The Recall Desk

State

Rhode Island product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57151–57175 of 76887

  • HighFDA (Devices)·Z-1310-2015·2015-04-01

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software due to an issue with photon dose calculation for Dynamic MLC plans.

    Product
    RayStation Radiation Therapy Treatment Planning System; -- RayStation 3.5, RayStation 4.0, RayStation 4.5 and RayStation 4.7. For RayStation 4.7, the issue applies also to machines with fixed jaws, regardless of MLC/jaw position. RayStation is a software system designed for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1306-2015·2015-04-01

    Penner Patient Stretcher/Transfer Lift System Recalled for Tipping Hazard

    Penner Mfg Inc is recalling 158 Patient Stretcher/Transfer Lift Systems because improper patient positioning could cause the device to tip, risking injury to patients or operators.

    Product
    Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in nursing homes, hospitals, and assisted living facilities to transfer and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1327-2015·2015-04-01

    Ameda Dual Short Term HygieniKit Milk Collections System Recalled for Lack of Sterilization

    Ameda is recalling its Dual Short Term HygieniKit Milk Collections System because the devices were not sterilized. Consumers should stop using the product and contact the manufacturer.

    Product
    Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115) - Primary packaging is 12 pouches with Tyvek header (10.75 x 16.375 x 3") within a secondary corrugated shipper (20.75 x 15.50 x 8.5" inner dimensions). The device is intended to be connected to a powered…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1304-2015·2015-04-01

    Intuitive Surgical Recalls da Vinci Xi Systems Due to Sensor Fault

    Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide due to a fault causing distal SUJ failures and position sensor mismatches.

    Product
    da Vinci Xi Surgical System, IS4000; ASSY,USM,IS4000, Material number: 380647-20 and 380647-22 The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endocopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2015·2015-04-01

    Siemens MAGNETOM MRI Systems Recalled for Gradient Output Supervision Defect

    Siemens Medical Solutions is recalling 132 MAGNETOM MRI systems because a defect in gradient output supervision could allow outputs to exceed safety limits, potentially causing peripheral nerve stimulation.

    Product
    MAGNETOM systems Aera/Skyra/Avanto/Verio with software syngo MR D13A ; indicated for use as magnetic resonance diagnostic devices (MRDD) that produce transverse, sagittal, coronal and oblique cross-sectional images, spectroscopic images and/or spectra, and that display the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1577-2015·2015-04-01

    Uncle Ben's Ready Rice Recalled for Potential Metal Fragments

    Mars Food US is recalling Uncle Ben's Ready Rice New Orleans Style Red Beans & Rice due to the potential for containing metal fragments.

    Product
    UNCLE BEN'S(R) Ready Rice(R) NEW ORLEANS STYLE RED BEANS & RICE, with a blend of smokey, savory seasonings, Net Wt 8.5 oz (240 g),
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1628-2015·2015-04-01

    Taj Ethnic Gourmet Punjabi Saag Spinach Sauce Recalled for Undeclared Peanut

    The Hain Celestial Group is recalling Taj Ethnic Gourmet Punjabi Saag Spinach Sauce because it may contain undeclared peanut protein.

    Product
    Taj ETHNIC GOURMET PUNJAB SAAG Spinach Sauce, NET WT 16.0 OZ. (454.0g), UPC 7 18687 30013 8
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1311-2015·2015-04-01

    CareFusion Recalls Alaris PC Infusion Pumps Due to Keypad Error Code

    CareFusion 303, Inc. is recalling 56,015 Alaris PC infusion pumps because a keypad issue may trigger an error code during the power-on self-test.

    Product
    Alaris PC units, Model No. 8015. Infusion pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1313-2015·2015-04-01

    Synthes Electric Pen Drive Hand Switch Labeling Error Recall

    Synthes, Inc. is recalling 249 Electric Pen Drive systems because the Hand Switch labels for 'on' and 'lock' were interchanged.

    Product
    Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, decorticating, shaping, and smoothing of bones and teeth in a wide variety of surgical procedures, including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0420-2015·2015-04-01

    West-Ward Recalls Fentanyl Citrate Injections Due to Impurity Failures

    West-Ward Pharmaceutical is recalling Fentanyl Citrate injections because the product failed impurity and degradation specifications and 12-month stability testing.

    Product
    FENTANYL CITRATE — FENTANYL CITRATE (FENTANYL CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1323-2015·2015-04-01

    ArthroCare Recalls 15 Coblator II Systems Due to Component Reversal

    ArthroCare Medical Corporation is recalling 15 Coblator II systems because specific components were reversed on the controller boards.

    Product
    Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgical system designed for use in otorhinolaryngology (ENT) surgery. The system consists of the following components: an electrosurgical radiofrequency controller…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1321-2015·2015-04-01

    Siemens ADVIA Chemistry Systems Drug Calibrator I Recalled for Incorrect Values

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Systems Drug Calibrator I, lot 3JD018, due to incorrect calibrator values for Phenytoin 2 and Phenobarbital 2 assays.

    Product
    ADVIA Chemistry Systems Drug Calibrator I; For in vitro diagnostic use in the calibration of Phenobarbital_2 (PHNB_2), Phenytoin_2 (PHNY_2), and Theophylline_2 (THEO_2) methods on the ADVIA Chemistry systems. System Information: (For Information Only) The ADVIA Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1315-2015·2015-04-01

    Leica CD15 Antibody Recalled for Decreasing Staining Intensity

    Leica Microsystems is recalling 309 units of CD15 antibody because staining intensity decreases over shelf life.

    Product
    Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform immunohistochemical (IHC) staining. Product Usage: NCL-L-CD15 is intended for the qualitative identification by light microscopy of CD15 molecules in paraffin sections. The clinical interpretation of any…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V191000·2015-03-31

    Thor Motor Coach Recalls 2015 Siesta and Citation Motorhomes

    Thor Motor Coach is recalling 2015 Siesta and Citation motorhomes because an incorrectly installed door component may make doors harder to open after a crash.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH SIESTA, CITATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V192000·2015-03-31

    Smart Fortwo Recall Issued for Potential Steering Gear Bolt Failure

    Mercedes-Benz USA is recalling 2014-2015 Smart Fortwo vehicles because steering gear mounting bolts may break, increasing crash risk.

    Product
    SMART — SMART FORTWO CONVERTIBLE, FORTWO COUPE ELECTRIC, FORTWO COUPE, FORTWO CONVERTIBLE ELECTR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V189000·2015-03-31

    BMW Recalls 2014-2015 Models for Fuel Pump Defect

    BMW is recalling 18,054 vehicles due to a fuel pump defect that may cause the vehicle to stall without warning, increasing crash risk.

    Product
    BMW — BMW 428I, 435I, 328XI, 328I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15106·2015-03-31

    Blinds To Go Recalls Window Shades Due to Strangulation Hazard

    Blinds To Go is recalling about 200,000 custom-made window shades because the cord hold-down device can fail, posing a strangulation risk to small children.

    Product
    Blinds To Go custom-made window shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V188000·2015-03-31

    BMW Recalls 2013-2014 5 Series Vehicles for Rear Reflector Defect

    BMW is recalling certain 2013-2014 5 Series vehicles because rear reflex reflectors may not reflect enough light, increasing crash risk.

    Product
    BMW — BMW 525D XDRIVE, ACTIVE HYBRID 5, 535I, 535XI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V184000·2015-03-30

    MCI Motor Coaches Recalled for Improperly Torqued Tie Rod Nuts

    MCI is recalling 2014-2015 motor coaches because improperly torqued tie rod nuts may cause loss of vehicle control and increase crash risk.

    Product
    MCI — MCI D4500, J4500, D4005, D4000ISTV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E025000·2015-03-30

    Ohlins TTX36 Motorcycle Shock Absorber Recall for Loose Nut

    Ohlins is recalling TTX36 aftermarket motorcycle shock absorbers because the damper rod nut may loosen, potentially causing loss of vehicle control.

    Product
    SUSPENSION:REAR:SHOCK ABSORBER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide