The Recall Desk

State

Rhode Island product recalls

73,741 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,053
Critical
221
Severe
707
Most recent
2026-10-28

Of the 3,053 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.

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38051–38075 of 76794

  • HighNHTSA·18V724000·2018-10-15

    Mercedes-Benz Recalls 2018 AMG GT Models for Air Bag Software Issue

    Mercedes-Benz is recalling 2018 AMG GT and AMG GT C Cabrio vehicles because a software error may cause both stages of the frontal air bags to deploy in a low-speed crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT, AMG GT C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V721000·2018-10-12

    Great Dane Recalls 2019 Everest Trailers for Missing Brake Rollers

    Great Dane is recalling 2019 Everest CL reefer trailers that may lack brake rollers, reducing braking effectiveness and increasing crash risk.

    Product
    GREAT DANE — GREAT DANE EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V717000·2018-10-12

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Defect

    Mazda is recalling 2010-2015 CX-7, CX-9, and Mazda6 vehicles because the front passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V718000·2018-10-12

    Riverside Dream Trailer Recall for Awning Deployment Risk

    Riverside is recalling one 2018 Dream trailer because the awning may deploy while moving, increasing crash risk. Dealers will replace the awning controller free of charge.

    Product
    RIVERSIDE — RIVERSIDE DREAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19009·2018-10-11

    Cooper Lighting Recalls Solar-Powered Outdoor LED Fixtures Due to Fire Hazard

    Cooper Lighting is recalling specific All-Pro and Defiant solar-powered outdoor LED light fixtures because the batteries can overheat and cause a fire.

    Product
    All-Pro and Defiant solar-powered outdoor LED light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V715000·2018-10-11

    Hyundai Recalls 2019 Santa Fe Vehicles Due to Air Bag Bolt Interference

    Hyundai is recalling 2019 Santa Fe vehicles because side curtain air bag mounting bolts may damage the air bags during deployment, increasing injury risk in a crash.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V710000·2018-10-11

    Toyota Recalls 2019 C-HR Vehicles Due to Rear Axle Bolt Issues

    Toyota is recalling 2019 C-HR vehicles because rear axle hub bearing bolts may be insufficiently tightened. This defect could damage brake components or cause a rear wheel to detach, increasing crash risk.

    Product
    TOYOTA — TOYOTA C-HR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V713000·2018-10-11

    BMW Recalls M3 and M4 Models for Driveshaft Connection Failure

    BMW is recalling 2016-2017 M3 and M4 vehicles because the driveshaft connection may fail, causing a loss of propulsion and increasing crash risk.

    Product
    BMW — BMW M3, M4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V712000·2018-10-11

    Erwin Hymer Recalls 2018-2019 Motorhomes Due to Generator Overcharging

    Erwin Hymer is recalling 172 motorhomes because the generator may overcharge auxiliary batteries, potentially causing acid spills if non-sealed batteries are used.

    Product
    ROADTREK — ROADTREK, HYMER, CARADO SIMPLICITY SRT, AKTIV 2.0, AKTIV, BANFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·18V711000·2018-10-11

    Toyota Recalls 2018-2019 Tundra for Incorrect Load Capacity Label

    Toyota is recalling 2018-2019 Tundra vehicles because the load carrying capacity label incorrectly overstates weight by 10 pounds, failing federal safety standards.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3321-2018·2018-10-10

    B. Braun Medical Recalls Contiplex Tuohy Sets Due to Leakage

    B. Braun Medical is recalling 1,848 Contiplex Tuohy Sets because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CONTIPLEX TUOHY SET, 18GX11/2X 1,3X40MM, Material Number 331695 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3381-2018·2018-10-10

    B. Braun Medical Recalls Catheter Connectors Due to Leakage and Disconnection

    B. Braun Medical is recalling 6,850 clamp-style catheter connectors because they may not stay closed, causing leakage or disconnection.

    Product
    CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF, Material Number 332285 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0009-2019·2018-10-10

    Endo Pharmaceuticals Recalls Robaxin-750 Due to Incorrect Dosage Labeling

    Endo Pharmaceuticals is recalling 2,856 bottles of Robaxin-750 (methocarbamol) because the labels contain incorrect dosage instructions.

    Product
    robaxin-750 (methocarbamol tablets, USP), 750 mg, 100-count bottle, Rx Only, Distributed by: Endo Pharmaceuticals Inc., Malvern, PA 19355; Manufactured by: Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274; NDC 52244-449-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0007-2019·2018-10-10

    Endologix AFX2 Bifurcated Endograft System Recall for Type III Endoleaks

    Endologix is notifying physicians about the AFX2 Bifurcated Endograft System due to observed Type III endoleaks. This is a follow-up to a December 2016 notification.

    Product
    ENDOLOGIX AFX2 Bifurcated Endograft System, Stent Graft System, Rx Only, Sterile EO, REF: BEA22-120/I20-40, BEA22-100/I20-40, BEA22-80/I20-40, BEA22-60/I20-40, BEA22-40/I20-40, BEA22-120/I16-40, BEA22-100/I16-40, BEA22-80/I16-40…
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-3364-2018·2018-10-10

    B. Braun Medical Recalls CE18TB Epidural Trays Due to Leakage

    B. Braun Medical is recalling CE18TB epidural trays because the catheter connectors may not stay closed, causing leakage or disconnection.

    Product
    CE18TB CONT EPIDURAL TRAY, Material Number 332222 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3375-2018·2018-10-10

    B. Braun Medical Recalls Epidural Catheter Connectors Due to Leakage

    B. Braun Medical is recalling 1,980 epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE17TB19C CONT EPIDURAL TRAY, Material Number 332242 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1991-2018·2018-10-10

    Neighbors LLC Recalls Gluten-Free Cookie Dough for Undeclared Almonds

    Neighbors LLC is recalling 7,264 units of Crazy About Cookies Gluten Free Chocolate Chip Cookie Dough because the packaging fails to declare almonds as an ingredient.

    Product
    Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients: Whole grain sorghum flour, cane sugar, semi sweet chocolates**Contains eggs, milk and soy.***Manufactured in the same equipment that manufactures peanut…
    Category
    Food
    Distribution
    40 states
  • SevereFDA (Devices)·Z-0008-2019·2018-10-10

    Endologix AFX Endograft Recall for Type III Endoleak Surveillance

    Endologix is notifying physicians of updated surveillance recommendations for AFX endografts due to observed Type III endoleaks.

    Product
    ENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, AFX Proximal Accessory, Infrarenal Model #/REF: A22-22/C55, A22-22/C75, A22-22/C95, A25-25/C55, A25-25/C75, A25-25/C95, A28-28/C55, A28-28/C75…
    Category
    Medical Device
    Distribution
    52 states
  • SevereNHTSA·18E095000·2018-10-10

    Alpha Technology Ignition Switch Recall Due to Engine Stall Risk

    Alpha Technology is recalling mechanical key ignition switches that may shift out of the RUN position, causing the engine to turn off and increasing crash risk.

    Product
    ELECTRICAL SYSTEM:IGNITION:SWITCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0064-2019·2018-10-10

    Leica HistoCore SPECTRA ST Slide Stainer Recalled for Electrical Safety Hazard

    Leica Microsystems is recalling 67 automated slide stainers because a single fault could expose users to hazardous mains voltage.

    Product
    Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V697000·2018-10-10

    Daimler Recalls 2018-2019 Freightliner Trucks for Engine Ground Stud Defect

    Daimler Trucks North America is recalling 2018-2019 Freightliner MT45G and MT55G vehicles because an improperly tightened engine ground stud may cause overheating and increase the risk of fire.

    Product
    FCCC — FCCC MT55G, MT45G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0006-2019·2018-10-10

    Endologix AFX Endovascular AAA System Recall for Type III Endoleaks

    Endologix is notifying physicians of surveillance recommendations for the AFX Endovascular AAA System due to observed Type III endoleaks.

    Product
    ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40, BA22-80/I20-40, BA22-60/I20-40, BA22-40/I20-40, BA22-120/I16-40, BA22-100/I16-40…
    Category
    Medical Device
    Distribution
    52 states