The Recall Desk

State

Rhode Island product recalls

73,722 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.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29701–29725 of 76775

  • ModerateFDA (Devices)·Z-2367-2020·2020-06-24

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Product Performance Verifier II

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product Performance Verifier II units because multiple coatings of AMYL Slides show imprecision on control fluids.

    Product
    VITROS Chemistry Product Performance Verifier II, Product Code 8067324, UDI # 10758750004317 - Product Usage: For in vitro diagnostic use only to quantitatively measure amylase activity in serum, plasma, and urine using VITROS 250/350/5, 1 FS/4600/XT 3400 Chemistry Systems and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1322-2020·2020-06-24

    Gaviscon Antacid Recalled for Missing Magnesium Safety Warning

    GSK is recalling Gaviscon Regular Strength Liquid Antacid bottles because the labels lack a required magnesium safety warning.

    Product
    GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowNHTSA·20V372000·2020-06-24

    Volkswagen Recalls Two 2018 Golf GTI Vehicles for VIN Label Mismatch

    Volkswagen is recalling two 2018 Golf GTI vehicles because the VIN on the Federal Certification label may not match the actual vehicle VIN, potentially preventing owners from identifying safety recalls.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1315-2020·2020-06-24

    Aurobindo Recalls Olanzapine Tablets Due to Failed Impurity Specifications

    Aurobindo Pharma USA Inc. is recalling Olanzapine Tablets, USP 7.5 mg, because the product failed impurity and degradation specifications.

    Product
    Olanzapine Tablets, USP 7.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810, NDC 66993-682-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1314-2020·2020-06-24

    Aurobindo Pharma Recalls Olanzapine Tablets Due to Impurity Failures

    Aurobindo Pharma USA Inc. is recalling Olanzapine Tablets, USP 2.5 mg, because the product failed impurities and degradation specifications.

    Product
    Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810, NDC 66993-680-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2370-2020·2020-06-24

    Abbott Vascular Recalls Xience Sierra Stents Due to Incorrect Expiration Date

    Abbott Vascular is recalling 13 units of Xience Sierra coronary stents because they bear an incorrect expiration date.

    Product
    Xience Sierra TM Everolimus Eluting Coronary Stent System, RX 3.5mm x 33mmStrength: 100 ¿g/cm¿, Nominal Everolimus Content: 209 ¿g; Lot number 903224A,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V365000·2020-06-23

    Ford Recalls 2020 Super-Duty Pickups for Transmission Defect

    Ford is recalling 2020 F-250, F-350, and F-550 Super-Duty diesel pickups because a brittle transmission part may fracture, causing engine stalls or increased braking effort.

    Product
    FORD — FORD F-250 SD, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V367000·2020-06-23

    Newell P50 Motor Coaches Recalled for Brake Pedal Obstruction Risk

    Newell is recalling 2020-2021 P50 motor coaches because a decorative cover may become lodged under the brake pedal, potentially impacting the ability to stop.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V366000·2020-06-23

    Ford Recalls 2020 Expedition and Lincoln Navigator for Headrest Weld Defect

    Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a driver's side second-row seat headrest bracket may be improperly welded, potentially failing to restrain occupants in a crash.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V364000·2020-06-22

    Mercedes-Benz Recalls 2020 Models for Turbocharger Oil Leak Fire Risk

    Mercedes-Benz is recalling 2020 C300, E350, and GLC300 vehicles because improperly tightened turbocharger oil line screws may cause leaks that increase fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 350, C 300, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V360000·2020-06-19

    Forest River Surveyor Recalled for Furnace Carbon Monoxide Risk

    Forest River is recalling 2020 Surveyor trailers because a furnace may detach from the exhaust vent, creating a carbon monoxide hazard.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V361000·2020-06-19

    2021 Forest River FR3 Leveling Jack Wiring Defect Poses Crash Risk

    The 2021 Forest River FR3 recreational vehicle has a wiring harness defect that can cause leveling jacks to deploy while driving, risking loss of vehicle control. Forest River will provide free repairs.

    Product
    FOREST RIVER — FOREST RIVER FR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V363000·2020-06-19

    2020-2021 Motorhomes Recalled for Brake Hose Chafing Risk

    Certain 2020-2021 motorhomes built on Sprinter chassis may develop a brake hose chafed by the fender liner, potentially losing brake fluid. Owners should have dealers inspect and replace brake hoses and modify fender liners at no cost.

    Product
    COACHMEN — COACHMEN, DYNAMAX, FOREST RIVER GALLERIA, ISATA, BATTISTI, SUNSEEKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V362000·2020-06-19

    Grand Design Recalls 2016-2018 Reflection Trailers for Wiring Fire Risk

    Grand Design is recalling 2016-2018 Reflection trailers because a wiring connector may allow water intrusion, potentially causing an electrical short circuit and fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20141·2020-06-18

    Lochinvar Recalls Residential Boilers Due to Carbon Monoxide Risk

    Lochinvar is recalling about 34,300 residential boilers because a flue grommet can fail, allowing carbon monoxide to escape. Consumers should contact a technician for a free repair.

    Product
    Lochinvar condensing residential boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20752·2020-06-18

    Modus Furniture Recalls Dressers Due to Tip-Over and Entrapment Hazards

    Modus Furniture is recalling Brighton, Travis, and Bevelle dressers because they are unstable without mirrors, posing tip-over and entrapment risks to children.

    Product
    Brighton, Travis and Bevelle dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2349-2020·2020-06-17

    RayStation 9A Software Recall for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation 9A software due to errors in dose calculation algorithms that could underestimate radiation therapy doses.

    Product
    RayStation 9A, UDI # 07350002010174 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2263-2020·2020-06-17

    Endologix Ovation iX Abdominal Stent Graft Systems Recalled for Polymer Leak Risk

    Endologix is recalling Ovation iX Abdominal Stent Graft Systems because a material weakness may cause polymer leaks during implantation, potentially leading to clinical events.

    Product
    Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·20138·2020-06-17

    Rexair Recalls Rainbow SRX Vacuums Due to Fire and Burn Hazards

    Rexair is recalling about 38,000 Rainbow SRX vacuums because the circuit board can spark, posing fire and burn hazards. Two fires have been reported.

    Product
    Rainbow SRX Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2348-2020·2020-06-17

    RayStation 8B Software Recall for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation 8B Service Pack 2 software due to a defect in dose calculation algorithms that could underestimate radiation dose.

    Product
    RayStation 8B Service Pack 2, UDI # 07350002010235 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
    Category
    Medical Device
    Distribution
    Distributed nationwide