State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tommy Bahama is recalling Hula Girl Cocktail Shaker and Glass Sets because the glass shaker can break or shatter unexpectedly, posing a laceration hazard.
Kellogg USA Inc is recalling MorningStar Farms Spicy Black Bean Burgers because they contain undeclared peanut protein.
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain black particles. The recall covers 15,779,607 units distributed worldwide.
Teleflex Medical is recalling Aquapak 101 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Hayneedle is recalling about 220 fiber optic lighted Christmas trees because the motor can overheat and cause a fire. No injuries or property damage have been reported.
SCC Soft Computer is recalling specific versions of the SoftPath Laboratory Information System because diagnostic text modifications may not be saved or displayed correctly.
Jaguar Land Rover is recalling 2013-2015 Range Rovers and 2014-2015 Range Rover Sports because the occupant classification system may incorrectly disable the front passenger air bag.
Arrow International Inc is recalling 1,195 ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kits because visible foreign material was found inside the kits.
Kellogg USA Inc is recalling MorningStar Farms Chipotle Black Bean Burgers because they contain undeclared peanut protein.
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Harley-Davidson is recalling 2,476 accessory LED turn signal kits that may not flash brightly enough to meet federal safety standards, increasing crash risk.
Arthrosurface, Inc. is recalling 136 units of HemiCAP shoulder prosthetic components because they were not cleared for marketing in the US with current indications.
Stryker is recalling 399 System 6 Aseptic Housings because a failed test revealed a lack of a continual weld. Customers are instructed to return the product to Stryker.
Stryker is recalling MEDPOR Titan Max Orbital Floor and Wall implants due to incorrect barrier location and potential mix-ups with left-sided units.
TeraRecon is recalling 91 units of the Aquarius iNtuition Client Viewer due to a software anomaly in the RECIST 1.1 evaluation criteria.
Teleflex Medical is recalling specific Hudson RCI Humidifier Adaptors because the packages may contain black particles. The recall affects units distributed worldwide.
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
HVL, LLC is recalling 278 bottles of Melatonin Control-Released Tablets that contained a vegetarian digestive enzyme instead of melatonin.
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain foreign material, specifically black particles.
Natus Medical is recalling EPWorks software versions prior to 6.0 used in the Xltek Protektor Stimulator. A software error prevents remote users from stopping free run waveform groups.
Arthrosurface, Inc. is recalling 138 Taper Post Fixation Components because they were not cleared for marketing in the US with current indications.
Arthrosurface, Inc. is recalling 182 units of Athrosurface Taper Post Fixation Components because they were not cleared for marketing in the US with current indications.
Sun Pharma Global Fze is recalling 3,263 bottles of Levetiracetam extended release tablets because they failed to meet dissolution specifications at the 6-month time point.
Teleflex Medical is recalling 2,640 units of LMA Supreme (New Cuff) Size 5 devices because some may be mislabeled as Size 5 but are actually Size 4.