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.

57051–57075 of 76887

  • ModerateFDA (Food)·F-1660-2015·2015-04-08

    Health One Pharmaceuticals Recalls Herbal Health Dietary Supplements

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

    Product
    Herbal Health
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1358-2015·2015-04-08

    Bard Urinary Drainage Bags Recalled for Potential Sterile Barrier Breach

    C.R. Bard is recalling specific lots of urinary drainage bags due to a potential breach of the sterile barrier packaging.

    Product
    Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot # NGYJ0603 and NGYJ1671
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2015·2015-04-08

    Microtek Medical recalls sterile smoke evacuator wands due to latex packaging

    Microtek Medical is recalling sterile smoke evacuator wands because the packaging contains latex but lacks the required warning label.

    Product
    INTEGRAL WAND W/TUBING, STERILE, REF 24185, QTY 24/CS, STERILE EO 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, Trauma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1352-2015·2015-04-08

    Synthes Aiming Arms Recalled Due to Potential Jamming of Guide Sleeve

    Synthes, Inc. is recalling 131 Aiming Arms from the TFN-ADVANCED system because the guide sleeve may jam, potentially delaying instrument removal.

    Product
    Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part of the TFN-ADVANCED (TFNA) System. The TFN-ADVANCED Proximal Femoral Nailing System is intended for treatment of fractures in adults and adolescents (12-21)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1676-2015·2015-04-08

    Health One Pharmaceuticals Recalls Reishi Spore Gen Dietary Supplements

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

    Product
    Reishi Spore Gen, 90 Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1340-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 11 units of Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH BELT, REF 11114STK, 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 (Devices)·Z-1367-2015·2015-04-08

    Nidek YC-1800 Ophthalmic YAG Laser System Recalled for Pitting Lens

    Nidek Inc is recalling 799 YC-1800 Ophthalmic YAG Laser Systems due to complaints of pitting lenses that may cause unclear images.

    Product
    YC-1800 OPHTHALMIC YAG LASER SYSTEM; The YC-1800 allows the safe and bloodless treatment of intraocular diseases for outpatients by mechanical disruption caused by energy of the YAG laser pulses.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1764-2015·2015-04-08

    Health One Pharmaceuticals Recalls Super pill#2 Dietary Supplements

    Health One Pharmaceuticals is recalling Super pill#2 dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Super pill#2
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1708-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cholesterol Formula Due to cGMP Violations

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

    Product
    Cholesterol Formula, 90 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1345-2015·2015-04-08

    Microtek Medical Recalls Sterile Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling 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), WITH TUBING EXTENDER, STERILE, REF 24010, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures.…
    Category
    Medical Device
    Distribution
    Distributed nationwide