The Recall Desk

State

Rhode Island product recalls

73,833 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.

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56001–56025 of 76887

  • LowFDA (Drugs)·D-1079-2015·2015-05-20

    Apotex Recalls Subpotent Olanzapine Orally Disintegrating Tablets

    Apotex Inc. is voluntarily recalling specific lots of Olanzapine 5 mg orally disintegrating tablets because they contain less active drug than labeled.

    Product
    Olanzapine, Orally Disintegrating Tablets, 5 mg, a) 30-count bottle (NDC 60505-3275-03), b) 100-count blister (NDC 60505-3275-00), Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1081-2015·2015-05-20

    Apotex Recalls Subpotent Olanzapine Orally Disintegrating Tablets

    Apotex Inc. is voluntarily recalling 5,352 bottles of Olanzapine 20 mg tablets because the drug was found to be subpotent.

    Product
    Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V294000·2015-05-19

    Blue Bird All American Buses Recalled for Engine Fire Risk

    Blue Bird is recalling 2009-2016 All American non-school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V296000·2015-05-19

    NABI Transit Bus Recall for Engine Vent Tube Fire Risk

    NABI is recalling 2007-2015 LFW, BRT, and 2007-2013 CLFW transit buses because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.

    Product
    NABI — NABI LFW, CLFW, BRT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15138·2015-05-19

    Precision Trading Recalls Espresso Makers Due to Burn Risk

    Precision Trading is recalling about 4,700 PREMIUM Espresso Makers because the filler cap can crack or pop off, releasing steam and posing a burn risk.

    Product
    PREMIUM® Espresso Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15139·2015-05-19

    Kaldi's Coffee Recalls Disposable Cup Sleeves Due to Fire Hazard

    Kaldi's Coffee Roasting is recalling about 700,000 disposable paper cup sleeves because they can ignite in microwaves. Two fire incidents were reported, with no injuries.

    Product
    Disposable Cup Sleeves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V295000·2015-05-19

    Gillig Low Floor Bus Taillight Bracket Recall

    Gillig is recalling 2014-2015 Low Floor buses because taillight brackets may detach, reducing visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15E040000·2015-05-18

    Takata Frontal Driver Air Bag Inflator Module Recall

    Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E042000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for Honda, Toyota, Pontiac, Subaru

    Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V290000·2015-05-18

    RAM 4500 and 5500 Trucks Recalled for Tire Speed Rating Mismatch

    Chrysler is recalling 2014-2015 RAM 4500 and 5500 trucks because their tires are rated for a lower speed than the vehicle's maximum capability, posing a crash risk.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E041000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for 2001-2008 Vehicles

    Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V292000·2015-05-18

    New Flyer Buses Recalled for Engine Vent Tube Fire Risk

    New Flyer is recalling certain 2008-2014 buses because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V291000·2015-05-18

    Fiat 500 Electric Recall for Transmission Shifting to Neutral

    Chrysler is recalling 2013-2015 Fiat 500 electric vehicles because a software issue may cause the transmission to unexpectedly shift to neutral, increasing crash risk.

    Product
    FIAT — FIAT 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V288000·2015-05-15

    Daimler Orion VII Buses Recalled for Engine Fire Risk

    Daimler Buses North America is recalling 2007-2012 Orion VII natural gas buses because engine oil may contact hot surfaces, increasing fire risk.

    Product
    ORION — ORION VII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V287000·2015-05-15

    Nissan Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Nissan is recalling specific 2001-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the vehicle.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, FX35, I30, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E039000·2015-05-15

    Industrial Axle Company Recalls ALKO AXIS Trailer Axle Hubs

    Industrial Axle Company is recalling specific ALKO AXIS trailer axles because wheel mounting studs may fail, potentially causing wheel separation and increasing crash risk.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·079-2015·2015-05-14

    AA Poultry Recalls Chicken and Turkey Due to Unapproved Substance

    AA Poultry Processing is recalling chicken and turkey products contaminated with trichloro-s-triazinetrione, an unapproved substance.

    Product
    Pine Creek Processing LLC — AA Poultry Processing, LLC Recalls Chicken and Turkey Products Due to Use of Unapproved Substance
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0977-2015·2015-05-13

    FDA Recalls EDGE Weight Release Capsules Containing Unapproved Drugs

    Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.

    Product
    EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0991-2015·2015-05-13

    Ultra ZX Dietary Supplement Recalled for Undeclared Sibutramine and Phenolphthalein

    Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.

    Product
    ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70, Extracto de semilla de Sen 47.6, Lagrima de Coix 42, Almidon Medico 84), 30 capsule bottles, Manufactured and distributed by: Ultra ZX Labs, L.L.C. 2525 SW 3rd Ave Apt 1704 Miami, Florida 33129-2068.
    Category
    Drug
    Distribution
    Distributed nationwide