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.

30326–30350 of 76775

  • ModerateFDA (Devices)·Z-1820-2020·2020-05-06

    Smiths Medical Recalls Mislabeled Portex Lumbar Puncture Trays

    Smiths Medical ASD Inc. is recalling 100 units of Portex Lumbar Puncture Trays because the inner trays were mislabeled with an incorrect model number.

    Product
    Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide all the materials necessary to measure cerebrospinal fluid pressure and/or collect cerebrospinal fluid specimens. Key components include skin prep materials…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1797-2020·2020-05-06

    Siemens Atellica CH 930 Analyzer Recall for Software Defect

    Siemens is recalling Atellica CH 930 Analyzers with specific software versions due to a defect that may cause incorrect test results.

    Product
    Atellica CH 930 Analyzer, Siemens Material Number 11067000 with software version v1.21.0 SP1 or lower
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1800-2020·2020-05-06

    Bio-Rad Autoimmune EIA Anti-Tissue Transglutaminase IgA Test Recalled for Lot Bias

    Bio-Rad Labs is recalling 376 units of the Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test, Lot 18200A, due to elevated lot-to-lot bias affecting antibody measurements.

    Product
    Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product Usage: The assay is an aid in the diagnosis of celiac disease (gluten-sensitive enteropathy) and should be used in conjunction with other serological tests and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1805-2020·2020-05-06

    Obalon Balloon System Recalled Due to Touchscreen Calibration Issues

    Obalon Therapeutics is recalling 45 Obalon Balloon Systems because the touchscreen may lose calibration, preventing balloon inflation.

    Product
    Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen; Software version 02.00.00.0076 - Product Usage: The System is intended to be used as an adjunct to a moderate intensity diet and behavior modification program. All balloons must be removed 6 months after the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1798-2020·2020-05-06

    Boston Scientific Recalls MoXy Laser Fiber for Breakage Risk

    Boston Scientific is recalling MoXy Laser Fibers to update instructions and reduce the likelihood of metal cap and fiber tip breakage.

    Product
    MoXy Laser Fiber, Material Number 0010-2400 - Product Usage: The fiber can be used for the surgical incision/excision, vaporization, ablation, hemostasis and coagulation of soft tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1834-2020·2020-05-06

    Ortho VITROS TT4 Reagent Pack Recalled for Calibration Failures

    Ortho Clinical Diagnostics is recalling VITROS TT4 Reagent Packs due to increased unsuccessful calibrations. The recall affects 3,181 units distributed in the US and 23 other countries.

    Product
    VITROS Immunodiagnostic Products TT4 Reagent Pack, Product Code 8744468
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1256-2020·2020-05-06

    Dr. Reddy's Recalls Esomeprazole Magnesium Capsules Due to Discoloration

    Dr. Reddy's Laboratories is recalling 1,752 bottles of Esomeprazole Magnesium 40 mg capsules because the product contains brown pellets.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V251000·2020-05-05

    Freightliner M2 Trucks Recalled for Potential Loss of Drive Power

    Daimler Trucks is recalling 2019 Freightliner Business Class M2 trucks because a wire harness connector may unplug, causing sudden loss of drive power and power steering.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V249000·2020-05-05

    Blue Bird Recalls Vision Buses Due to Fuel Line Chafing Risk

    Blue Bird is recalling 2018-2021 Vision buses with Ford 6.8L engines because parking brake cables may chafe fuel lines, creating a fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V252000·2020-05-05

    Thomas Built Buses Recalls Saf-T-Liner HDX for Small Emergency Exit Labels

    Daimler Trucks North America is recalling 2010-2020 Thomas Built Buses Saf-T-Liner HDX school buses because the rear emergency exit window labels may have lettering that is too small to read easily.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V248000·2020-05-04

    Hyundai Recalls 2016 Genesis Coupe Due to Air Bag Mounting Bolt Issue

    Hyundai is recalling 2016 Genesis Coupe vehicles because driver-side air bag mounting bolts may be insufficiently tightened, posing an injury risk in a crash.

    Product
    HYUNDAI — HYUNDAI GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E027000·2020-05-03

    Harbor Freight Recalls Pittsburgh Automotive 3 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling Pittsburgh Automotive 3 Ton Heavy Duty Steel Jack Stands because the ratchet teeth may not engage properly, causing the stand to fail under load.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05022020·2020-05-02

    Chicken Noodle Soup Recalled for Undeclared Egg Allergen

    USDA issued a public health alert for Roundy's chicken noodle soup containing undeclared egg. No illnesses have been reported.

    Product
    Roundy's Supermarkets, Inc. — FSIS Issues Public Health Alert for Chicken Noodle Soup Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V246000·2020-05-01

    Mercedes-Benz Recalls 2020 GLB 250 for Water Intrusion Electrical Risk

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because water entering the foot wells may damage electrical components, causing the instrument cluster to go blank or the engine to stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V245000·2020-05-01

    Aprilia Motorcycles Recalled for Front Brake Pad Corrosion Risk

    Piaggio is recalling 3,287 Aprilia motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.

    Product
    APRILIA — APRILIA TUONO RF, RSV4 RR, RSV4 RF, TUONO RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20116·2020-05-01

    Epson Recalls Scanner Power Adapters Due to Fire and Burn Hazards

    Epson is recalling power adapters sold with V-series scanners because they can overheat, melt, and catch fire. Consumers should stop using them and contact Epson for a free replacement.

    Product
    Power adapters sold with Epson scanners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V247000·2020-05-01

    Mercedes-Benz Recalls G-Class Vehicles Due to Child Safety Lock Label Error

    Mercedes-Benz is recalling 2019-2020 G550 and G63 vehicles because the child safety lock symbol may indicate the incorrect status, posing a risk to unrestrained children.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20740·2020-04-30

    Essential Trading Post Recalls Wintergreen and Birch Oils for Packaging Defect

    Essential Trading Post is recalling Wintergreen and Birch Essential Oils because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Essential Trading Post Wintergreen and Birch Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20114·2020-04-30

    Bellman & Symfon Recalls Flash Receivers for Hearing-Impaired Users

    Bellman & Symfon is recalling Flash Receivers because the backup battery may fail to charge, preventing the unit from alerting hearing-impaired users to emergencies.

    Product
    Flash Receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1746-2020·2020-04-29

    Wilson-Cook Recalls HEMO-10 Hemospray Endoscopic Hemostat Devices

    Wilson-Cook Medical is recalling HEMO-10 Hemospray Endoscopic Hemostat devices because the handle or activation knob may crack or break, potentially causing the carbon dioxide cartridge to exit the handle.

    Product
    HEMO-10 Hemospray Endoscopic Hemostat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1786-2020·2020-04-29

    Degania Recalls Temperature Sensing Foley Catheters Due to Inspection Failures

    Degania Medical Devices is recalling specific lots of temperature sensing Foley catheters because inadequate incoming inspection practices were used on the thermistor sensors.

    Product
    Temperature Sensing 100% Silicone Foley Catheter, Part Number 102202101863DO - Product Usage: is a 3 lumen silicone catheter with a sensor to measure temperature while draining the urinary bladder.
    Category
    Medical Device
    Distribution
    Distributed nationwide