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.
Kids II is recalling Oball Rattles because the plastic disc can break, releasing small beads that pose a choking hazard to young children.
Subaru is recalling 2017 Impreza vehicles because a software problem may cause the rearview camera display to malfunction, increasing crash risk.
Porsche is recalling 2016-2017 911 and 718 models because the passenger air bag inflator may fail to ignite, increasing injury risk in a crash.
One World Technologies is recalling Ryobi 8amp Electric Jet Fan Blowers because the internal plastic fan can break, discharging blades that pose a laceration hazard.
Goodman is recalling approximately 210,000 air handler units because the pull-out disconnects may fail to disable power, posing an electrical shock hazard to individuals servicing the equipment.
Volkswagen is recalling 2017 Beetle and Jetta GLI vehicles because incorrect tire information labels may cause operators to overload the vehicle, increasing crash risk.
Volkswagen is recalling 2017 Jetta vehicles because incorrect tire information labels may lead to vehicle overloading, increasing crash risk.
New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.
Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.
Philips Lighting is expanding a recall of about 256,000 Metal Halide Lamps because the outer bulbs can shatter, posing fire and laceration risks.
REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.
Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.
Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.
Pier 1 Imports is recalling about 363,000 glass knobs sold in the U.S. because they can break and cause lacerations.
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.
Hostess Brands is recalling Holiday White Peppermint Twinkies because an ingredient may be contaminated with Salmonella. The product was distributed nationwide.
Tosoh Smd Inc is recalling 34 units of Reporting Software for the G8 analyzer because power outages cause the software to shut down.
Sandoz Inc. is recalling Transderm Scop patches because the outer carton contains incorrect instructions for cutting the patch.
Vascular Solutions is recalling 633 units of GrebSet Micro-Introducer Kits because the guidewires have a shorter shelf life than the kit expiration date.
Cardiovascular Systems Inc is recalling 8 units of the Diamondback 360 Peripheral 1.50 Classic system because a 1.50mm Solid Crown OAD was mislabeled as a 1.50mm Crown OED.
Reckitt Benckiser LLC is recalling Durex Pleasure Pack condoms because the package labeling is missing information about the active ingredient Benzocaine.
Smith & Nephew is recalling 2,646 Dyonics Saw Blades because they are provided sterile but lack an expiration date on the label.