State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blue Bird is recalling 2020 Vision and All American school buses because the roof hatch handle may break, preventing emergency exit.
KME is recalling various 2016-2020 Predator and Predator Panther fire trucks because hydraulic velocity fuses may fail to lock the cab during a system failure, posing an injury risk to occupants.
Lidl is recalling Playtive Junior Wooden Grasping Toys because the wheels can detach, posing a choking hazard to young children.
Levolor is recalling about 30,000 custom cellular shades because the pull cords are joined by a non-breakaway connector, posing a strangulation hazard to small children.
Lifetime Brands is recalling Fitz and Floyd Nevaeh White can mugs because they can crack or break when exposed to hot liquids, posing burn and laceration hazards.
Micro Bird is recalling 52 model-year 2019 MB II propane-powered buses because a melted grounding wire could cause an engine compartment fire.
Maserati is recalling 2019 Levante vehicles because misadjusted LED headlights may impair visibility for other drivers, increasing crash risk.
PharMEDium Services is recalling 28,140 hydromorphone syringes because the product is labeled as sulfite-free but contains sulfites.
Siemens is recalling eight Artis fluoroscopic X-ray systems because screws on the ceiling-mounted support may loosen or snap, posing a risk of severe injury.
Siemens is recalling 63 Artis zee X-ray systems because ceiling support screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 29 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.
Keystone is recalling 2020 Crossroads Hampton and Sunset trailers because an incorrectly wired breakaway switch may prevent brakes from functioning if the trailer separates from the tow vehicle.
Siemens is recalling 120 Artis X-Ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 12 Artis X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 11 Artis X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 276 Artis zee ceiling-mounted X-ray systems because screws joining the pivot bearing to the ceiling support may work loose or snap off, posing a risk of severe injury.
Siemens is recalling two Artis Q zeego X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 131 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling eight Artis X-ray systems because screws on the ceiling-mounted support may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 73 Artis X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury.
Baxter Healthcare is recalling Revaclear 300 dialyzers because ruptured fibers may cause blood leaks during hemodialysis treatment.
Siemens is recalling 15 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.
Custom Molded Products is recalling about 16,000 diverter valve caps sold with certain Master Spas hot tubs and swim spas because the caps can pop off and strike bystanders.
Ortho-Clinical Diagnostics is recalling 2,411 refurbished VITROS 250 Chemistry Systems due to potential negative drift in Creatine Kinase (CK) test results.
Baxter Healthcare is recalling Revaclear 400 dialyzers because ruptured fibers may cause blood leaks during hemodialysis treatment.