The Recall Desk

State

Rhode Island product recalls

73,737 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.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33451–33475 of 76790

  • SevereFDA (Devices)·Z-2313-2019·2019-09-18

    Teleflex Recalls Sheridan EZ-ENDO Tracheal Tubes Due to Disconnection Risk

    Teleflex Medical is recalling specific lots of Sheridan EZ-ENDO tracheal tubes because the 15 mm connector may disconnect, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-22515 e) 8.0 mm, REF 5-22516 f) 8.5 mm, REF 5-22517 g) 9.0 mm, REF 5-22518 h) 6.0 mm, REF 5-22512 i) 6.5 mm, REF 5-22513 Product Usage: Tracheal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2461-2019·2019-09-18

    Allergan Recalls Textured Breast Implants Due to Lymphoma Risk

    Allergan is recalling 4 million textured breast implants and tissue expanders worldwide due to an increased risk of anaplastic large cell lymphoma.

    Product
    Natrelle 510, TruForm, Dual-Gel, BIOCELL, Styles LX, MX, FX Product Usage: Breast augmentation and Breast reconstruction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2318-2019·2019-09-18

    Teleflex Recalls Sheridan/HVT Novaplus Tracheal Tubes Due to Disconnection Risk

    Teleflex Medical is recalling specific lots of Sheridan/HVT Novaplus tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.

    Product
    Sheridan/HVT Novaplus: a) 7.0 mm, REF V5-10314 b) 7.5 mm, REF V5-10315 c) 8.0 mm, REF V5-10316 d) 8.5 mm, REF V5-10317 Product Usage: Tracheal tube/airway management
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V665000·2019-09-18

    Mercedes-Benz and Freightliner Sprinter Recalled for Hood Latch Defect

    Daimler Vans USA is recalling 2018-2019 Sprinter vans because an improperly tightened hood screw may allow the hood to open while driving, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2316-2019·2019-09-18

    Teleflex Medical Recalls Hudson RCI Sheridan/HVT Tracheal Tubes

    Teleflex Medical is recalling specific lots of Hudson RCI Sheridan/HVT tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF 5-10312 d) 6.5 mm, REF 5-10313 e) 7.0 mm, REF 5-10314 f) 7.5 mm, REF 5-10315 g) 8.0 mm, REF 5-10316 h) 8.5 mm, REF 5-10317 i) 9.0 mm, REF 5-10318 j) 10.0 mm, REF 5-10320 Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2454-2019·2019-09-18

    Allergan Recalls Textured Breast Implants Due to Lymphoma Risk

    Allergan PLC is recalling specific textured breast implants and tissue expanders due to a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).

    Product
    Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate Profile, Sterile, for the following style numbers: Style 110:110-090, 110-120, 110-150, 110-180, 110-210, 110-240, 110-270, 110-300, 110-330, 110-360, 110-390, 110-420, 110-450, 110-480…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2312-2019·2019-09-18

    Teleflex Medical Recalls Hudson RCI Sheridan/CF Tracheal Tubes

    Teleflex Medical is recalling Hudson RCI Sheridan/CF tracheal tubes because specific lots of the 15 mm Sheridan connector may disconnect from the endotracheal tube, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan/CF: a) 3.0 mm, REF 5-10106, REF 5-10206 b) 3.5 mm, REF 5-10107 c) 4.0 mm, REF 5-10108, REF 5-10208 d) 4.5 mm, REF 5-10109 e) 5.0 mm, REF 5-10110, REF 5-10210 f) 5.5 mm, REF 5-10111 g) 6.0 mm, REF 5-10112, REF 5-10212 h) 6.5 mm, REF 5-10113, REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2458-2019·2019-09-18

    Allergan Recalls McGhan Tissue Expanders Due to Lymphoma Risk

    Allergan is recalling McGhan Croissant-Shaped Tissue Expanders because the FDA identified a higher incidence of anaplastic large cell lymphoma in patients with textured breast implants.

    Product
    McGhan Croissant-Shaped Tissue Expanders, Style 134 Product Usage: intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2126-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Plastic Contamination

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Chocolate Coconut Item Code CS812067, UPC Code 20203-5, UPC GTIN 10787325202032. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2494-2019·2019-09-18

    Zeus Scientific Recalls Dynex DSX Software for False Negative ELISA Results

    Zeus Scientific is recalling 28 Dynex DSX software files due to a programming error that causes false negative results in specific ELISA assays.

    Product
    Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay File Software: ZEUS vl B. burgdorferi lgG-lgM.asy ZEUS vl Borrelia VlsEl-pepClO lgG-lgM.asy ZEUS Parvovirus B19 lgG (9Z7701G).asy ZEUS Parvovirus B19 lgM (9Z7701M).asy ZEUS vl HSV-1 and 2 lgM.asy ZEUS vl…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2125-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and Cookie Dough Ice Cream Bites due to potential free-floating foreign plastic pieces.

    Product
    Bubbies Mochi Ice Cream -Blood Orange Item Code CS800490, UPC Code 20085-7, UPC GTIN 10787325200854. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2143-2019·2019-09-18

    Bubbies and Trader Joe's Mochi Ice Cream Recalled for Plastic Pieces

    Bubbies and Trader Joe's are recalling specific mochi ice cream products due to the potential for free-floating foreign plastic pieces.

    Product
    Trader Joes - Green Tea Item Code 64669, UPC Code 00645003. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2139-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Plastic Contamination

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Vanilla Item Code CS800002, UPC Code 20013-0, UPC GTIN 10787325200137 Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2138-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and Cookie Dough Ice Cream Bites due to potential foreign plastic pieces.

    Product
    Bubbies Mochi Ice Cream -Triple Chocolate Item Code CS800012, UPC Code 20084-0, UPC GTIN 10787325200847 Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2128-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces.

    Product
    Bubbies Mochi Ice Cream -Chocolate Mint Item Code CS812083, UPC Code 20103-8, UPC GTIN 10787325201035. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2539-2019·2019-09-18

    Stryker Recalls Berchtold Chromophare F528 Surgical Lights Due to Assembly Defect

    Stryker is recalling 946 Berchtold Chromophare F528 surgical lights because the back cover of the light head was insufficiently assembled and could fall off.

    Product
    Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment rooms. They provide localized lighting focused on the patient s body for detecting and treating disease, injury, and disability. The surgical lights may only…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2540-2019·2019-09-18

    Stryker Recalls Berchtold Chromophare F628 Surgical Lights Due to Assembly Defect

    Stryker is recalling 3,344 Berchtold Chromophare F628 surgical lights because the back cover of the light head was insufficiently assembled and could fall off.

    Product
    Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment rooms. They provide localized lighting focused on the patient s body for detecting and treating disease, injury, and disability. The surgical lights may only…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2496-2019·2019-09-18

    Aesculap Caiman Disposable Surgical Instruments Recalled for Sterility Concerns

    Aesculap Implant Systems LLC is recalling Caiman disposable articulated instruments due to a possibility of insufficient sterilization.

    Product
    CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2131-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and related products due to potential foreign plastic pieces. The recall covers 3.4 million cases distributed nationwide and internationally.

    Product
    Bubbies Mochi Ice Cream -Li Hing Mango Item Code CS800237, UPC Code 20333-9, UPC GTIN 10787325203336. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2135-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Pistachio Item Code CS800054, UPC Code 20113-7, UPC GTIN 10787325201134. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2140-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces.

    Product
    Bubbies Mochi Ice Cream Premium Variety Pack (Strawberry, Green Tea, Mango) Item Code CS1600001, UPC Code 40013-4, UPC GTIN 10787325400131 Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2132-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -lychee Item Code CS800001, UPC Code 20033-8, UPC GTIN 10787325200335. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2134-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Passion Fruit Item Code CS800119, UPC Code 20093-2, UPC GTIN 10787325200939. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V666000·2019-09-18

    Mercedes-Benz Recalls 2019 Metris Vehicles Due to Head Restraint Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vehicles because head restraint spring pins may be missing or improperly mounted, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide