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.

Which agencies issued them

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.

57601–57625 of 76887

  • ModerateFDA (Devices)·Z-1114-2015·2015-02-18

    Arthrosurface Shoulder Prosthesis Components Recalled for Lack of US Clearance

    Arthrosurface, Inc. is recalling 187 units of the HHXL (OVO) 15.6x32mm Taper Post Fixation Component because the product was not cleared for marketing in the US with its current indications.

    Product
    Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component; Catalog Number: 8156-0032, Part Number: 156-0032. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1067-2015·2015-02-18

    Natus Medical Recalls EPWorks Software Due to Remote Monitoring Error

    Natus Medical is recalling EPWorks software versions prior to 6.0 because a software error prevents remote users from stopping free run waveform groups.

    Product
    EPWorks software used in the Protektor 32 Product Usage: Uses electroencephalography (EEG), evoked potentials (EP), electromyography (EMG) and transcranial motor evoked potentials (TcMEP) stimulation techniques to provide healthcare professionals with information to help…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1080-2015·2015-02-18

    Arrow Epidural Needle Component Recalled for Missing Shelf Life Labeling

    Arrow International Inc. is recalling 63,022 units of ARROW Epidural Needle Components because the product labeling does not specify the 5-year shelf life.

    Product
    ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are used as a conduit for epidural catheter placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1081-2015·2015-02-18

    Lacrimedics Recalls VisiPlugST Devices Due to Moisture-Related Breakage

    Lacrimedics Inc is recalling VisiPlugST devices because moisture levels may cause the plugs to break apart or crumble upon contact.

    Product
    VisiPlugST for the Lacrimal Efficiency Test. It is also sold in the EU as CollaSyn Plugs. Model number 1813, 1814, 1815, 1903, 1904, and 1905. This device is cylindrical in shape, approximately 1.75-2.00mm in length, and available in three sizes: 0.3mm, 0.4mm and 0.5mm.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1077-2015·2015-02-18

    Stryker Flyte Toga Recall Due to Incorrect Expiration Date Labeling

    Stryker is recalling Flyte Togas with an incorrect expiration date. The label reads 2412-12-01 instead of 2014-12-01.

    Product
    Flyte Togas are components of the Stryker Flyte System and are intended to be worn over any Stryker Flyte Helmet. This toga provides Level 1 and 4 protection according to the Association for the Advancement of Medical Instrumentation (AAMI) Liquid Barrier Performance and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V088000·2015-02-13

    Mercedes-Benz Recalls Vehicles Due to Hood Seal Fire Risk

    Mercedes-Benz is recalling 2013-2015 E-Class and CLS-Class vehicles because a rubber seal may fall into the engine bay and contact the exhaust system, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS63, E350, CLS550, E63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E008000·2015-02-13

    Recaro Bus Driver Seats Recalled for Seat Belt Retraction Defect

    Johnson Controls is recalling Recaro bus driver seats where a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in crashes.

    Product
    SEAT BELTS:FRONT:RETRACTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E007000·2015-02-13

    Airtex Fuel Pump Modules Recalled Due to Fuel Leak Fire Risk

    Airtex is recalling specific fuel pump modules because an improper seal may cause fuel leaks, increasing the risk of a fire.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15070·2015-02-12

    Jackco ZETA Pocket Jump Starter Recalled for Fire Hazard

    Jackco Transnational is recalling ZETA Pocket Jump Starters because the battery packs can overheat and catch fire. Consumers should stop using the product and contact the company for a refund.

    Product
    ZETA by Jackco Pocket Jump Starter - Deluxe Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1059-2015·2015-02-11

    Siemens LINAC Accelerators Recalled for Overheating and Smoke Emission

    Siemens Medical Solutions is recalling 310 LINAC Accelerators because the internal electric board may overheat, causing thermal damage and smoke emission.

    Product
    LINAC Accelerators: ARTISTE, ONCOR Avant Garde, ONCOR Impression Plus, ONCOR Expression, ONCOR Impression, PRIMUS HI, Mevatron M2/Primus Mid-Energy, MEVATRON PRIMART, MEVATRON KD-2, MEVATRON KDS-2, MEVATRON KDS-2, MEVATRON KD-2, MEVATRON K2, MEVATRON 6323-2, MEVATRON…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V084000·2015-02-11

    Navistar Recalls 2015-2016 IC CE School Buses for Fuel Leak Risk

    Navistar is recalling 6,302 model year 2015-2016 IC CE school buses because the powertrain wiring harness may contact a high-pressure fuel line, potentially causing a fuel leak and fire.

    Product
    IC BUS — IC BUS CASB, CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1054-2015·2015-02-11

    Cardinal Health Recalls Lubricated Intubating Stylets Due to Shear Risk

    Cardinal Health is recalling 104,432 Lubricated Intubating Stylets 6FR because a small piece of the sheath may shear off during removal, posing a risk to infants and pediatric patients.

    Product
    Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and pediatric patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1017-2015·2015-02-11

    FDA Recalls Covidien Trellis-6 Peripheral Infusion Systems Due to Labeling Error

    The FDA is recalling 216 units of the Covidien Trellis-6 Peripheral Infusion System because a manufacturing error caused the balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0958-2015·2015-02-11

    Reily Foods Recalls Chili Kits for Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Wick Fowler's Famous Texas Style 2-Alarm Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit, NET WT. 3.6525 oz. (102g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-71092-00069-8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0956-2015·2015-02-11

    Reily Foods Recalls Chili Kits With Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT, NET WT. 4 oz. (113 g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-72396-10000-8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V086000·2015-02-11

    Airstream Recalls 2014-2015 Travel Trailers Due to Propane Tank Screw Failure

    Airstream is recalling 2014-2015 travel trailers because screws securing the propane tank tray may fail, allowing tanks to fall and cause fire or collision.

    Product
    AIRSTREAM — AIRSTREAM FLYING CLOUD, INTERNATIONAL, LAND YACHT, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide