The Recall Desk

State

Rhode Island product recalls

73,833 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

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.

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.

57476–57500 of 76887

  • HighNHTSA·15E015000·2015-03-03

    Agility LNG Fuel System Recall for Corroded Solenoid Valves

    Agility is recalling LNG fuel systems installed on heavy-duty vehicles in 22 states and D.C. because corroded solenoid valves may cause the vehicle to stall, increasing crash risk.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15088·2015-03-03

    Dream on Me Recalls 2-in-1 Bassinet to Cradle Due to Fall Hazards

    Dream on Me is recalling 2-in-1 bassinets because wire supports can disconnect, causing fabric sides to lower and posing fall and suffocation risks.

    Product
    2-in-1 Bassinet to Cradle
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V122000·2015-03-02

    Prevost Recalls 2007-2012 Buses Due to Fuel Line Fire Risk

    Prevost is recalling 455 model year 2007-2012 buses because a missing clip allows the fuel line to rub against a coolant hose, potentially causing a leak and fire.

    Product
    PREVOST — PREVOST H3-45, H3-45 VIP, X3-45, XLII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V121000·2015-03-02

    Honda Recalls 2014-2015 Accord and CR-V for Engine Defect

    Honda is recalling specific 2014-2015 Accord and CR-V vehicles due to improperly torqued engine bolts that may cause power loss, oil leaks, or fire.

    Product
    HONDA — HONDA ACCORD, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V123000·2015-03-02

    Kia Recalls 2014-2015 Soul Vehicles Due to Accelerator Pedal Defect

    Kia is recalling 2014-2015 Soul and Soul electric vehicles because a section of the accelerator pedal may bend and fracture, potentially causing difficulty accelerating and increasing crash risk.

    Product
    KIA — KIA SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V120000·2015-03-02

    Wheeled Coach Recalls 2010 Ambulances for Electrical System Defects

    Wheeled Coach is recalling 18 model year 2010 ambulances due to potential electrical issues that may cause loss of instrument panel functions and lighting.

    Product
    WHEELED COACH — WHEELED COACH AMBULANCE-M2 CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V119000·2015-03-02

    Prevost Motorcoach Recall for Defective Fire Extinguishers

    Prevost is recalling 291 motorcoaches because certain fire extinguishers may not fully discharge, increasing injury risk during a fire.

    Product
    PREVOST — PREVOST XLII-45, X3-45, H3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·037-2015·2015-03-01

    Oscar's Hickory House Recalls Beef Jerky Due to Processing Deviation

    Oscar's Hickory House Inc. is recalling approximately 32 pounds of beef jerky due to a processing deviation that makes the product susceptible to environmental pathogens.

    Product
    Oscar's Hickory House Inc. — Oscar's Hickory House Recalls Beef Jerky Product Due To Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V113000·2015-02-27

    GM Recalls 2015 Chevrolet Cruze for Parking Brake Cable Bracket Defect

    General Motors is recalling 2015 Chevrolet Cruze vehicles because parking brake cable brackets may not be properly fastened, increasing the risk of the vehicle rolling away.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V114000·2015-02-27

    Dodge Charger and Challenger Recall for Fuel Leak Fire Risk

    Chrysler is recalling 2015 Dodge Charger and Challenger SRT vehicles because a fuel rail hose may leak, increasing the risk of a vehicle fire.

    Product
    DODGE — DODGE CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V116000·2015-02-27

    Nissan Recalls 2013-2015 Altima Vehicles for Hood Latch Defect

    Nissan is recalling 2013-2015 Altima vehicles because the secondary hood latch may fail to engage, allowing the hood to open while driving.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1035-2015·2015-02-25

    GE Healthcare MRI Systems Recalled for Potential Ferrous Object Removal Delay

    GE Healthcare is recalling MRI systems because a disconnected MRU could delay the removal of ferrous objects, posing a life-threatening injury risk.

    Product
    This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, GE 1.5T Signa HDe, Optima MR360, Brivo MR355, Signa Excite-HD 1.5T & 3T, Signa Excite 1.5T HD Twinspeed, Signa Excite 1.5T…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0392-2015·2015-02-25

    Hospira Recalls Lactated Ringer's Injection Due to Confirmed Mold Particulates

    Hospira Inc. is recalling 142,644 bags of Lactated Ringer's and 5% Dextrose Injection USP due to confirmed mold particulates in the solution.

    Product
    LACTATED RINGER'S and 5% DEXTROSE Injection USP, 1000 mL, flexible containers, Rx Only, Hospira, Inc., Lake Forest, IL 600045, NDC 0409-7929-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V111000·2015-02-25

    McNeilus Recalls Bridgemaster V Mixers Due to Parking Brake Defect

    McNeilus is recalling 2005-2014 Bridgemaster V Mixers because the optional parking brake system may fail to maintain required pressure, increasing crash risk.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1128-2015·2015-02-25

    Mako Surgical Recalls Restoris Partial Knee Application RIO Due to Burr Malfunction

    Mako Surgical Corporation is recalling 228 units of the Restoris Partial Knee Application RIO because the surgical burr may continue spinning outside the intended boundary after controls are released.

    Product
    Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System (RIO), is indicated for use in surgical knee procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0391-2015·2015-02-25

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira is recalling specific vials of 1% Lidocaine Hydrochloride Injection because a returned sample contained human hair attached to the stopper.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1126-2015·2015-02-25

    CME America Recalls BodyGuard 323 Infusion Pumps for Over-Delivery Risk

    CME America is recalling BodyGuard and BodyGuard 323 infusion pumps due to a potential for over-delivery of medication.

    Product
    BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-603XSAP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1224-2015·2015-02-25

    Probar Recalls Frosted Peanut Butter Bars for Undeclared Milk Allergen

    Probar LLC is voluntarily recalling specific lots of Frosted Peanut Butter BASE Protein Bars due to the possible presence of an undeclared milk allergen.

    Product
    PROBAR Frosted Peanut Butter BASE Protein Bar, 2.46 oz film wrapped bar packaged in 12 wrapped units per sleeve/carton. Unit UPC:8-53152-10060-5. 12 count box UPC: 8-53152-10061-2.
    Category
    Food
    Distribution
    Distributed nationwide