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.
Spartan Motors is recalling 24 model year 2015 MM chassis because front sway bar mounting brackets may break, increasing crash risk.
Toyota is recalling 2014-2015 Prius V vehicles because the passenger air bag may not deploy in a crash due to improper calibration.
Toyota is recalling 2013-2015 RAV4 vehicles equipped with an accessory trailer light module because software may incorrectly detect a short and turn off lights, increasing crash risk.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.
Agri Star Meat & Poultry is recalling 1,690 pounds of beef franks that may contain undeclared peanuts and are misbranded as gluten-free.
Alere San Diego, Inc. is recalling INRatio PT/INR Test Strips because the system may provide INR results significantly lower than reference laboratory methods.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they have broken and produced small pieces that could be left in patients during knee replacement surgery.
DePuy Orthopaedics is recalling ATTUNE INTUITION Impactors because they may break during knee surgery, potentially leaving small fragments in the patient.
Trumpf Medical Systems is recalling JUPITER U remote controls because damaged units may cause unintended movement of operating tables during surgery.
Alere San Diego, Inc. is recalling INRatio PT/INR Monitor systems because they may provide INR results significantly lower than reference laboratory methods.
Hospira Inc. is recalling 30,840 bags of 0.9% Sodium Chloride Injection, USP, 100mL, due to a potential leak at the administrative port that compromises sterility.
Alere San Diego, Inc. is recalling INRatio 2 PT/INR monitors because they may provide results significantly lower than reference laboratory methods.
Winnebago is recalling specific 2013-2015 Minnie and Sunnybrook Remington travel trailers because the axle may crack the propane pipe fitting, creating a fire hazard.
DePuy Orthopaedics is recalling 1,130 I.M. Hole Locator Instruments because excessive force during use may lead to intra-operative femoral fracture.
Synthes (USA) Products LLC is recalling 12 Small Electric Drive units due to potential unintended starts or reverse mode failures that could cause tissue damage.
Trumpf Medical Systems is recalling IIR remote controls for JUPITER operating tables due to reports of unintended movement during surgery.
Trumpf Medical Systems is recalling JUPITER remote controls used with operating tables because complaints were reported of unintended movement during surgical cases.
Nissan is recalling 2014-2015 Pathfinder, Rogue, and Infiniti QX60 vehicles because front wheel hub fasteners may be under-torqued, risking brake separation.
Trumpf Medical Systems is recalling JUPITER remote controls for operating tables because damaged units may cause unintended movement during surgery.
Trumpf Medical Systems is recalling JUPITER cable remote controls due to reports of unintended movement during surgical cases.
Trumpf Medical Systems is recalling 137 JUPITER U cable remote controls due to reports of unintended movement during surgical cases.
Trumpf Medical Systems is recalling JUPITER remote controls due to reports of unintended movement during surgical cases caused by damaged units.
Siemens Medical Solutions is recalling 4,462 e.cam emission computed tomography systems due to a potential risk of patient finger injury.
KCI USA is recalling CelluTome Epidermal Harvesting System Harvesters because blades may drift and protrude from the top plate during shipping.
Centurion Medical Products is recalling 42 Chest Tube Tray kits because a single unit was found to contain human hair embedded in the stopper.