The Recall Desk

State

Rhode Island product recalls

73,486 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
707
Most recent
2026-10-14

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 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,047 recalls whose distribution notice names Rhode Island specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21501–21525 of 76533

  • SevereNHTSA·22V339000·2022-05-16

    2022 Freightliner Cascadia trucks recalled for disabled antilock brakes and stability control

    Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V338000·2022-05-16

    Commercial trucks recalled for incorrect gross axle weight labels

    Daimler Trucks is recalling commercial trucks with incorrect weight-rating labels that could allow unsafe overloading. Dealers will replace the labels free of charge.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4900, 4700, 5700, NEW CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V342000·2022-05-16

    Bowlus Endless Highways Travel Trailers Recalled for Gas Leak Risk

    Bowlus is recalling 2022 Endless Highways travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    BOWLUS — BOWLUS ENDLESS HIGHWAYS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V341000·2022-05-16

    Utilimaster Walk-in Van Recall for Incorrect Tire Placard Information

    Shyft Group is recalling 2022 Utilimaster Walk-in vans because tire size and pressure labels may be incorrect, potentially leading to improper tire inflation.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V333000·2022-05-13

    Ford Recalls 2021 Mustang Mach-E Vehicles for Software Defect

    Ford is recalling 2021 Mustang Mach-E all-wheel drive vehicles because a software error may cause unintended acceleration or loss of power.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V337000·2022-05-13

    Ford Recalls 2016 Super Duty Trucks for Air Bag Defect

    Ford is recalling 2016 Super Duty trucks because dust in the steering wheel clock spring may prevent the driver's air bag from deploying.

    Product
    FORD — FORD F-350 SD, F-550 SD, F-450 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V331000·2022-05-13

    2020 Ford Escape High Voltage Battery Weld Defect Recall

    Ford is recalling certain 2020 Escape and 2021 Corsair hybrid vehicles due to insufficient welds in the high voltage battery that may fail, causing loss of drive power and increased crash risk.

    Product
    FORD — FORD, LINCOLN ESCAPE, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V330000·2022-05-13

    Blue Bird Recalls 2023 Vision Transit Bus for Software Defect

    Blue Bird is recalling one 2023 Vision transit bus because incorrect software settings allow the engine to start while in gear, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E038000·2022-05-13

    Plastic Omnium Fuel Tank Assembly Recall for Engine Stall Risk

    Plastic Omnium is recalling fuel tank assemblies used in Nissan and Mitsubishi vehicles because the fuel pump may fail, potentially causing an engine stall and increasing crash risk.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V334000·2022-05-13

    2022 Ford Mustang camera misalignment disables forward collision avoidance

    Ford is recalling certain 2022 Mustang vehicles with misaligned front-facing cameras that disable forward collision avoidance and other safety features. Owners should contact Ford customer service at 1-866-436-7332 to schedule free camera realignment.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V327000·2022-05-12

    2022 Jeep Grand Cherokee Recall for Hazard Light Flashing Defect

    Chrysler is recalling 2022 Jeep Grand Cherokee vehicles because hazard lights may flash when the brake pedal is applied, potentially confusing other drivers.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V326000·2022-05-12

    2022 Jeep Wrangler Vehicles Recalled for Faulty Side Marker Lights

    Chrysler is recalling certain 2022 Jeep Wrangler vehicles with nonfunctional side marker lights. The defect may reduce vehicle visibility to other drivers, increasing the risk of a crash.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22747·2022-05-12

    Yamaha Wolverine RMAX Off-Road Vehicles Recalled for Fire and Explosion Hazards

    Yamaha is recalling about 4,130 Wolverine RMAX off-road side-by-side vehicles due to damaged fuel tanks that can leak fuel, creating fire and explosion risks. No injuries have been reported to date.

    Product
    Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0877-2022·2022-05-11

    The Mandalorian Hand Sanitizer Recalled Nationwide for Benzene Contamination

    The Mandalorian Hand Sanitizer has been recalled nationwide due to FDA-detected benzene contamination. The recall affects 346,320 bottles with lot number 20E21.

    Product
    The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-012-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0876-2022·2022-05-11

    Hand Sanitizer Product Recalled for Methanol Chemical Contamination

    Mickey Mouse Hand Sanitizer (ethyl alcohol 68%, 2.11 oz. bottles) is being recalled nationwide by Best Brands Consumer Products, Inc. due to methanol contamination in Lot #20D21 (expiration 06/30/2022).

    Product
    Mickey Mouse Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./to mL bottle, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-013-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V325000·2022-05-11

    Beta USA Recalls 2022 RR-S Motorcycles Due to Front Brake Hose Defect

    Beta USA is recalling 2022 350, 390, 430, and 500 RR-S motorcycles because an incorrect front brake hose was installed, which may disconnect and cause a loss of braking.

    Product
    BETA — BETA 350 RR-S, 390 RR-S, 430 RR-S, 500 RR-S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0944-2022·2022-05-11

    COVID-19 Rapid Test Kits Recalled for Lacking FDA Authorization

    SML Distribution is recalling 209,450 units of Skippack COVID-19 rapid test kits that were distributed without FDA authorization or clearance. The kits were distributed nationwide across Alabama, Florida, Georgia, Missouri, New York, Texas, and Wyoming.

    Product
    Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0839-2022·2022-05-11

    Losartan Potassium Tablets Recalled Due to Unacceptable Chemical Impurity Levels

    Lupin Pharmaceuticals is recalling 1.47 million bottles of Losartan Potassium Tablets due to chemical impurities exceeding acceptable limits. The affected batches were distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0849-2022·2022-05-11

    FDA Recalls Lidocaine Prilocaine Cream Due to Manufacturing Compliance Issue

    McKesson Corporation has recalled Lidocaine Prilocaine Cream 2.5%/2.5% because the manufacturer, Teligent Pharma, Inc., discontinued its stability study program, a deviation from manufacturing standards.

    Product
    Lidocaine Prilocaine Cream USP, 2.5%/2.5% Net Wt. 30 gram tube, Rx Only, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141 Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, NDC 63739-054-66
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0847-2022·2022-05-11

    Halobetasol Propionate Ointment 0.05% Recalled Due to Manufacturing Practice Deviations

    McKesson Corporation is recalling Halobetasol Propionate Ointment 0.05% nationwide after the manufacturer discontinued its stability study program, creating CGMP deviations. Over 13,200 tubes distributed in the United States, Guam, and the Northern Mariana Islands are affected.

    Product
    Halobetasol Propionate Ointment 0.05% Net Wt., 50 gram tube, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging 4071 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-998-67
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2022·2022-05-11

    Restrata Medical Device Recall: Misprinted Expiration Date on Shelf-Box Packaging

    Acera Surgical Inc is recalling 83 units of the Restrata RWM1-2X2 medical device (Lot Number 51745) due to a misprinted expiration date on the shelf-box packaging distributed nationwide.

    Product
    Restrata, Part Number RWM1-2X2
    Category
    Medical Device
    Distribution
    Distributed nationwide