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.

50926–50950 of 76878

  • HighNHTSA·16V276000·2016-05-10

    Elpers Truck Equipment Recalls Cranes Due to Valve Bank Cover Defect

    Elpers is recalling 35 trucks equipped with IMT cranes because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    ELPERS — ELPERS FORD F-450 W/ CRANE, INTL MAXFORCE W/ CRANE, FORD F-550 W/ CRANE, INTL 4300 W/ CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V280000·2016-05-10

    Newmar Recalls 2014-2015 Motorhomes for Power Steering Hose Failure Risk

    Newmar is recalling 93 Essex, Mountain Aire, and London Aire motorhomes because power steering hoses may fail due to high fluid temperatures, increasing crash risk.

    Product
    NEWMAR — NEWMAR ESSEX, MOUNTAIN AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16741·2016-05-10

    Honda Recalls 2016 Pioneer 1000 Off-Highway Vehicles for Door Safety Issue

    American Honda is recalling about 3,300 model year 2016 Honda Pioneer 1000 recreational off-highway vehicles because the front door can open unexpectedly, posing a risk of injury.

    Product
    Recreational off-highway vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16743·2016-05-10

    Bednest Recalls Bedside Infant Sleepers Due to Fall Hazard

    Bednest is recalling bedside infant sleepers manufactured after July 2014 because they fail to meet federal safety requirements, posing a fall hazard to babies.

    Product
    Bedside Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V275000·2016-05-09

    Spartan Recalls 2012-2015 Utilimaster Aeromaster Vehicles for Wiring Defect

    Spartan Motors is recalling 89 Utilimaster Aeromaster vehicles because a wiring defect may leave the lift gate system powered, posing an injury risk to maintenance personnel.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V273000·2016-05-06

    Dodge Journey Recall for Power Steering Hose Rupture Risk

    Chrysler is recalling 2009-2016 Dodge Journey vehicles because the power steering return hose may rupture in cold weather, causing loss of steering assist.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·027-2016 expansion·2016-05-06

    Pilgrim's Pride Recalls Chicken Products Due to Possible Foreign Matter

    Pilgrim's Pride is recalling approximately 5.2 million pounds of fully cooked chicken products that may be contaminated with extraneous metal materials.

    Product
    Pilgrim's Pride Corporation — Pilgrim's Pride Corp. Recalls Poultry Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16V274000·2016-05-06

    Land Rover Recalls Discovery Sport for License Plate Lamp Defect

    Land Rover is recalling 2015-2016 Discovery Sport vehicles because the license plate illumination lamp may fall out, making the vehicle difficult to identify at night.

    Product
    LAND ROVER — LAND ROVER DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1249-2016·2016-05-04

    Roland Fire Roasted Red Pepper Strips Recalled for Glass Fragments

    Roland Foods is recalling Fire Roasted Red Pepper Strips due to the possible presence of glass fragments in specific lots.

    Product
    Roland (R) Fire Roasted Red Pepper Strips, NET WT. 5 LB. 8 OZ. (2.5 kg), UPC 10041224456287 (carton) and 04122456280 (can), PRODUCT OF PERU -- Packed Exclusively For: ROLAND FOODS, LLC, New York, NY 10070
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1257-2016·2016-05-04

    Dietz & Watson Roasted Veggie Tortilla Wrap Recalled for Glass Fragments

    Flying Food Group LLC is recalling Dietz & Watson Roasted Veggie White Tortilla Wraps due to potential glass fragments from raw materials.

    Product
    Dietz & Watson Brand Roasted Veggie White Tortilla Wrap - 9.68 oz wrapped in plastic in a open paper box
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·16V271000·2016-05-04

    Kaufman Trailers Recalls 2015-2016 Flatbed and Wedge Car Haulers

    Kaufman is recalling 2015-2016 Flatbed Equipment and Wedge Car Hauler trailers because axle hanger lock nuts may loosen, potentially causing the axle to detach and increasing crash risk.

    Product
    KAUFMAN — KAUFMAN WEDGE CAR HAULER, FLATBED EQUIPMENT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1127-2016·2016-05-04

    Organic Traditions Sprouted Chia & Flax Seed Powder Recalled for Salmonella Risk

    Health Matters America is recalling Organic Traditions Sprouted Chia & Flax Seed Powder due to potential Salmonella contamination.

    Product
    Organic traditions SPROUTED CHIA & FLAX SEED POWDER, NET WT. 8 oz./227g (UPC barcode 854260006216), and NET WT. 16oz./454g bag (UPC barcode 85426000547) --- The product is packed in a sealed flexible plastic bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1580-2016·2016-05-04

    Hologic InPlex CF Molecular Test Recalled for False Positives and Leaking

    Hologic is recalling InPlex CF Molecular Tests due to false positive results and leaking cards, which could lead to unnecessary invasive testing during pregnancy.

    Product
    Hologic InPlex CF Molecular Test (IVD); Catalog Number: 95-432.
    Category
    Medical Device
    Distribution
    30 states
  • SevereNHTSA·16V270000·2016-05-04

    Newmar Recalls 2015-2016 Ventana Models Due to Front Sway Bar Defect

    Newmar is recalling 2015-2016 Ventana and Ventana LE vehicles because front sway bar brackets may not fit properly, risking bolt failure and loss of vehicle control.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1069-2016·2016-05-04

    WelleCo Super Elixir Greens Recalled for Potential Salmonella Contamination

    Welle Pty Ltd is recalling WelleCo Super Elixir Alkalising Greens pouches due to potential Salmonella contamination. The recall affects 150g and 300g pouches sold online in the U.S.

    Product
    The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net, 300g/10.6 oz net Fine Powder welleco.com
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-1126-2016·2016-05-04

    Health Matters America Recalls Sprouted Flax Seed Powder for Salmonella Risk

    Health Matters America is recalling Organic Traditions Sprouted Flax Seed Powder due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Organic traditions SPROUTED FLAX SEED POWDER, NET WT. 8 oz/227g, UPC 854260006261 --- The product is packed in a sealed flexible plastic bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1583-2016·2016-05-04

    Mako Surgical Recalls RESTORIS PST RIO Offset Shell Impactor

    Mako Surgical Corporation is recalling 96 units of the RESTORIS PST RIO Offset Shell Impactor due to a potential disassociation of the orientation pin.

    Product
    RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2016·2016-05-04

    Research Instruments Recalls Integra 3 Micromanipulators Due to Faulty Power Cable

    Research Instruments Ltd is recalling 380 Integra 3 micromanipulators because they were fitted with a potentially faulty power supply cable.

    Product
    Integra 3; Model Numbers: 6-54-100, 6-54-110, 6-54-150, 6-54-160 Product Usage: The Rl TDU500 Micromanipulator for Assisted Reproduction is used to accurately position microtools under a microscope for the techniques of Assisted Reproduction. The Rl Integra is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1554-2016·2016-05-04

    Horiba Recalls ABX Pentra 400 and C400 Clinical Chemistry Analyzers

    Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers due to malfunctions triggered by specific system alarms.

    Product
    Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry analyzers for clinical use. The device is intended to duplicate manual analytical procedures by performing various steps such as pipetting, mixing, heating and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1559-2016·2016-05-04

    Becton Dickinson Recalls Listeria-Contaminated Trypticase Soy Agar Plates

    Becton Dickinson is recalling Trypticase Soy Agar and MacConkey II Agar plates contaminated with Listeria monocytogenes. The non-sterile media are used for growing and detecting bacteria.

    Product
    Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Cat. Number 221291, Lot Number 6034889, Exp. Date : April 20, 2016 Product is sold in cartons of 100 plates each. Product Usage: Trypticase Soy Agar with 5% Sheep Blood is used for the growth of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1258-2016·2016-05-04

    Shaw's Eggplant and Cheese Wrap Recalled for Potential Glass Fragments

    Flying Food Group LLC is recalling Shaw's Brand Market Fresh Eggplant & Cheese Wraps due to a potential for glass fragments from a supplier raw material recall.

    Product
    Shaw's Brand Market Fresh Eggplant & Cheese Wrap, 10.0 oz packaged in plastic inside a paper open box
    Category
    Food
    Distribution
    5 states