The Recall Desk

State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47601–47625 of 76871

  • SevereNHTSA·16V832000·2016-11-17

    BMW Recalls 2011 5-Series Vehicles for Air Bag Sensor Defect

    BMW is recalling 2011 528i, 535i, and 550i models because a replacement sensor unit may be incorrectly programmed, potentially preventing air bags and safety features from deploying in a crash.

    Product
    BMW — BMW 535I, 550I, 528I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V834000·2016-11-17

    Thor Motor Coach Recalls 2014-2016 Tuscany Motorhomes for Fire Risk

    Thor Motor Coach is recalling 528 Tuscany motorhomes because water leaks into the keyless entry module, causing electrical shorts that increase fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0352-2017·2016-11-16

    Hershey Recalls SoFit Protein Plus Sunflower Seeds Due to Listeria Risk

    The Hershey Company is voluntarily recalling SoFit Protein Plus Sunflower Seeds because a supplier expanded its recall for potential Listeria monocytogenes contamination.

    Product
    SOFiT Protein Plus Sunflower Seeds Sea Salt; Seeds covered by a crunchy protein shell: NET WT. 1 OZ.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0354-2017·2016-11-16

    Hershey Recalls SoFit Protein Plus Pumpkin Seeds Due to Listeria Risk

    The Hershey Company is voluntarily recalling SoFit Protein Plus Pumpkin Seeds Sesame Garlic because a supplier expanded its recall of sunflower seeds, creating a potential Listeria monocytogenes contamination risk.

    Product
    SOFiT Protein Plus Pumpkin Seeds Sesame Garlic, Seeds covered by a crunchy protein shell: NET WT. 1 OZ.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0308-2017·2016-11-16

    Ev3 Neurovascular Alligator Retrieval Device Recalled for Coating Defect

    Micro Therapeutics Inc. is recalling 3,337 Alligator Retrieval Devices because the PTFE coating may delaminate and detach, potentially entering the bloodstream.

    Product
    Alligator Retrieval Device The device is intended for use in the peripheral and neurovasculature for foreign body removal. Catalog No. FA-88810-20V04 FA-88810-20V06 FA-88810-30V04 FA-88810-30V06 FA-88810-40V04 FA-88810-40V06 FA-88810-50V04 FA-88810-50V06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0353-2017·2016-11-16

    Hershey Recalls SoFit Protein Plus Almonds Due to Listeria Risk

    The Hershey Company is voluntarily recalling SoFit Protein Plus Almonds Jalapeno Garlic because a supplier expanded its recall of sunflower seeds, creating a potential Listeria monocytogenes contamination risk.

    Product
    SOFiT Protein Plus Almonds Jalapeno Garlic, whole almonds covered by a crunchy protein shell: NET WT. 1 OZ.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0307-2017·2016-11-16

    FDA Recalls Pipeline Embolization Devices Due to Coating Delamination

    Micro Therapeutics Inc is recalling Pipeline Embolization Devices because PTFE coating may delaminate and enter the bloodstream.

    Product
    Pipeline Embolization Device (Pipeline Classic) The device is indicated for the endovascular treatment of adults (22 year of age or older) with large or giant widenecked intracranial aneurysms (lAs) in the internal carotid artery from the petrous to the superior hypophyseal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0310-2017·2016-11-16

    Ev3 Neurovascular Recalls X-Celerator Hydrophilic Exchange Guidewires

    Micro Therapeutics Inc is recalling X-Celerator Hydrophilic Exchange Guidewires because PTFE coating delamination may release material into the bloodstream.

    Product
    X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0351-2017·2016-11-16

    Professional Botanicals Recalls MealPlex and Pearl Drinks for Undeclared Milk

    Professional Botanicals is recalling specific lots of MealPlex and Pearl meal drinks because they contain undeclared milk, a major food allergen.

    Product
    Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0 (378 grams) Ultimate Meal Drinks in Plastic Tub Containers. Dietary Supplement.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0374-2017·2016-11-16

    Siemens SOMATOM Definition Flash CT Systems Recalled for Injury Risk

    Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition Flash system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0373-2017·2016-11-16

    Siemens SOMATOM Definition AS CT Systems Recalled for Injury Risk

    Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition AS system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0325-2017·2016-11-16

    On the Border Tortilla Chips Recalled for Possible Metal Fragments

    Truco Enterprises is recalling On the Border Cafe Style Tortilla Chips due to possible metal fragments in the corn flour.

    Product
    On the Border Cafe Style Tortilla Chips 18 oz. and 28 oz. packaged in laminated polypropylene film with windows.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0378-2017·2016-11-16

    Stryker Recalls LFIT Anatomic V40 Femoral Heads Due to Taper Lock Failure

    Stryker Howmedica Osteonics is recalling specific lots of LFIT Anatomic V40 Femoral Heads because of reported taper lock failures that caused harm.

    Product
    LFIT Anatomic V40 Femoral Head, Low Friction Ion Treatment, Sterile, 36 mm, REF 6260-9-236; Modular components designed to be locked onto a femoral hip stem trunnion during surgery for total hip replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0309-2017·2016-11-16

    Ev3 Neurovascular Recalls Marathon and UltraFlow Micro Catheters

    Micro Therapeutics Inc. is recalling Marathon and UltraFlow HPC Flow Directed Micro Catheters because PTFE coating may delaminate and enter the bloodstream.

    Product
    Marathon Flow Directed Micro Catheter, UltraFlow HPC Flow Directed Micro Catheter Marathon Flow: The device is intended to access periphera and neurovasculature for the controlled selective infusion of physician-specified therapeutics agents such as embolization materials and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0390-2017·2016-11-16

    Maquet Accessory Adapter Recalled Due to Head Rest Slipping Hazard

    Maquet Medical Systems USA is recalling Accessory Adapter part number 600525A0 because a head rest mounted to the device slipped out of the mounting rail.

    Product
    Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail guide interface immediately before, during and after surgical interventions as well as for examination and treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0362-2017·2016-11-16

    Hospira Symbiq Infusion Pump Recall for White Screen Safety Shutdown

    Hospira is recalling Symbiq Two Channel Infusers that may display a white screen, causing the device to stop infusion and sound an alarm, which can delay or interrupt therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List number 16027. Note that Hospira retired this pump June 30, 2015. The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0285-2017·2016-11-16

    Koffee Kup Hamburger Buns Recalled for Plastic Contamination

    Koffee Kup Bakery is recalling hamburger buns in multiple states due to potential plastic pieces.

    Product
    Koffee Kup Hamburger Buns- White, Wheat, Seeded -3 1/2" 4", 5", packaged 16 oz. 18, oz, 20 oz, 25 oz, 29 oz
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0391-2017·2016-11-16

    Trumpf Medical Systems Recalls Operating Room Table Tops for Cable Pinching

    Trumpf Medical Systems is recalling specific operating room table tops after identifying six incidents of pinched cables.

    Product
    OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794; OR Table Top U24 H V, Model # 1909796; OR Table Top U24 H V U, Model # 1909797; OR Table Top U24 H V W, Model # 1909798; OR Table Top U14 H V, Model # 1909799 Product Usage: Patient positioning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0288-2017·2016-11-16

    Koffee Kup Hot Dog Buns Recalled for Plastic Contamination

    Koffee Kup Bakery Inc. is recalling hot dog buns because they may contain plastic pieces. Consumers should stop eating the product.

    Product
    Koffee Kup Hot Dog Buns- 8 pk and 16 pk
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0370-2017·2016-11-16

    Baxter Recalls Revaclear MAX Dialyzers Due to Potential Particulate Matter

    Baxter Healthcare is recalling 22,656 Revaclear MAX dialyzers because of potential particulate matter on the blood side of the device.

    Product
    GAMBRO Capillary Dialyzer, Polyflux(R) Revaclear MAX, STERILE, Product code 110634 Product Usage: The Revaclear Max dialyzer is a single use device used for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide