The Recall Desk

State

Rhode Island product recalls

73,584 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,048
Critical
221
Severe
707
Most recent
2026-10-21

Of the 3,048 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 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25801–25825 of 76632

  • SevereFDA (Devices)·Z-1553-2021·2021-05-19

    ReWalk Robotics Recalls Powered Exoskeletons Due to Fire Risk

    Argo Medical Technologies is recalling ReWalk Personal and R Systems exoskeletons after reports that the waistpack battery packs caught fire while charging.

    Product
    ReWalk Personal 6.0, ReWalk Personal 5.0 and ReWalk R Systems orthotically fits to the lower limbs and part of the upper body and is intended to enable individuals with spinal cord injury at levels T7 to L5 to perform ambulatory functions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V366000·2021-05-19

    International and IC Bus commercial vehicles recalled for fuel rail assembly defect

    Navistar is recalling certain 2018-2021 International and IC Bus commercial vehicles due to a fuel rail assembly defect. A sealing washer may not seat correctly, allowing fuel leaks that could ignite.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS DURASTAR, WORKSTAR, HV, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0791-2021·2021-05-19

    Nature's Sunshine Recalls Vegan Meal Replacement for Potential Milk Traces

    Nature's Sunshine Products is recalling specific lots of Love & Peas Protein Rich Meal Replacement because an ingredient may contain traces of milk, despite the product being labeled vegan and dairy-free.

    Product
    Love & Peas Protein Rich Meal Replacement, 1 LB 8 OZ (675 G) bag, Nature's Sunshine Products, Inc., Spanish Fork, Utah, 84660 (800) 223-8225, naturessunshine.com, UPC 0 99904 03082 4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1554-2021·2021-05-19

    Medical Action Industries Recalls Central Line Dressing Change Kits

    Medical Action Industries is recalling Central Line Dressing Change Kits due to a potential breach in the package integrity of a component.

    Product
    Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1541-2021·2021-05-19

    Meridian Revogene RNA Software Upgrade Kits Recalled Due to False Negatives

    Meridian Bioscience is recalling 124 Revogene RNA Software Upgrade Kits because the FDA withdrew the Emergency Use Application after false negative results were reported.

    Product
    Revogene RNA Software Upgrade Kit Revogene RNA Software Upgrade USBs Catalog Number: 610240 IVD used to install the Revogene System Software version 4.2.0, import the Revogene Instrument Control Protocol file for RNA-based assay, and install the Assay Definition File (ADF)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V369000·2021-05-19

    2021–2022 Heavy-Duty Trucks Recalled for Loose Tie Rod Assembly Components

    Daimler Trucks North America is recalling certain 2021–2022 heavy-duty trucks including Freightliner and Western Star models due to potentially loose tie rod clamps. Loose or detached tie rod ends could cause steering loss and increase crash risk.

    Product
    FCCC — FCCC, WESTERN STAR, FREIGHTLINER XB CHASSIS, S2, MT CHASSIS, 5700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1530-2021·2021-05-19

    St. Jude Medical Recalls Assurity and Endurity Pacemakers Due to Moisture Ingress

    St. Jude Medical is recalling Assurity and Endurity pacemakers because a manufacturing issue with epoxy mixing may allow moisture to enter the device, potentially causing malfunction.

    Product
    ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to provide single-chamber or dual-chamber bradycardia pacing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1540-2021·2021-05-19

    Meridian Revogene SARS-CoV-2 Test Recalled Due to False Negative Results

    Meridian Bioscience is recalling 376 Revogene SARS-CoV-2 test kits because the FDA withdrew the Emergency Use Application after false negative results were reported.

    Product
    Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) qualitative test run on the Revogene¿ instrument for the detection of SARS-CoV-2 nucleic acid from nasopharyngeal swab (NPS) specimens from individuals…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1531-2021·2021-05-19

    St. Jude Medical Recalls Endurity Pacemakers Due to Epoxy Manufacturing Issue

    St. Jude Medical is recalling 95,042 Endurity pacemakers because a manufacturing issue with epoxy may allow moisture ingress, potentially causing device malfunction.

    Product
    ENDURITY Pulse Generator REF PM**** SN ********* St. Jude Medical Cardiac Rhythm Assurity and Endurity pacemakers are intended to provide single-chamber or dual-chamber bradycardia pacing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21137·2021-05-19

    Cheyenne Mainstay Folding Chairs and Barstools Recalled for Fall Hazard

    Cheyenne Products is recalling about 795,000 Mainstay folding chairs and barstools because a weld can break, posing a fall hazard. Consumers should stop using them and contact Cheyenne for a refund.

    Product
    Cheyenne Products Mainstay folding metal padded chairs and barstools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1547-2021·2021-05-19

    GE Healthcare Recalls NM/CT 870 DR Scanners for Radiation Exposure Shift

    GE Healthcare is recalling NM/CT 870 DR scanners because a specific workflow may cause a shift in CT radiation exposure range, potentially requiring patient re-scans.

    Product
    NM/CT 870 DR Nuclear Medicine / CT Scanners
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1548-2021·2021-05-19

    Atos Medical Recalls Provox Life Night HME Devices Due to Insertion Risk

    Atos Medical AB is recalling Provox Life Night HME devices because they may be incorrectly inserted, potentially blocking the patient's stoma.

    Product
    Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients breathing through a tracheostoma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1568-2021·2021-05-19

    ICU Medical Recalls Spinning Spiros Male Luers Due to Molding Defect

    ICU Medical is recalling specific lots of Spinning Spiros Closed Male Luers because a molding defect may cause leakage in the inactivated position.

    Product
    REF 20130-01 Spinning Spiros Closed Male Luer, Red Cap - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1552-2021·2021-05-19

    Bard PowerPort duo M.R.I. Implantable Port Recall for Catheter Issues

    Bard Peripheral Vascular Inc. is recalling 287 PowerPort duo M.R.I. Implantable Ports due to catheter flushing difficulties and septum dislodgement.

    Product
    PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 5829502, UDI: (01)00801741027406 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2021·2021-05-19

    ICU Medical Recalls Oncology Kits Due to Molding Defect

    ICU Medical is recalling specific lots of Oncology Kits with Spinning Spiros due to a molding defect that may cause leakage in the inactivated position.

    Product
    REF CL3946 Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port, Vented Cap; ChemoLock , Spinning Spiros w/Red Cap - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1545-2021·2021-05-19

    GE Healthcare Recalls NM/CT 850 Scanners Due to Radiation Exposure Shift

    GE Healthcare is recalling NM/CT 850 scanners because a specific workflow may cause a 5cm shift in CT radiation exposure, potentially requiring patient re-scans.

    Product
    NM/CT 850 Nuclear Medicine / CT Scanners
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1579-2021·2021-05-19

    ICU Medical Recalls Sprios Male Luer Administration Sets Due to Molding Defect

    ICU Medical is recalling specific lots of Sprios male luer administration sets due to a molding defect that may cause leakage in the inactivated position.

    Product
    REF CH3020 40" (102 cm) Appx. 4.8 ml, 20 Drop Admin Set w/In-Line Chamber, 2 Spiros", Hanger - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2021·2021-05-19

    ICU Medical Recalls Sprios IV Adapters Due to Leakage Defect

    ICU Medical is recalling specific lots of Sprios IV adapters because a molding defect may cause leakage in the inactivated position.

    Product
    REF 034-H2629 Appx 1.0 ml, Adaptador universal para sistemas IV con Spiros" - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V367000·2021-05-19

    Navistar Recalls 2019-2021 IC Bus RE School Buses for Fuel Leak Risk

    Navistar is recalling 2019-2021 IC Bus RE School Buses because a sealing washer may not seat correctly, causing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    IC BUS — IC BUS RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21136·2021-05-19

    IKEA Recalls PLA Bowls, Plates, and Mugs Due to Burn Hazard

    IKEA is recalling HEROISK and TALRIKA bowls, plates, and mugs made of PLA material because they can become brittle and break, causing hot contents to leak and burn consumers.

    Product
    IKEA Recalls Bowls, Plates, and Mugs Due to Burn Hazard
    Category
    Consumer Product
    Distribution
    Distributed nationwide