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.

57076–57100 of 76887

  • ModerateFDA (Food)·F-1675-2015·2015-04-08

    Health One Recalls Siberian Ginseng Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling 199 units of Siberian Ginseng supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Siberian Ginseng, 100 capsules, 500 mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1339-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 153 Freedomaire Surgical Helmets because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET WITH MOTOR MODULE, REF 11113STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1636-2015·2015-04-08

    Health One Pharmaceuticals Recalls Bone Essense Dietary Supplement

    Health One Pharmaceuticals is recalling Bone Essense, 60 capsules, due to significant violations of cGMP regulations for dietary supplements.

    Product
    Bone Essense, 60 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1749-2015·2015-04-08

    Health One Pharmaceuticals Recalls Protein Powder for cGMP Violations

    Health One Pharmaceuticals is recalling Protein Powder due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

    Product
    Protein Powder
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1767-2015·2015-04-08

    Health One Pharmaceuticals Recalls U O Clear Dietary Supplements

    Health One Pharmaceuticals is recalling U O Clear dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    U O Clear
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1344-2015·2015-04-08

    Microtek Medical Recalls Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling non-sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), REF 24009, QTY 24\CS, NON-STERILE Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1768-2015·2015-04-08

    Health One Pharmaceuticals Recalls Ultra Lecithin Dietary Supplements

    Health One Pharmaceuticals is recalling Ultra Lecithin dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Ultra Lecithin
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1365-2015·2015-04-08

    Medtronic Recalls Trellis 6 and 8 Peripheral Infusion Systems for Sterility Breach

    Medtronic is voluntarily recalling Trellis 6 and 8 Peripheral Infusion Systems due to potential sterility breaches in the outer packaging.

    Product
    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1706-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cardiospecs Dietary Supplements

    Health One Pharmaceuticals is recalling Cardiospecs dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Cardiospecs
    Category
    Food
    Distribution
    Distributed nationwide