The Recall Desk

State

Rhode Island product recalls

73,100 recalls have nationwide distribution and so reach Rhode Island. 3,046 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,046
Critical
221
Severe
572
Most recent
2026-09-23

Of the 3,046 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 572 (19%) are Severe.

These figures cover only the 3,046 recalls whose distribution notice names Rhode Island specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10976–11000 of 76146

  • HighNHTSA·24V511000·2024-07-03

    Freightliner Custom Chassis S2C and S2RV Brake Light Recall

    Daimler Trucks North America is recalling 2023-2025 Freightliner Custom Chassis S2C and S2RV trucks because brake lights may not illuminate during active brake assist events.

    Product
    FCCC — FCCC S2C, S2RV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2186-2024·2024-07-03

    Siemens Multix TOP X-ray Table Recalled Due to Fire Risk

    Siemens is recalling 3 Multix TOP I PRO radiographic X-ray tables due to a short circuit in the Touch Display power supply unit that may cause overheating and fire.

    Product
    MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2190-2024·2024-07-03

    Medtronic Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic recalled 14 COBALT HF QUAD CRT-D MRI SureScan implantable defibrillators due to a weld crack manufacturing defect detected during quality control testing.

    Product
    COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2211-2024·2024-07-03

    Medtronic ICD Implants Recalled for Manufacturing Weld Crack Defects

    Medtronic recalls 9 units of CROME VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality control leak testing.

    Product
    CROME VR MRI SureScan, Model Number DVPC3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2202-2024·2024-07-03

    Implantable Cardioverter Defibrillator Recalled Due to Manufacturing Weld Defect

    Medtronic is recalling 26 MIRRO MRI DR SureScan Implantable Cardioverter Defibrillators due to a manufacturing defect involving a weld crack that could affect device function.

    Product
    MIRRO MRI DR SureScan, Model Number DDME3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2175-2024·2024-07-03

    Endoscopic Vessel Harvesting System Recalled Due to Potential Cautery Malfunction

    Maquet Cardiovascular recalls VasoView HemoPro 2 vessel harvesting systems due to potential fluid ingress that may prevent or unintentionally activate cautery function. The recall affects 430,037 units distributed worldwide.

    Product
    The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model Number: VH-4000. 2. VasoView Hemopro 2 with Vasoshield. Model Number: VH-4001. The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting Systems are designed for use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0564-2024·2024-07-03

    Buprenorphine Injection Recalled Due to Incomplete Seal Integrity Issue

    Pfizer is recalling specific lots of Buprenorphine Hydrochloride Injection due to potential incomplete crimp seals that could compromise product sterility. Patients using affected lots should consult their healthcare provider.

    Product
    BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2208-2024·2024-07-03

    Medtronic COBALT VR MRI SureScan implantable defibrillators recalled for manufacturing defect

    Medtronic is recalling 4 COBALT VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing defect involving a weld crack identified during quality control testing.

    Product
    COBALT VR MRI SureScan, Model Number DVPB3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2173-2024·2024-07-03

    Sight OLO CBC Test Kit Lot Recalled for Bacterial Contamination

    One lot of Sight OLO CBC Test Kit is being recalled due to bacterial contamination that causes artificially elevated platelet counts. The affected kits may produce inaccurate test results.

    Product
    Sight OLO CBC Test Kit, Model/Catalog Number: TK1. A disposable cartridge and sample preparation tools for use with the Sight OLO CBC analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2216-2024·2024-07-03

    NovaGuide 2 Ultrasound Systems Recalled for Electrical Shock Risk

    FDA is recalling 45 NovaGuide 2 Intelligent Ultrasound systems due to a defective grounding cable that could become disconnected and cause electrical shock, electrical interference, or equipment malfunction.

    Product
    NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2024·2024-07-03

    CDC Influenza H5 Subtyping Kit may produce inconclusive test results

    The CDC Influenza A/H5 Subtyping Kit's H5b component may fail to amplify, resulting in inconclusive results. 191 units were distributed nationwide.

    Product
    CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2024·2024-07-03

    Sonic Scaler Tip Holder May Be Oversized, Preventing Proper Seating

    The tip holder portion of Titan Blis-Sonic Scaler tips may be oversized, preventing proper seating in the scaler handpiece. This defect could result in the tip becoming loose during use.

    Product
    Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio (part number 261669) (1) P/N 264563 (2) P/N 264565 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0569-2024·2024-07-03

    SinuFrin Nasal Decongestant Recalled for Sub-Potency Nationwide

    NeilMed Pharmaceuticals is recalling 20,370 bottles of SinuFrin Quick Relief Decongestant (Lot SD134) nationwide due to sub-potency. No illnesses have been reported.

    Product
    SINUFRIN QUICK RELIEF DECONGESTANT — SINUFRIN QUICK RELIEF DECONGESTANT (SINUFRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V504000·2024-07-02

    Mack Trucks Recalls 2025 Models Due to Tie Rod Assembly Defect

    Mack Trucks is recalling 2025 LR, Granite, and Pinnacle vehicles because a tie rod assembly ball stud may fail, creating a road hazard and increasing crash risk.

    Product
    MACK — MACK PIONEER PR (4), GRANITE (GR), LR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V499000·2024-07-02

    2023-2024 Fisker Ocean recalled for sudden loss of drive power

    A battery management system failure in 2023-2024 Fisker Ocean vehicles can cause sudden loss of drive power. Fisker will replace the affected pumps at no cost.

    Product
    FISKER — FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V500000·2024-07-02

    ARBOC Spirit of Freedom Recalled for Seat Recliner Defect

    ARBOC is recalling 2023-2024 Spirit of Freedom vehicles because the seat recliner mechanism may not engage, increasing injury risk in a crash.

    Product
    ARBOC — ARBOC SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V502000·2024-07-02

    Starcraft Starlite Buses Recalled for Inaccessible Emergency Exit Handles

    Forest River is recalling 2023-2024 Starcraft Starlite buses because emergency exit handles are not easily accessible, potentially delaying passenger evacuation during emergencies.

    Product
    STARCRAFT BUS — STARCRAFT BUS STARLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V507000·2024-07-02

    Spartan Fire Recalls Fire Apparatus Due to Brittle Suspension Bolts

    Spartan Fire is recalling 2023-2025 Gladiator, Metro Star, and KME Panther vehicles because lower control arm bolts may break and become projectiles.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME GLADIATOR, METROSTAR, PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V501000·2024-07-02

    E-One Recalls 2024 Cyclone N and Typhoon N for Suspension Bolt Defect

    E-One is recalling 2024 Cyclone N and Typhoon N vehicles because lower front suspension control arm bolts may become brittle and break, posing an injury risk.

    Product
    E-ONE — E-ONE CYCLONE N, TYPHOON N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V503000·2024-07-02

    Volvo Recalls 2025 VHD and VN Trucks for Tie Rod Defect

    Volvo Trucks is recalling 2025 VHD and VN trucks because a tie rod ball stud may fail, creating a road hazard and increasing crash risk.

    Product
    VOLVO — VOLVO VHD, VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V498000·2024-07-01

    2024 Nissan Sentra windshield air bubbles obscure vehicle identification number

    Certain 2024 Nissan Sentra vehicles have windshield air bubbles on the front lower driver's side that can obscure the Vehicle Identification Number. This defect prevents owners from clearly identifying their vehicle and may prevent recall recognition.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V497000·2024-07-01

    2022–2023 Lucid Air vehicles recalled for software fault causing loss of drive power

    Lucid is recalling certain 2022 and 2023 Air vehicles due to a software fault that could disconnect the high voltage system while driving, causing loss of drive power and increasing crash risk. A free over-the-air software update is available.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2024·2024-06-30

    Michael Foods Recalls Liquid Egg Products Due to Undeclared Milk Allergen

    Michael Foods is recalling approximately 4,620 pounds of liquid egg products because they contain undeclared milk, a known allergen. The products were shipped to restaurant consignees in nine states.

    Product
    M.G. Waldbaum Company — Michael Foods Inc. Recalls Fair Meadow Foundations Liquid Egg Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide