The Recall Desk

State

Rhode Island product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35401–35425 of 76791

  • LowFDA (Devices)·Z-1221-2019·2019-05-01

    Maquet Edi Catheter Recalled for Incorrect Expiry Date Labeling

    Getinge is recalling Maquet Edi Catheters because the single-pack boxes are labeled with the wrong expiry date. The recall covers 17 boxes distributed in the US and several countries.

    Product
    Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg Product Code/REF Number: 6685775 Product Usage: The Edi Catheter is a single-use naso-gastric feeding tube with an electrode array of ten electrodes. The Edi Catheter is intended for: - Detecting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1241-2019·2019-05-01

    Akorn Recalls Fentanyl Citrate Injection Due to Impurity Specification Failure

    Akorn Inc. is recalling Fentanyl Citrate Injection, USP, 100 mcg/2 mL, because it failed impurity specifications during stability testing.

    Product
    Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1242-2019·2019-05-01

    Zydus Recalls Carvedilol Tablets Due to Foreign Tablet Fragments

    Zydus Pharmaceuticals is recalling Carvedilol tablets 3.125 mg because a customer complaint identified a fragmented tablet of another drug product mixed in the bottle.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V337000·2019-04-30

    Smeal Recalls 2017-2019 Aerial Fire Apparatus Due to Missing Welds

    Smeal is recalling 2017-2019 Aerial Fire Apparatus vehicles because missing joint welds in the base rail may cause the aerial device to collapse.

    Product
    SMEAL — SMEAL AERIAL FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V338000·2019-04-30

    Spartan Gladiator Aerial Vehicles Recalled for Frame Cracks

    Spartan Motors is recalling 2004-2016 Gladiator aerial vehicles because cracks in the tiller frame may cause the device to fall, risking injury.

    Product
    SPARTAN — SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E032000·2019-04-30

    Strategic Sports Recalls Zox Sierra ST-560 Motorcycle Helmets

    Strategic Sports is recalling Zox Sierra ST-560 helmets because they may not adequately protect the wearer in a crash. Owners should return the helmet for a full refund.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V331000·2019-04-30

    Southeast Apparatus Recalls 2017-2018 Fire Trucks Due to Brake Light Defect

    Southeast Apparatus is recalling 39 fire trucks from 2017-2018 because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    SOUTHEAST APPARATUS — SOUTHEAST APPARATUS RESCUE TRUCK, TANKER, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V334000·2019-04-29

    Airstream Recalls 2018-2020 Travel Trailers Due to Spare Tire Carrier Defect

    Airstream is recalling 2018-2020 travel trailers because the spare tire carrier may contact the ground, causing the tire to detach and create a road hazard.

    Product
    AIRSTREAM — AIRSTREAM NEST, SPORT, CLASSIC, TOMMY BAHAMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V333000·2019-04-29

    New England Wheels Recalls Modified Ford Transit and Ram Promaster Vehicles

    New England Wheels is recalling 2014-2018 Ford Transit and 2014-2019 Ram Promaster vans modified with Freedman Go-ES Foldaway seats because the seat cushions may not stay locked in place during a crash.

    Product
    FORD — FORD, RAM TRANSIT, PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·19112·2019-04-26

    Kids II Recalls All Rocking Sleepers Due to Infant Death Reports

    Kids II is recalling all Rocking Sleepers because five infant deaths have occurred. Consumers should stop using the product and contact the company for a refund.

    Product
    All models of Kids II Rocking Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V330000·2019-04-26

    Mitsubishi Recalls 2017-2018 Mirage G4 for Air Bag Software Defect

    Mitsubishi is recalling 26,016 2017-2018 Mirage G4 vehicles because a software error may disable air bags. Dealers will reprogram the system free of charge.

    Product
    MITSUBISHI — MITSUBISHI MIRAGE G4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V324000·2019-04-25

    Ram 1500 Recall: Rear Driveshaft Weld Defect May Cause Fracture

    FCA US is recalling 2018-2019 Ram 1500 trucks because an incomplete weld on the rear driveshaft may crack or fracture, creating a road hazard or loss of drive power.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V328000·2019-04-25

    GM Recalls 2017-2019 Chevrolet and GMC Trucks for Fire Risk

    General Motors is recalling specific 2017-2019 Chevrolet Silverado and GMC Sierra trucks because a short circuit in the engine block heater could cause a fire.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 4500, SILVERADO 2500, SILVERADO 3500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V327000·2019-04-25

    Volvo Recalls 2019 S60 Vehicles for Rear Suspension Lock Nut Issue

    Volvo is recalling 2019 S60 vehicles because rear suspension lock nuts may not be properly tightened, which could cause sudden handling changes and increase crash risk.

    Product
    VOLVO — VOLVO S60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19111·2019-04-25

    Viessmann Recalls Vitodens Boilers Due to Carbon Monoxide Hazard

    Viessmann is recalling Vitodens 200-W and 222-F boilers because a corroded heat exchanger can leak flue gases, posing a carbon monoxide poisoning hazard.

    Product
    Vitodens boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V326000·2019-04-25

    Jaguar Recalls 2014-2015 F-TYPE Vehicles for Air Bag Sensor Wiring Issue

    Jaguar is recalling 2014-2015 F-TYPE vehicles because a seatbelt sensor wiring error may cause the front passenger air bag to deploy incorrectly, increasing injury risk for children.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19742·2019-04-25

    TriDerma Recalls Pain Relief Cream for Child-Resistant Packaging Failure

    TriDerma is recalling Pain Relief Cream with Lidocaine because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.

    Product
    Pain Relief Cream with Lidocaine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1206-2019·2019-04-24

    Herbal Coffee Recalled for Undeclared Erectile Dysfunction Drugs

    The FDA is recalling Kopi Jantan Tradisional Natural Herbs Coffee because it contains undeclared sildenafil and tadalafil, unapproved drugs for erectile dysfunction.

    Product
    Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah, Malaysia, UPC 9 557205 060083.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1184-2019·2019-04-24

    Serum Tears 50% Ophthalmic Drops Recalled for Sterility Assurance Issues

    Anderson Compounding Pharmacy is recalling Serum Tears 50% Ophthalmic Drops due to a lack of sterility assurance. All lots are affected nationwide.

    Product
    Serum Tears 50% Ophthalmic Drops, 1 mL Dropper, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
    Category
    Drug
    Distribution
    Distributed nationwide