State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Trail King is recalling 2016-2017 ACS and AACS drop deck fifth wheel trailers because the coupler plate may crack, allowing the trailer to detach from the tractor.
Siemens is recalling 35 MEVATRON KD-2 linear accelerators due to defective weld seams that could break and cause the overhead suspension to fall, posing a risk of severe injury.
Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.
Versa Marketing is recalling Fusia Asian Aspirations Szechuan Stir Fry because the product tested positive for Listeria monocytogenes. The recall affects 4,089 cases sold at Aldi stores nationwide.
Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.
Siemens is recalling 35 MEVATRON M 7400/7440 linear accelerators because a defective weld seam could break, causing the overhead suspension to fall and potentially injure patients or others.
McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.
Siemens is recalling IMMULITE Progesterone test kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Robert Rothschild Farm LLC is recalling Gift Sets with Pretzel Twists because the product is not labeled with an ingredient statement, failing to declare soy and wheat allergens.
Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because driver seats and seat belts may not secure occupants in a crash.
Parker Medical is recalling specific lots of Left Double Lumen Endobronchial Tubes because the single lung isolation feature did not function as intended.
The See Clear Company is recalling 119,829 units of color contact lenses because they may not be sterile and may have incorrect lot numbers or expiry dates.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cortitrol capsules because they contain undeclared soy, a major food allergen.
Robert Rothschild Farm LLC is recalling Gift Sets with Chocolate Pretzel Dippers because the product is not labeled with an ingredient statement, failing to declare the allergens soy and wheat.
Siemens is recalling IMMULITE 2000 Progesterone kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cholestin softgels because the product contains undeclared soy, a common allergen.
VanLeigh is recalling 2016-2017 Vilano fifth-wheel trailers because incorrect Federal Placard information may lead to vehicle overloading.
Villa Sistemi Medicali is recalling 65 Juno DRF x-ray systems because the footrest can detach from the table, causing patients to fall.
Advanced Sports International is recalling about 650 2017 Fuji bicycles because the rear wheel freehub can slip while pedaling, posing a fall hazard.
Nu Skin Enterprises is voluntarily recalling Pharmanex BioGinkgo tablets because they contain undeclared wheat, a major food allergen.
Mako Surgical Corporation is recalling 777 MAKO RIO THA Application User Guides because five AFMEA Risk Control Measures are missing from the documents.
Remel Inc is recalling Haemophilus Test Medium agar plates because poor organism growth may result in incorrect susceptibility test results.
Actavis Inc is recalling specific lots of Levofloxacin Ophthalmic Solution because the product failed impurity specifications for a related compound.
Teva Pharmaceuticals is recalling Risedronate Sodium Delayed-release Tablets because stability testing revealed low out-of-specification dissolution results.
Metrex Research is recalling CaviWipes Extra Large surface disinfectants because they may have been contaminated during the packaging process.