The Recall Desk

State

Rhode Island product recalls

73,187 recalls have nationwide distribution and so reach Rhode Island. 3,047 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,047
Critical
221
Severe
572
Most recent
2026-09-30

Of the 3,047 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 572 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,047 recalls whose distribution notice names Rhode Island specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13476–13500 of 76234

  • ModerateFDA (Devices)·Z-0630-2024·2024-01-10

    KeySplint Hard Clear dental devices recalled for incorrect instructions

    Keystone Industries is recalling 336 units of KeySplint Hard Clear due to incorrect Instructions for Use packaged with the product. Affected units received KeySplint Soft instructions instead.

    Product
    KeySplint Hard Clear - Indicated for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints, repositioners, and retainers Item No.: 4220011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0626-2024·2024-01-10

    Patella implant component recalled due to labeling error

    Encore Medical has voluntarily recalled a patella implant component (REF 130-03-738) due to mislabeling. The recall involves 2 units distributed nationwide.

    Product
    REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V008000·2024-01-09

    PL Custom Recalls 2020-2024 Ambulances Due to Electrical Fire Risk

    PL Custom is recalling 2020-2024 Type 1 and Type 3 ambulances because a firmware defect may cause electrical circuits to overheat and catch fire.

    Product
    PL CUSTOM — PL CUSTOM TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V009000·2024-01-09

    Alexis Fire Equipment Recalls 2022-2023 Fire Trucks Due to Electrical Fire Risk

    Alexis Fire Equipment is recalling 56 fire trucks from 2022-2023 because a firmware defect may prevent electrical circuits from shutting off, increasing fire risk.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V006000·2024-01-08

    E-One Recalls Fire Trucks Due to Electrical Fire Risk

    E-One is recalling 408 fire trucks because a wiring defect may cause electrical circuits to overheat and start a fire.

    Product
    E-ONE — E-ONE TYPHOON N, COMMERCIAL, CYCLONE E, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V007000·2024-01-08

    Marion Body Works Recalls 2024 Spartan Fire MetroStar Vehicles for Brake Defect

    Marion Body Works is recalling 2024 Spartan Fire MetroStar vehicles because a defective inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    MARION BODY WORKS — MARION BODY WORKS SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V005000·2024-01-08

    Coachmen Galleria motorhomes recalled for damaged wiring causing power steering loss

    Forest River is recalling Coachmen Galleria motorhomes (2020–2024) because battery boost wiring may become damaged, causing an electrical short circuit that results in loss of power steering, increasing crash risk.

    Product
    COACHMEN — COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V003000·2024-01-05

    Forest River Recalls 2020 Cherokee Travel Trailers Due to Draw Bar Defect

    Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2024·2024-01-05

    Salm Partners Recalls Turkey Kielbasa Due to Bone Fragments

    Salm Partners, LLC is recalling ready-to-eat turkey kielbasa products due to possible contamination with bone fragments.

    Product
    Salm Partners, LLC — Salm Partners, LLC Recalls Ready-to-Eat Turkey Kielbasa Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V004000·2024-01-05

    Mickey Truck Bodies Recalls 37 Vehicles Due to Electrical Arcing Risk

    Mickey Truck Bodies is recalling 37 commercial trucks from 2020-2023 because exposed wiring on the refrigeration unit may cause electrical arcing and increase fire risk.

    Product
    MICKEY TRUCK BODIES — MICKEY TRUCK BODIES ISUZU NQR, CHEVROLET 5500 HD, HINO L6, CHEVROLET LCF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V002000·2024-01-04

    Terex Advance Concrete Mixer Trucks Recalled for Drum Separation Risk

    Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.

    Product
    TEREX ADVANCE — TEREX ADVANCE CHARGER, COMMANDER, MM300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24075·2024-01-04

    Ride Aventon Sinch.2 Folding E-Bicycles Recalled for Unexpected Acceleration

    Ride Aventon is recalling about 2,300 Class 2 Sinch.2 folding e-bicycles because they can accelerate unexpectedly, causing loss of control and crash hazards. The firm has received six reports of unexpected acceleration but no injuries.

    Product
    Class 2 Sinch.2 Folding E-Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24074·2024-01-04

    Bell Slope Adult Bicycle Helmets Recalled for Head-Injury Risk

    Bell Sports is recalling about 2,360 Bell Slope Adult Helmets because the strap anchor can dislodge during impact, violating safety standards and risking head injury in a crash.

    Product
    Bell Slope Adult Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24077·2024-01-04

    UBBCARE Play Yard Mattresses Recalled for Suffocation Hazard

    UBBCARE play yard mattresses violate federal safety standards for crib mattresses and pose a suffocation hazard to infants. The mattresses are missing required warnings and labels and fail thickness tests. No injuries have been reported.

    Product
    UBBCARE Play Yard Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24076·2024-01-04

    Homedics Therapist Select Percussion Massagers Recalled for Fire and Burn Hazards

    Homedics is recalling about 46,000 Therapist Select Percussion Personal Massagers (model HHP-715) because they can overheat while charging, creating fire and burn risks. The company has received 17 overheating reports, including one burn injury.

    Product
    Therapist Select Percussion Personal Massagers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowCPSC·24072·2024-01-04

    H.H. Brown Redeemer Work Boots Recalled for Non-Puncture-Resistant Sole

    H.H. Brown Shoe Company is recalling about 2,360 Redeemer DH 5379 work boots sold from February 2023 through October 2023 because the sole is not puncture-resistant, posing an injury hazard. No injuries have been reported.

    Product
    Redeemer Men's Work Boot Model DH 5379
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0599-2024·2024-01-03

    Megadyne MEGA SOFT Return Electrode Recalled for Serious Burn Injuries

    Megadyne Medical Products is recalling approximately 2,312 MEGA SOFT Universal Plus Patient Return Electrodes due to reports of serious patient burn injuries, including third-degree burns. The product is now restricted to patients age 12 and older.

    Product
    Product Code 0847, MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Plus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2024·2024-01-03

    Busseto Foods Recalls Charcuterie Meat Due to Salmonella Risk

    Fratelli Beretta USA is recalling Busseto Foods charcuterie samplers due to possible Salmonella contamination linked to a multistate outbreak investigation.

    Product
    Fratelli Beretta USA, Inc. — Fratelli Beretta USA, Inc. Recalls Busseto Foods Brand Ready-to-Eat Charcuterie Meat Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0600-2024·2024-01-03

    Megadyne Patient Return Electrode Recalled Due to Serious Burn Injury Reports

    Megadyne Medical Products is recalling the MEGA SOFT Universal Plus Patient Return Electrode due to reports of serious burn injuries, including third-degree burns. The device should not be used in patients under 12 years old.

    Product
    Product Code 0848, MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Plus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0597-2024·2024-01-03

    MEGADYNE MEGA SOFT Return Electrode Recalled Due to Reported Patient Burn Injuries

    Megadyne Medical Products is recalling its MEGA SOFT Universal Patient Return Electrode due to reports of patient burn injuries, including third-degree burns requiring intervention. The product is now limited to use in patients age 12 and older.

    Product
    Product Code 0845, MEGADYNE MEGA SOFT Universal Patient Return Electrode, Reusable Patient Return Electrode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0208-2024·2024-01-03

    Sure Unscented Deodorant Aerosol Recalled for Benzene Contamination

    Sure Unscented Deodorant Aerosol is being recalled nationwide due to benzene contamination. Consumers should stop using affected cans and contact the manufacturer.

    Product
    Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0209-2024·2024-01-03

    Sure Regular Antiperspirant Deodorant Aerosol Recalled for Benzene Contamination

    Sure Regular Antiperspirant Deodorant Aerosol (6 oz cans) sold nationwide in the US and Canada is being recalled due to benzene contamination. All lots expiring on or before August 2023 are affected.

    Product
    Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0561-2024·2024-01-03

    Medline Tracheostomy Care Kits Recalled for Sharp Brush and Bristle Detachment

    Medline is recalling 620,735 tracheostomy care kits because the brush component has a sharp edge that can puncture tubing and injure users, and bristles can detach during use.

    Product
    Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray with 14 Fr Suction Catheter, REF DYND40580, Sterile; (2) Medline Tracheostomy Clean and Care Tray, REF DYND4061030, Sterile; (3) Medline Basic Tracheostomy Care Kit, REF CC3T4691A, Sterile; (4)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0562-2024·2024-01-03

    Medline Nursing Skills Kit: Tracheostomy Brush Sharp Edge and Bristle Defect

    Medline is recalling 172 Nursing Skills kits due to defects in the tracheostomy brush component. The brush has a sharp edge that can puncture tubing and cause user injury, and bristles may detach during use.

    Product
    (1) Nursing Skills kit, SKU #EDUC05038B, Case UPC 40195327019878, Non-sterile, For Training Purposes Only, Not For Human Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide