The Recall Desk

State

Rhode Island product recalls

73,741 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.

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36451–36475 of 76794

  • SevereFDA (Devices)·Z-0926-2019·2019-03-06

    Philips MR RT MRI Systems Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling MR RT MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V188000·2019-03-06

    Volkswagen Recalls 56,173 Vehicles for Rear Coil Spring Fracture Risk

    Volkswagen is recalling 56,173 vehicles because rear coil springs may fracture prematurely, potentially causing tire damage and loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, JETTA, GOLF SPORTWAGEN, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V178000·2019-03-06

    Entegra Recalls 2019-2020 Reatta Motorhomes for Damaged Tow Hitch

    Entegra Coach is recalling 2019-2020 Reatta motorhomes because the tow hitch may have been damaged during delivery, increasing the risk of a crash.

    Product
    ENTEGRA — ENTEGRA REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0895-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T, Model Number 781195. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1123-2019·2019-03-06

    Whole Foods Market Recalls Mesclun Mix Due to Salmonella Contamination

    Whole Foods Market is recalling Mesclun Mix With Candied Pecans and Sun Dried Cranberries due to potential Salmonella contamination. The product was distributed in eight northeastern and southeastern states.

    Product
    Mesclun Mix With Candied Pecans and Sun Dried Cranberries packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0873-2019·2019-03-06

    Philips Multiva MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Multiva MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1104-2019·2019-03-06

    Whole Foods Quinoa with Dark Leafy Greens Recalled for Salmonella Risk

    Whole Foods Market is recalling Quinoa with Dark Leafy Greens due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Quinoa with Dark Leafy Greens packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0876-2019·2019-03-06

    Philips Intera 1.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V177000·2019-03-06

    Jayco Recalls 2019-2020 Embark Motorhomes Due to Hitch Damage

    Jayco is recalling 2019-2020 Embark motorhomes because the hitch may have been damaged during delivery, increasing the risk of a crash if the towed vehicle separates.

    Product
    JAYCO — JAYCO EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1116-2019·2019-03-06

    Whole Foods Recalls Breakfast Sandwich Platters Due to Salmonella Risk

    Whole Foods Market is recalling Breakfast Sandwich Platters packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Breakfast Sandwich Platter packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1121-2019·2019-03-06

    Whole Foods Market Recalls Large Goat Cheese Green Salad for Salmonella Risk

    Whole Foods Market is recalling Large Goat Cheese Green Salad due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Large Goat Cheese Green Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0915-2019·2019-03-06

    Philips Achieva 1.5T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 1.5T Conversion, Model Number 781346. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0901-2019·2019-03-06

    Philips Ingenia MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling Ingenia 1.5T CX MRI systems because ceiling speakers may be pulled by the magnetic field and fall.

    Product
    Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0918-2019·2019-03-06

    Philips Ingenia 3.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1107-2019·2019-03-06

    Whole Foods Spinach Ravioli Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Spinach Ravioli Salad with Lemon, Tomato, and Parmesan due to potential Salmonella contamination.

    Product
    Spinach Ravioli Salad with Lemon, Tomato, and Parmesan packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0916-2019·2019-03-06

    Philips Ingenia 1.5T S MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 1.5T S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0885-2019·2019-03-06

    Philips Intera IT MRI Systems Recalled for Falling Ceiling Speaker Risk

    Philips is recalling 11,226 Intera IT MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0904-2019·2019-03-06

    Philips Ingenia 3.0T CX MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 3.0T CX MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0897-2019·2019-03-06

    Philips Achieva 7.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 7.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0875-2019·2019-03-06

    Philips MRI Systems Recalled Due to Ceiling Speaker Fall Risk

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0948-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.

    Product
    AF 550 x 5ML/HR 2ML 60LO CPNB, Product code MT5060XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V168000·2019-03-06

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Incorrect Weight Label

    Highland Ridge RV is recalling 74 units of 2019 Mesa Ridge and Open Range Ultra Lite travel trailers because the weight label exceeds the safety chain rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0953-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling specific Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF w/AS 550 x 1-14 ml/hr, 5ml30 LOCPNB, Product code MVBX30XLCPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0943-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF550x5ML/H 2ML 60LO 6" DUAL CATHS, 4.5", Product MT5060XLYK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide