could separate and cause a loss of steering control.
Ford is recalling 2011-2013 and 2015 F-650 and F-750 trucks because passenger seat belt anchors may be installed in the wrong location, increasing injury risk in a crash.
Madewell is recalling about 50,600 Sightseer sandals because the metal shank can dislodge and break through the outsole, posing a fall hazard.
Arthur Schuman Inc. is recalling Bella Rosa Grated Parmesan Cheese because it may contain undeclared egg lysozyme, a potential allergen.
Mylan Institutional LLC is recalling Methotrexate Injection vials due to the presence of particulate matter.
Invacare is recalling 1,057 Pronto Air power wheelchairs because the batteries may overheat during charging, posing risks of chemical burns and property damage.
Grizzly Industrial is recalling 10-inch hybrid table saws because a loose motor pulley can strike the blade, causing metal fragments to fly and injure users.
James G. Cole, Inc. is recalling all Maxam brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.
Mylan Institutional LLC is recalling 8,340 vials of Cytarabine Injection due to the presence of particulate matter. The affected product was distributed nationwide.
Fresenius Medical Care is recalling Naturalyte Liquid Bicarbonate Concentrate due to potential bacterial contamination. The recall covers 2,264,028 units distributed nationwide.
Thor Motor Coach is recalling 2014-2015 Tuscany XTE motorhomes because the dinette table insert may flip up if sat on, posing a fall risk.
Hitachi Medical Systems America Inc is recalling 173 Oasis Coil Extension Cables used with MRI systems because they may overheat and cause burns.
Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Remel Inc is recalling 1,859 PathoDx Strep Grouping Kits because a reagent may cause weak reactions, potentially leading to failure to identify target species.
Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Trumpf Medical Systems is recalling 9,287 ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Novacare, LLC is recalling 961 bottles of Glucosamine 750 mg capsules nationwide because the product has inadequate allergen labeling.
Thor Motor Coach is recalling 290 model year 2016 Vegas and Axis recreational vehicles because the HVAC control may lock, preventing windshield defrosting and increasing crash risk.
James G. Cole, Inc. is recalling all ASN brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.
Etac Supply Center Ab is recalling 13 units of the Etac Relax wall mounted shower seat due to reports of the wall bracket cracking or breaking.
Trumpf Medical Systems is recalling 9,287 surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Trumpf Medical Systems is recalling TruLight 3000/5000 surgical lights because the front joint of the spring arm could break at the monitor interface.
Cadence Inc. is recalling 766 non-sterile Perfectum Tuberculin Glass Syringes because graduation marks are not centered with numeric position marks.
Dr. Reddy's Laboratories is recalling Rivastigmine Tartrate capsules because they failed to meet dissolution specifications.