The Recall Desk

State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46276–46300 of 76871

  • HighFDA (Devices)·Z-1205-2017·2017-02-22

    Atrium Medical Recalls Maquet Ocean Water Seal Chest Drains

    Atrium Medical is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after being depressed.

    Product
    Maquet Ocean Water Seal Chest Drain, Single Collection WAC Reference: 2002-000 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2017·2017-02-22

    Atrium Medical Recalls Maquet Oasis Chest Drains Due to Valve Defect

    Atrium Medical is recalling Maquet Oasis chest drains because the manual vent valve may fail to re-seal after use.

    Product
    Maquet Oasis Dry Suction Water Seal Chest Drain, Single Collection w/AC Reference: 3600-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1211-2017·2017-02-22

    Atrium Medical Recalls Maquet Express Dry Seal Suction OASIS Drain

    Atrium Medical Corporation is recalling 18 units of Maquet Express Dry Seal Suction OASIS Drain because the manual vent valve may fail to re-seal.

    Product
    Maquet Express Dry Seal Suction OASIS DRAIN, DRY PEDI W/AC Reference: 3612-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1208-2017·2017-02-22

    Atrium Medical Recalls Maquet Express Dry Seal Suction Chest Drains

    Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction Chest Drains because the manual vent valve may fail to re-seal after being depressed.

    Product
    Maquet Express Dry Seal Suction Chest Drain, Single Collection w/AC Reference: 4000-100N Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1480-2017·2017-02-22

    Joe Chips Potato Chips Recalled for Potential Salmonella Contamination

    The Two Little Guys Company is recalling Joe Chips Sour Cream & Toasted Onion potato chips because a milk powder ingredient may be contaminated with Salmonella.

    Product
    Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Distributed by: The Joe Tea Company, Upper Montclair, NJ 07043-0255 (973)744-7502 Net Wt. 2 OZ UPC 743234001725 Net Wt. 5 OZ UPC 743234001800
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0474-2017·2017-02-22

    Aurobindo Recalls Venlafaxine Hydrochloride Capsules Due to Physical Defects

    Aurobindo Pharma USA Inc is recalling 47,040 bottles of Venlafaxine Hydrochloride extended-release capsules because some contain punctured or clumped capsules.

    Product
    VENLAFAXINE HYDROCHLORIDE — VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1222-2017·2017-02-22

    Atrium Thoracic Catheter Recall Due to Incorrect Labeling Icon

    Atrium Medical Corporation is recalling 1,394 cases of 10 Fr Straight Thoracic Catheters because the label icon incorrectly depicts six eyelets instead of two.

    Product
    Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0476-2017·2017-02-22

    Actavis Recalls Glipizide Extended-Release Tablets Due to Dissolution Failure

    Actavis Inc is recalling specific lots of Glipizide extended-release tablets because they failed to meet dissolution specifications at the 10-hour testing point.

    Product
    Glipizide extended-release tablets, 2.5mg, 30-count bottle, Rx Only, Manufactured By Patheon Pharmaceuticals Inc Cincinnati OH 45237 USA, NDC 0591-0900-30, UPC 3-0591090030-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1204-2017·2017-02-22

    Siemens CentraLink Software Recalled for Potential Sample Type Omission

    Siemens is recalling CentraLink Data Management System software versions v13x, v14x, and v15x because the system may download orders to the ADVIA Automation System without specifying the sample type.

    Product
    CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network solution provider and multi-system data manager for the instruments and lab automation systems (LAS) within the lab. The CentraLink software consolidates data from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2017·2017-02-22

    BD Vacutainer Blood Collection Tubes Recalled for Excess Anticoagulant

    Becton Dickinson is recalling specific lots of BD Vacutainer blood collection tubes because they contain approximately twice the expected amount of buffered sodium citrate additive.

    Product
    BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5 ml x 13 x 75 mm) Catalog Number: 369714 Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection tube that provides means of collecting, transporting and processing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0479-2017·2017-02-22

    Teva Recalls Mimvey Lo Tablets Due to Impurity Test Failures

    Teva Pharmaceuticals USA is recalling specific lots of Mimvey Lo tablets because they failed impurity specifications for norethindrone.

    Product
    Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1190-2017·2017-02-22

    Greatbatch Recalls T5766 Offset Reamer Handles Due to Drive Chain Seizure

    Greatbatch Medical is recalling 1,441 T5766 Offset Reamer Handles because the drive chain U-joints may seize during hip surgery, rendering the device non-functional.

    Product
    Offset Reamer Handle, T5766 Product Usage: The reamer handles are re-usable surgical instruments used in arthroplasty surgery of the hip joints, where either total joint replacement or resurfacing surgery is performed using a reamer cutting instrument. The reamer handles are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1221-2017·2017-02-22

    Atrium Medical Recalls 8 Fr Thoracic Catheters Due to Labeling Error

    Atrium Medical Corporation is recalling 8 Fr Straight Thoracic Catheters because the label depicts six eyelets instead of the correct two.

    Product
    Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0478-2017·2017-02-22

    Accord Healthcare Recalls Lisinopril Tablets Due to Missing Break Line

    Accord Healthcare is recalling 12,896 bottles of 5 mg Lisinopril tablets because the tablets are missing a break line. The recall covers the U.S. and Puerto Rico.

    Product
    Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-376-17
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1196-2017·2017-02-22

    Argon Medical Devices Recalls Harvest Needles Due to Sterility Concerns

    Argon Medical Devices is recalling 15 boxes of Harvest Needles because a potential defect in the blister packaging may compromise the sterility of the product.

    Product
    HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0477-2017·2017-02-22

    Taclonex Topical Suspension Recalled for Outdated Package Insert

    LEO Pharma Inc. is recalling Taclonex topical suspension because it was packaged with an out-of-date package insert.

    Product
    TACLONEX — TACLONEX (CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1484-2017·2017-02-22

    NOW Foods Recalls Multi-Food 1 Tablets Due to Labeling Error

    NOW Foods is recalling Multi-Food 1 Tablets because the label incorrectly states the molybdenum content is 75 mg instead of 75 mcg.

    Product
    NOW¿ Multi-Food 1 Tablets, One Tablet Daily, 90 tablets, A Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V111000·2017-02-21

    Yamaha Recalls 2015-2016 YZF-R3 Motorcycles for Fuel Tank Leak Risk

    Yamaha is recalling 2015-2016 YZF-R3 motorcycles because engine vibration may cause the fuel tank bracket to contact the tank, potentially leading to a fuel leak and fire risk.

    Product
    YAMAHA — YAMAHA redundant YZF-R3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E012000·2017-02-21

    LiquidSpring Recalls Suspension Systems Due to Brake Bolt Tightening Defect

    LiquidSpring is recalling certain Compressible Liquid Adaptive Suspension Systems because overtightened rear brake banjo bolts may cause loss of rear brakes, increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17090·2017-02-21

    Yamaha Recalls Grand Piano Benches Due to Lead Paint Violation

    Yamaha Corporation of America is recalling about 900 piano benches sold with grand pianos because the interior paint contains excessive lead, violating federal standards.

    Product
    Piano benches sold with Yamaha grand piano
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V108000·2017-02-20

    Winnebago Recalls 2016-2017 Travato RVs Due to Propane Hose Hazard

    Winnebago is recalling 2016-2017 Travato recreational vehicles because the liquid propane hose may contact the emergency brake cable, potentially causing a propane leak that increases the risk of fire or explosion.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E010000·2017-02-20

    Autoliv Recalls AI2 Air Bag Initiators Due to Deployment Failure Risk

    Autoliv is recalling AI2 Air Bag Initiators manufactured between June 2016 and November 2016 because an improper chemical mix may prevent air bags from deploying properly in a crash.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E011000·2017-02-20

    Roush Propane Conversion Kits Recalled for Potential Fuel Leak

    Roush CleanTech is recalling propane conversion kits for Ford F-250 trucks because worn fittings may cause a propane leak, increasing fire risk.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide