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.
Advanced Physician Solutions is recalling 77 vials of Cyanocobalamin injectable nationwide due to a lack of assurance of sterility.
CareFusion is recalling AVEA ventilators because a pressure transducer failure can stop ventilation. Nonbreathing patients may require manual ventilation or a different device.
Toyota is recalling 3,013 2015 Lexus NX200t vehicles because a damaged ABS actuator component may cause loss of vehicle stability and increase crash risk.
Advics is recalling specific antilock brake system actuators manufactured in December 2014 due to contamination that may affect valve function and vehicle stability.
Advanced Physician Solutions, Inc. is recalling Estradiol Cypionate injectable vials because the FDA determined there is a lack of assurance of sterility.
Timken is recalling aftermarket front wheel bearings with incorrect dimensions for 2001-2012 Ford Escape, 2001-2011 Mazda Tribute, and 2005-2011 Mercury Mariner vehicles due to crash risk.
Advanced Physician Solutions is recalling 416 prefilled syringes of Sodium Hyaluronate Injectable because the company cannot guarantee the product is sterile.
Strange Engineering is recalling specific Modified Street Axles because post-manufacturing heat treatment may have reduced their strength, increasing the risk of axle failure and vehicle crashes.
Advanced Physician Solutions, Inc. is recalling Glycerin (Sterile Water) 100ml 71% Injectable vials nationwide due to a lack of assurance of sterility.
Daimler Trucks is recalling 3,200 trucks and buses due to a defect that may allow engine oil to contact hot surfaces, increasing the risk of fire.
Advanced Physician Solutions is recalling Hydroxyprogesterone Caproate injectable vials because the company cannot ensure the product is sterile.
Biosense Webster is recalling 115 SMARTABLATE RF Generator Systems because two complaints reported the device inadvertently delivered RF energy during procedures.
Terumo is recalling 1,713 Advanced Perfusion System 1 bases worldwide to address power loss issues. The recall involves design changes and switch protectors.
Halyard Health is recalling specific KimVent Turbo-Cleaning Closed Suction Systems for adults because a defective internal valve may allow air to leak from the ventilator circuit.
Codman & Shurtleff, Inc. is recalling 5,463 units of the CODMAN 3000 Series Refill Set because the needles may leak from the hub connection.
Volvo is recalling 2016 XC90 vehicles because incorrect side air bag wiring may disable the safety feature, increasing injury risk in a crash.
Medtronic is recalling specific SynchroMed II implantable drug pumps because the audible alarm may stop working, potentially preventing patients from detecting issues.
Alere Scarborough, Inc. is recalling specific lots of Alere i Influenza A & B kits due to a high invalid rate and increased risk of false negative results.
Maquet Cardiovascular is recalling Quadrox-iD Adult Diffusion Membrane Oxygenators due to a potential issue that could result in blood leakage from the gas outlet port.
RaySearch Laboratories AB is recalling RayStation software versions 2.5 through 4.0 due to dose calculation issues in specific VMAT plans.
Stryker is recalling EliteCore Full Core Biopsy Devices because the cannula may extend past its intended length.
DePuy Orthopaedics is recalling 19,059 LCS COMPLETE RPS Femoral Implants because they are associated with higher revision rates and potential patello-femoral pain when the native patella is not resurfaced.
DePuy Orthopaedics is recalling LCS COMPLETE RPS knee inserts because they show higher revision rates in Australia when the patella is not resurfaced.
OptiMedica is recalling Catalys Precision Laser Systems with software version 3.00.05 because a software anomaly may provide incorrect cataract surgery parameters.
GE Healthcare is recalling D-Fend and D-Fend+ water traps because they may occlude, causing a loss of respiratory gas monitoring.