The Recall Desk

State

Rhode Island product recalls

73,806 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.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40726–40750 of 76860

  • LowFDA (Drugs)·D-0617-2018·2018-03-28

    Akorn Recalls Triamcinolone Acetonide Lotion Due to Impurity Levels

    Akorn, Inc. is recalling 4,128 bottles of Triamcinolone Acetonide Lotion, USP 0.1% due to high impurity levels. The product was distributed nationwide and in Puerto Rico.

    Product
    Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V198000·2018-03-27

    Newmar Recalls Motorhomes Due to Power Steering Hose Routing Defect

    Newmar is recalling 2011-2017 Mountain Aire, Dutch Star, and Ventana motorhomes because the power steering hose may rub against the starter motor, causing fluid leaks or electrical arcing.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V191000·2018-03-26

    Western Star Trucks Recalled for Electrical Arc Fire Risk

    Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc that increases fire risk.

    Product
    WESTERN STAR — WESTERN STAR 6900, 4900, 4700, 5700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V192000·2018-03-26

    Thomas Built Buses Recall School Buses Due to Seat Bracket Crack Risk

    Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, causing seats to detach in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, MINOTOUR, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V190000·2018-03-26

    Thomas Built Buses Saf-T-Liner C2 Propane Leak Recall

    Daimler Trucks North America is recalling 2014-2019 Thomas Built Buses Saf-T-Liner C2 school buses with propane engines due to a fuel line chafing risk that could cause a leak and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V193000·2018-03-26

    Thomas Built Buses Recall Transit Models Due to Seat Bracket Defect

    Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses transit models because a wall mounting bracket may crack, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V194000·2018-03-26

    Daimler Trucks Recalls 2018-2019 Freightliner Custom Chassis XCS Vehicles

    Daimler Trucks North America is recalling 2018-2019 Freightliner Custom Chassis XCS motorhome chassis because a valve stem stabilizer may dislodge, potentially causing tire damage and increasing crash risk.

    Product
    FCCC — FCCC XCS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V188000·2018-03-23

    Ferrari Recalls 458 Italia and California Models for Air Bag Defect

    Ferrari is recalling 2009-2011 California and 2010-2011 458 Italia vehicles because passenger air bag inflators may explode during a crash, posing a risk of serious injury or death.

    Product
    FERRARI — FERRARI 458 ITALIA, CALIFORNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V197000·2018-03-23

    Lazy Daze Recalls Motorhomes with Defective Fire Extinguishers

    Lazy Daze is recalling 2012-2017 motorhomes because certain fire extinguishers may clog or detach, potentially failing to work during a fire.

    Product
    LAZY DAZE — LAZY DAZE 24' FRONT DINETTE(24FD), 27' MID-BATH (27MB), 27' REAR BATH (27RB), 27' REAR KITCHEN (27RK)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18129·2018-03-22

    SpeeCo and Woods Recall 4-Way Wedge Accessory for Log Splitters

    SpeeCo and Woods are recalling 4-way wedge accessories for hydraulic log splitters because they can detach and strike users, causing injury.

    Product
    4-way wedge accessory for hydraulic log splitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0596-2018·2018-03-21

    Pfizer Recalls Hydromorphone Hydrochloride Injection Due to Non-Sterility Concerns

    Pfizer is recalling 53,600 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass vials.

    Product
    HYDROMORPHONE HYDROCHLORIDE — HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0984-2018·2018-03-21

    Alden Optical Recalls HP49 Sphere Daily Wear Soft Contact Lenses

    Alden Optical is recalling 23 units of HP49 Sphere Daily Wear Soft contact lenses because they lack sterility assurance.

    Product
    Alden HP49 Sphere Daily Wear Soft contact; Catalog Number: AOHPS49 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V184000·2018-03-21

    MaxxD Recalls 2017-2018 A3X, A5X, and A6X Trailers for Suspension Defect

    Maxey Trailers is recalling 2017-2018 A3X, A5X, and A6X trailers because suspension arms may crack, potentially causing the axle to come loose and increasing crash risk.

    Product
    MAXXD — MAXXD A5X, A3X, A6X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0930-2018·2018-03-21

    Plant Devas Blemish Face Care Kit Recalled for Microbial Contamination

    Plant Devas Inc. is recalling Blemish Face Care Kits because FDA sampling found excessive and virulent microorganisms.

    Product
    Blemish Face Care Kit; Each kit contains: Tea Tree Gel Cleanser 1 fl oz bottle Lemon Thyme Facial Tonic HydroSoul 1 fl oz bottle Pomegranate Repair Serum 0.13 fl oz vial Green Tea Clay 0.1 oz. jar Blemish Purifying Serum 0.06 fl oz vial Light Moisture…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0931-2018·2018-03-21

    Plant Devas Ayurvedic Face Care Kit Recalled for Microbial Contamination

    Plant Devas Inc. is recalling 144 units of Ayurvedic Face Care Kits because FDA testing found excessive numbers of microorganisms.

    Product
    Ayurvedic Face Care Kit; Each kit contains: Coconut Cream Cleanser 0.5 fl oz jar Tulsi Facial Tonic HydroSoul 1 fl oz bottle Argan Intensive Facial Serum 0.13 fl oz vial Neem Immortelle Purifying Infusion 0.13 fl oz vial Lemongrass Facial Polish 0.4 oz jar…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0985-2018·2018-03-21

    Alden Optical Recalls Contact Lenses Lacking Sterility Assurance

    Alden Optical is recalling specific daily wear soft contact lenses because they lack sterility assurance. Consumers should stop using the affected lenses.

    Product
    Alden HP54 Sphere Daily Wear Soft contact; Catalog Number: AOHPS54 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0587-2018·2018-03-21

    Sagent Pharmaceuticals Recalls Methylprednisolone Sodium Succinate Injection Vials

    Sagent Pharmaceuticals is recalling 176,410 vials of methylprednisolone sodium succinate injection due to high impurity levels.

    Product
    methylPREDNISolone Sodium Succinate for Injection, USP, 125 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-808-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0597-2018·2018-03-21

    Pfizer Recalls Hydromorphone Hydrochloride Injection Vials Due to Non-Sterility

    Pfizer is recalling 29,680 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass containers.

    Product
    HYDROMORPHONE HYDROCHLORIDE — HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0981-2018·2018-03-21

    Alden Optical Recalls NovaKone Daily Wear Soft Contact Lenses

    Alden Optical is recalling NovaKone Daily Wear Soft contact lenses because they lack sterility assurance. The recall covers units distributed in the US and Canada.

    Product
    NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for daily wear for persons requiring keratoconus management for the correction of refractive ametropia (myopia, hyperopia) in aphakic and not aphakic persons…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1073-2018·2018-03-21

    Smiths Medical Recalls Misassembled Port-A-Cath Implantable Port Kits

    Smiths Medical ASD Inc. is recalling certain Port-A-Cath II kits that may contain incorrect introducer sizes or locking collars due to misassembly.

    Product
    PORT-A-CATH II PS/Titan, Tray PAC II. Labeled as: a. VEN LP, PU, 2.6MM, UL, 8.5FR/INTRO (1/EA); b. DL, LP, PU, 2.2MM, WING-LOCK, 7FR/INTRO (1/EA); c. DL, LP, PU, 3.2MM, WING-LOCK, 10FR/INTRO (1/EA)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0915-2018·2018-03-21

    Xenesta Nuvive Women's Supplement Recalled for Undeclared Milk

    Progressive Laboratories is recalling Xenesta Nuvive Women's 90-count bottles due to potential undeclared milk content.

    Product
    Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
    Category
    Food
    Distribution
    Distributed nationwide