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.

Which agencies issued them

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.

51476–51500 of 76878

  • HighFDA (Devices)·Z-1245-2016·2016-03-30

    Nidek RT-5100 and RT-3100 Refractors Recalled for Arm Malfunction

    Nidek Inc is recalling RT-5100 and RT-3100 refractors because the Near Point Chart Arm may lower spontaneously, posing a risk of slight injury to the patient's face or nose.

    Product
    RT-5100 (Epic 5100) Refractor and RT 3100 Refractor: Product Usage: Instrument providing means of positioning spherical and cylindrical lenses, prisms and other optical devices in front of a subjects eye for purpose of determining refractive error and binocular functions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1229-2016·2016-03-30

    Castile Soap Towelettes Recalled Due to Bacterial Contamination

    Covidien LLC is recalling Castile soap towelettes used in Foley trays and specimen kits because they are contaminated with bacteria.

    Product
    Covidien Dover PREC PRM 18FR SILVER FLY TY Item Code: PP18XSD Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1208-2016·2016-03-30

    Castile Soap Towelettes Recalled Due to Bacterial Contamination

    FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.

    Product
    Covidien Dover P400 UM 16FR SIL COUDE SECURE Item Code: P4P16CSDK Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1210-2016·2016-03-30

    Castile Soap Towelettes Recalled Due to Bacterial Contamination

    The FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.

    Product
    Covidien Dover P400 PREM U/M 16FR TMP SNS CSD Item Code: P4P16TSD Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1204-2016·2016-03-30

    Recall of Bacteria-Contaminated Castile Soap Towelettes in Medical Kits

    FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.

    Product
    Covidien Dover PREM U/M 14FR SIL FLY Item Code: P4P14SD P400 Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1202-2016·2016-03-30

    Recall of Contaminated Castile Soap Towelettes in Medical Kits

    FDA is recalling specific lots of Castile soap towelettes used in medical kits due to bacterial contamination.

    Product
    Covidien Dover MIDSTREAM KIT RING CASTILE Item Code: 4090SA Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1239-2016·2016-03-30

    CareFusion Recalls Alaris PC Infusion Pump Units Due to Power Supply Error

    CareFusion is recalling 170 Alaris PC Unit Infusion Pump Model 8000 devices because a power supply component may cause system error codes.

    Product
    Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1175-2016·2016-03-30

    Toshiba DRAD-3000E Wireless System Recalled for Image Transmission Failure

    Toshiba is recalling 28 DRAD-3000E FPD Wireless Systems because they fail to complete image transmission, resulting in no radiographic image.

    Product
    Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000¿ is intended for use with the ceiling-suspended tube support, high voltage generator, and bucky stand or bucky table incorporating a fixed or detachable (portable) flat panel detector for radiography of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1243-2016·2016-03-30

    Siemens IMMULITE 2000 Estradiol Test Recalled Due to Faslodex Interference

    Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Estradiol Test kits because the drug fulvestrant (Faslodex) may cause falsely elevated estradiol results.

    Product
    IMMULITE 2000 EstradiolTest Code E2 Catalog Number: L2KE22, L2KE22 (D), L2KE26, L2KE26 (D) SMN: 10381178, 10702833, 10381177, 10702834 Product Usage: For in vitro diagnostic use the IMMULITE¿2000 systems Analyzers- for the quantitative measurement of estradiol in serum, as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2016·2016-03-30

    Zimmer Spine Universal Clamp System Recall for Updated Cleaning Instructions

    Zimmer Spine is issuing a correction notice for the Universal Clamp System to provide updated cleaning and disinfecting instructions.

    Product
    Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and helps reduce spinal deformities and fractures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0781-2016·2016-03-30

    AstraZeneca Recalls Tudorza Pressair Inhalers Due to Defective Delivery System

    AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.

    Product
    Tudorza Pressair (aclindinium bromide inhalation powder), 400 mcg per actuation, 60 Metered Doses per Inhaler, Rx Only. Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850. Manufactured by: Forest Laboratories, Ireland Limited, Dublin 17 Ireland. Product of…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1232-2016·2016-03-30

    Siemens syngo X Workplace Medical Workstation Recalled for Segmentation Error

    Siemens Medical Solutions USA is recalling six syngo X Workplace medical workstations because imported segmentation results appear mirrored, rendering them unusable for ablation procedures.

    Product
    syngo X Workplace is a medical workstation for real-time viewing, image manipulation, 3D-visualization, communication, and storage of medical images and data on exchange media. It is used for diagnostic image viewing and post processing during interventional procedures. .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1240-2016·2016-03-30

    Siemens Estradiol Test Recalled Due to Potential False Results

    Siemens is recalling ADVIA Centaur Enhance Estradiol tests because the drug fulvestrant may cause falsely elevated results.

    Product
    Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number: 10490889, 10491445, 10697757 Product Usage: For in vitro diagnostic use in the quantitative determination of estradiol in human serum and plasma (heparinized and EDTA) using the ADVIA Centaur¿, ADVIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1190-2016·2016-03-30

    Zimmer Biomet Issues Correction Notice for Instinct Java System Cleaning Instructions

    Zimmer Biomet is issuing a correction notice to provide updated cleaning and disinfecting instructions for the Instinct Java System and Universal Clamp System.

    Product
    Instinct¿ Java¿ System (IFU reference: 046WAN0000T) . Stabilizes one or more vertebral segments from the thoracic spine to the sacrum during the development of bone tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1247-2016·2016-03-30

    Neurotherm Curved Radiofrequency Cannula Recalled for Mislabeling

    Neurotherm, Inc. is recalling 135 curved radiofrequency cannulas because straight needles were incorrectly labeled as curved.

    Product
    Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of radiofrequency energy with as intended result, thermo coagulation of nervous tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0773-2016·2016-03-30

    ShopRite Unsalted Dry Roasted Cashews Recalled for Mislabeling

    Wakefern Foods Corp. is recalling ShopRite Unsalted Dry Roasted Cashews because the product may be mislabeled.

    Product
    ShopRite Dry Roasted Unsalted Cashews 7 oz. (198 g) Distributed by Wakefern Food Corp., Elizabeth, NJ 07207 UPC 4119001620
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·16V176000·2016-03-29

    Forest River Georgetown RVs Recalled for Missing Emergency Egress Window

    Forest River is recalling 2015-2017 Georgetown RVs because a vented window was installed instead of a required secondary egress window, posing a risk of entrapment.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V175000·2016-03-29

    Forest River Recalls 2013-2016 Puma Trailers for Tire Clearance Issue

    Forest River is recalling 2013-2016 Puma recreational trailers because tires may contact the wheel well on bumps, risking tire damage and loss of control.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V177000·2016-03-29

    Terex Recalls 2011-2016 Aerial Devices Due to Inadequate Boom Tip Welds

    Terex is recalling 2011-2016 aerial devices because inadequate welds at the boom tip may cause the platform to tilt unexpectedly, increasing the risk of user injury.

    Product
    TEREX — TEREX AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16124·2016-03-28

    Fiskars 32-Inch Bypass Lopper Shears Recalled for Laceration Hazard

    CPSC reannounced the recall of Fiskars 32-inch bypass lopper shears after additional injuries were reported. Consumers should stop using the product and contact Fiskars for a free replacement.

    Product
    Fiskars® 32-Inch Bypass Lopper Shears
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V173000·2016-03-25

    BMW Recalls 2016 7 Series Vehicles Due to Air Bag Control Module Defect

    BMW is recalling 6,110 model year 2016 740Li, 750Li, and 750Lxi vehicles because the air bag control module may reset, preventing air bags from deploying in a crash.

    Product
    BMW — BMW 750LI, 750LXI, 740LI
    Category
    Vehicle
    Distribution
    Distributed nationwide