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.
Toyota is recalling 2017 86 vehicles with automatic transmissions and ignition keys because the key may be removed without the transmission in Park, increasing the risk of the vehicle rolling away.
Bluecar is recalling 235 2016 vehicles because water may leak into the high voltage connector in heavy rain or snow, potentially causing the engine to shut down.
Toyota is recalling one 2016 4Runner and one 2017 Lexus GX460 because the front passenger air bag may not fully inflate in a crash.
Teleflex Medical is recalling 2,265 units of Weck Facial Closure Systems because the device wings may partially detach from the shield during use.
Teleflex Medical is recalling Visistat 35W disposable skin staplers because improper packaging seals mean sterility is not assured.
Prism Medical is recalling carry bars for patient lifts because a black plastic puck may break, posing a risk of harm to patients.
Encore Medical is recalling 162 Empowr PS Knee System Box Cut Guides because femoral chipping occurred during surgery.
Elekta is recalling 47 MOSAIQ Oncology Information System units because edits to particle field definition parameters may not be saved.
Stryker is voluntarily recalling 749 Performance-LOAD Ambulance Cot Fasteners because they may not fasten securely, posing a risk of injury.
Merge Healthcare is recalling Merge Cardio software versions 8.30.0 through 10.1.1 because images sent without an order may be matched to the wrong accession number.
GE Healthcare is recalling specific Avance CS2, Avance, and Amingo anesthesia devices because they may enter a System Malfunction state if a storage drawer closes with excessive force.
GF Health Products is voluntarily correcting Patriot homecare beds because contaminated motor housings may crack, potentially causing the head section to fall.
Natus Medical is recalling neoBLUE blanket LED Phototherapy Systems due to discoloration and degradation of the fiberoptic bundle at the pad and box connection.
Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because the reporting feature times out after one hour of inactivity, causing data loss.
Siemens is recalling 104 SOMATOM Definition Flash CT systems to install a software and firmware update that fixes bugs and improves performance.
C.R. Bard is recalling 452,728 units of 70cc irrigation syringes because a package defect may compromise product sterility.
Oculus Innovative Sciences is recalling professional samples of Ceramax Skin Barrier Cream because they are not meeting stability standards.
C.R. Bard is recalling 70cc Piston Syringes because a package slit defect may compromise product sterility.
Olympus Corporation of the Americas is recalling 494 HF Cable WA00014A units due to a software malfunction that may cause incorrect error codes to be generated or displayed.
Covidien LLC is recalling 5,187,100 sterile specimen containers because a packaging defect compromised the sterility of the outer surface.
C.R. Bard is recalling specific lots of 60cc Piston Syringes because a package slit defect may compromise product sterility.
Siemens Medical Solutions USA is recalling 104 SOMATOM Definition AS CT systems to install software and firmware updates that fix bugs and improve performance.
Siemens Medical Solutions is recalling 104 SOMATOM Definition Edge CT systems to install a software update that fixes bugs and improves performance.
C.R. Bard is recalling BARDIA 60cc Piston Irrigation Syringes because a slit defect in the packaging may compromise product sterility.
Becton Dickinson is recalling 4,500 BD Spinal Anesthesia Trays because a small number were incorrectly labeled as Epidural Trays.