The Recall Desk

State

Rhode Island product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50776–50800 of 76878

  • HighNHTSA·16V294000·2016-05-12

    Kovatch Mobile Equipment Recalls Firefighting Vehicles Due to Pump Strainer Defect

    Kovatch Mobile Equipment is recalling certain 2016-2017 emergency vehicles because pump intake strainers may be improperly soldered, potentially causing pump damage and reduced firefighting effectiveness.

    Product
    NAVISTAR — NAVISTAR, KME 4400, 7400, PREDATOR SS, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V296000·2016-05-12

    Supreme Recalls 2011-2014 Vans Due to Fire Risk in Marker Lights

    Supreme Corporation is recalling 2011-2014 Signature Van, Iner-City, and Kold King vehicles because roof marker lights may short circuit and cause the corner caps to catch fire.

    Product
    SUPREME — SUPREME KOLD KING, SIGNATURE VAN, INER-CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1318-2016·2016-05-11

    Back To Nature Classic Creme Cookies Recalled for Undeclared Milk

    Back To Nature Foods is recalling Classic Creme Cookies because they contain undeclared milk. The recall covers 154,044 cartons shipped to 16 states.

    Product
    Classic Creme Cookies, Net wt. 12 oz cartons, 6 cartons per case. Manufactured for Back To Nature Foods Co., LLC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1535-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Conductivity Sensors Due to Leakage Risk

    B Braun Medical Inc is recalling 68 Dialog+ Hemodialysis Conductivity Sensors due to a potential leakage hazard. The units were distributed nationwide to various states and territories.

    Product
    Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health center and outpatient dialysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V291000·2016-05-11

    Keystone Recalls 2016-2017 Passport Trailers Due to Axle Defect

    Keystone RV Company is recalling specific 2016-2017 Passport trailers because they were built with axles that have lower capacity than required, increasing the risk of axle failure and a crash.

    Product
    KEYSTONE — KEYSTONE PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1531-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage Risk

    B Braun Medical Inc is recalling 370 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide and in Puerto Rico.

    Product
    Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L Serial # >200318 and < 2039222 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1536-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Conductivity Sensors Due to Leakage Risk

    B Braun Medical Inc is recalling 147 Dialog+ Hemodialysis Conductivity Sensors due to potential leakage. The sensors are used in dialysis machines for kidney failure patients.

    Product
    Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item 3456103A The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health center and outpatient dialysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1534-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage Risk

    B Braun Medical Inc is recalling 90 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.

    Product
    Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL-BIC Product Code # 710200U Serial # 202136 and < 203837 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V284000·2016-05-11

    2016 Jeep Cherokee Recall for Right Halfshaft Fracture Risk

    Chrysler is recalling 2016 Jeep Cherokee vehicles because the right halfshaft may fracture without warning, increasing crash risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1532-2016·2016-05-11

    B Braun Dialog+ Hemodialysis Machines Recalled for Potential Sensor Leakage

    B Braun Medical Inc. is recalling 40 Dialog+ Hemodialysis machines due to a potential leakage issue with conductivity sensors.

    Product
    Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Product Code 710200K Serial # >202169 and < 203249 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1533-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage

    B Braun Medical Inc is recalling 318 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.

    Product
    Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code # 710200S Serial # >200805 and <204001 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V292000·2016-05-11

    Subaru Recalls 2016-2017 Legacy and Outback for Steering Column Defect

    Subaru is recalling 48,819 Legacy and Outback vehicles because an improperly machined steering column may cause loss of steering control, increasing crash risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·040-2016·2016-05-11

    Ajinomoto Windsor Recalls Meat and Poultry Products Due to Listeria Risk

    Ajinomoto Windsor is recalling approximately 47 million pounds of not-ready-to-eat meat and poultry products due to possible Listeria monocytogenes contamination.

    Product
    Ajinomoto Windsor Inc. — Ajinomoto Windsor, Inc. Recalls Meat and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V285000·2016-05-11

    Forest River Recalls 2016-2017 Berkshire and Cross Country RVs for Sway Bar Defect

    Forest River is recalling specific 2016-2017 Berkshire and 2016 Cross Country recreational vehicles because front sway bar brackets may not fit properly, risking detachment and crashes.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1606-2016·2016-05-11

    CareFusion Alaris PC Unit Model 8015 Recalled for Power-Up Error

    CareFusion 303, Inc. is recalling 23,397 Alaris PC units, Model 8015, because a super capacitor failure may cause a system error code at power-up.

    Product
    Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V286000·2016-05-11

    Great Lakes Drywall Pup Trailers Recalled for Rear Impact Guard Defect

    Great Lakes is recalling 1998-2016 Drywall Pup trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.

    Product
    GREAT LAKES — GREAT LAKES DRYWALL PUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1598-2016·2016-05-11

    Siemens MAGNETOM MRI Systems Recalled Due to Magnetic Table Cover Hazard

    Siemens is recalling eight MAGNETOM Aera/Skyra MRI systems because the patient table's docking station cover may contain a magnetic plate that attracts to the main magnet.

    Product
    MAGNETOM Aera/Skyra Systems, whole body magnetic resonance imaging systems, Model numbers 10432914, 10432915. Docking station top cover (part no# 10591430) of the removable patient table.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1310-2016·2016-05-11

    Specialty Produce Recalls Diced Red Potatoes for Undeclared Sulfites

    Specialty Produce Corporation is recalling diced red potatoes in Rhode Island due to undeclared sulfites. The recall was initiated voluntarily by the firm.

    Product
    Diced Red Potatoes, hand labeled: "Potato, Red Dice, 40# 3/4 large"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1586-2016·2016-05-11

    Ab Sciex Analyst MD Software Recall for Incorrect Diagnostic Results

    Ab Sciex is recalling Analyst MD software versions 1.6.1 and 1.6.2 because it may display wrong quantitative results, potentially leading to incorrect patient diagnoses.

    Product
    Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/MS System, Instrument Part Number: 5024501; 3200MD QTRAP¿ LC/MS/MS System, Instrument Part Number: 5024500; Triple Quad" 4500MD LC/MS/MS System, Instrument Part Number: 5031257…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1601-2016·2016-05-11

    Siemens Syngo Dynamics PACS Software Recall for Workflow Error

    Siemens is recalling 84 units of Syngo Dynamics software due to a defect that may cause old measurements to be carried forward into new reports.

    Product
    Syngo Dynamics; Kinetdx Picture Archiving and Communications System
    Category
    Medical Device
    Distribution
    Distributed nationwide