The Recall Desk

State

Rhode Island product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50601–50625 of 76878

  • HighNHTSA·16V371000·2016-05-26

    Terex Advance Mixer Trucks Recalled for Loose Axle Hex Nuts

    Terex Advance is recalling 2015-2016 Mixer FD3000, FD4000, and FD6000B trucks because improperly tightened axle hex nuts may cause the driveshaft to disconnect, increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE MIXER FD3000, MIXER FD4000, MIXER FD6000B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V368000·2016-05-26

    Dejana Recalls Dominator Trucks Due to Potential Crane Cover Detachment

    Dejana is recalling 2013-2016 Dominator trucks because a crane valve bank cover may crack and fall off, creating a road hazard.

    Product
    DEJANA — DEJANA DOMINATOR I, DOMINATOR IV, DOMINATOR-PROPANE, DOMINATOR III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V369000·2016-05-26

    Startrans Shuttle Buses Recalled for Wheelchair Lift Platform Defects

    Supreme Corporation is recalling 2008-2014 Startrans shuttle buses because wheelchair lift platforms may crack or fall out, posing injury risks.

    Product
    STARTRANS — STARTRANS TROLLEY, AZURE HYBRID, PRESIDENT S2, PRESIDENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V362000·2016-05-26

    Kenworth Recalls 2016 W900 Trucks for Headlight Wiring Defect

    PACCAR is recalling 355 model year 2016 Kenworth W900 trucks because they may lose headlights when switching to high beams, increasing crash risk.

    Product
    KENWORTH — KENWORTH W900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16176·2016-05-26

    Box Components Recalls BMX Bicycle Forks Due to Fall Hazard

    Box Components is recalling about 4,100 carbon fiber BMX bicycle forks because the steer tube can become loose, posing a fall hazard.

    Product
    Bicycle forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16178·2016-05-26

    Osprey Recalls Child Backpack Carriers Due to Fall Hazard

    Osprey is recalling about 31,000 child backpack carriers because a cut in the plastic buckle can cause the shoulder strap to release, posing a fall hazard to the child.

    Product
    Child backpack carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V365000·2016-05-26

    Trans Tech School Bus Wheelchair Lift Recall for Platform Cracking

    Transportation Collaborative is recalling 2014-2016 Trans Tech school buses equipped with certain Ricon wheelchair lifts due to potential platform cracking or bearing displacement.

    Product
    TRANS TECH BUS — TRANS TECH BUS ST AERO, STUDENT SAFETY TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1614-2016·2016-05-25

    Monteris Medical Recalls NeuroBlate Laser Probes Due to Lens Fracture

    Monteris Medical Corp is recalling 121 NeuroBlate System SideFire Select 2.2 mm Directional Laser Probes because a sapphire lens fractured during a procedure, introducing CO2 into a patient's brain.

    Product
    NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS000-01,SFS002-01, SFS122-01, SFS222-01, SFS322-01, SFS422-01, and SFS522-01. NeuroBlate System SideFire Select Directional Laser Probes are part of the NeuroBlate System. The Monteris…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V359000·2016-05-25

    Subaru and Saab Recall Vehicles for Air Bag Inflator Rupture Risk

    Subaru is recalling specific 2003-2008 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V358000·2016-05-25

    Subaru and Saab Recall for Passenger Air Bag Inflator Rupture Risk

    Subaru is recalling specific 2003-2011 models and 2006 Saab 9-2x vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0855-2016·2016-05-25

    Renovo Patch Recalled for Lack of Approval and Subpotency

    TMIG Inc is recalling Renovo Patch because it was marketed without FDA approval and three lots were found to be subpotent.

    Product
    Renovo Patch (Capsaicin, 0.0375%, Menthol, USP 5.00%), 3-count patches per carton, Rx only, Distributed By: TMIG Inc, Marietta , GA 30062, Manufactured By: Pocono Coated Products LLC., Cherryville, NC 28021 NDC: 69176-025-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V361000·2016-05-25

    Subaru Recalls 2003-2004 Models for Air Bag Inflator Rupture Risk

    Subaru is recalling 2003-2004 Legacy, Outback, and Baja vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU OUTBACK, BAJA, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V364000·2016-05-25

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Rupture Risk

    BMW is recalling specific 2007-2011 X5 and X6 models because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    BMW — BMW X5, X6 ACTIVEHYBRID SAC, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1680-2016·2016-05-25

    Zimmer Herbert Cannulated Bone Screw Recall for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling specific lots of Herbert Cannulated Bone Screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 mm Length 47115504507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 75 mm Length 47115507507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 90 mm Length 47115509007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16174·2016-05-25

    TJX Recalls Foldable Lounge Chairs Due to Risk of Injury

    TJX is recalling about 5,200 foldable lounge chairs sold at T.J. Maxx and Marshalls because they can collapse unexpectedly, posing a fall and injury hazard.

    Product
    Foldable lounge chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1677-2016·2016-05-25

    Zimmer Manufacturing Recalls Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded, 12 mm Length 47484001200 4.0 mm Cancellous Screw Fully Threaded, 14 mm Length 47484001400 4.0 mm Cancellous Screw Fully Threaded, 16 mm Length 47484001600 4.0 mm Cancellous Screw Fully Threaded, 18 mm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1678-2016·2016-05-25

    Zimmer Manufacturing Recalls Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 70 mm Length 00225307042
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V360000·2016-05-25

    Forest River Stealth Evo Recalled for Incorrect Tire Load Range

    Forest River is recalling 2016 Stealth Evo trailers because incorrect tires may fail prematurely, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1690-2016·2016-05-25

    Becton Dickinson Recalls Shielded IV Catheters Due to Defect

    Becton Dickinson is recalling 1.3 million shielded IV catheters because a defect could cause the catheter to separate or break.

    Product
    1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog number 381700 2) 24 G x 0.56 in. BD Angiocath-N" Autoguard" shielded IV catheter (0.7 mm x 14 mm) made of FEP polymer catalog number 381720
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2016·2016-05-25

    Zimmer 3.5 mm Cortical Screws Recalled for Potential Sterility Compromise

    Zimmer Manufacturing B.V. is recalling specific lots of 3.5 mm Cortical Screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping, 10 mm Length 47483501001 3.5 mm Cortical Screw SelfTapping, 14 mm Length 47483501401 3.5 mm Cortical Screw SelfTapping, 16 mm Length 47483501601 3.5 mm Cortical Screw SelfTapping, 24 mm Length 47483502401…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V355000·2016-05-25

    Grand Design RV Recalls 2016-2017 Trailers Due to Propane Leak Risk

    Grand Design RV is recalling 2016-2017 Imagine and Reflection trailers because a propane regulator defect may cause gas leaks and fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION, IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide