The Recall Desk

State

Rhode Island product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41976–42000 of 76863

  • LowFDA (Drugs)·D-0131-2018·2018-01-03

    Pharmedium Recalls Morphine Sulfate Injection Due to Labeling Errors

    Pharmedium Services LLC is recalling specific lots of compounded morphine sulfate injection because the labels may have incorrect or missing lot and expiration dates.

    Product
    morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-455-78
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0133-2018·2018-01-03

    Auryxia Ferric Citrate Tablets Recalled for Damaged Desiccant Packets

    Keryx Biopharmaceuticals is recalling Auryxia (ferric citrate) tablets because damaged silica gel packets may allow desiccant granules to contact the medication.

    Product
    AURYXIA — AURYXIA (FERRIC CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18E003000·2018-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2009 Vehicles

    Takata is recalling specific 2009 model year air bag inflators that may explode due to propellant degradation. This affects vehicles registered in 22 specific states.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18E002000·2018-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2010 Vehicles

    Takata is recalling specific frontal passenger air bag inflators in 2010 vehicles registered in 22 states and D.C. due to a risk of explosion causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V002000·2018-01-02

    Forest River Recalls 2018 Surveyor Trailers Due to Fire Risk

    Forest River is recalling 2018 Surveyor recreational trailers because an incorrect circuit breaker can cause wiring to melt, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E001000·2018-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2013 Vehicles

    Takata is recalling specific 2013 model year air bag inflators in 13 states and territories due to a risk of explosion from propellant degradation.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18076·2018-01-02

    Comfort Research Recalls Ultra Lounge Bean Bag Chair Covers

    Comfort Research is recalling about 1,200 Ultra Lounge bean bag chair covers due to risks of entrapment and suffocation to children.

    Product
    Ultra Lounge bean bag chair covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V001000·2018-01-02

    Erwin Hymer Recalls Motorhomes With Defective Fire Extinguishers

    Erwin Hymer is recalling 2012-2018 motorhomes because the installed fire extinguishers may clog and fail to discharge properly.

    Product
    ROADTREK — ROADTREK, HYMER, CARADO ZION, AKTIV, RS ADVENTUROUS, BANFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V847000·2017-12-29

    ShowHauler Recalls 2003-2018 Motorhomes Due to Fire Extinguisher Defect

    ShowHauler is recalling 2003-2018 Garage Coach, Toter Coach, and Motorhome vehicles because their fire extinguishers may clog or detach, posing injury risks during a fire.

    Product
    SHOWHAULER — SHOWHAULER GARAGE COACH, TOTER COACH, MOTORHOME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V846000·2017-12-28

    Forest River Recalls 2017-2018 Georgetown RVs for Brake Defect

    Forest River is recalling 2017-2018 Georgetown recreational vehicles because missing plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18073·2017-12-28

    Western Gas Recalls Propane Due to Fire and Burn Hazards

    Western Gas is recalling under-odorized propane gas due to fire, explosion, and burn hazards. Consumers should contact their supplier for a free inspection.

    Product
    Propane (LP) Gas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0122-2018·2017-12-27

    LaBri's Body Health XPLODE Recalled for Unapproved Sibutramine

    EZWeightLossTX LLC is recalling LaBri's Body Health XPLODE capsules because they contain sibutramine, an unapproved drug ingredient.

    Product
    LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by LaBri's Body Health.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0115-2018·2017-12-27

    Advanced Pharma Recalls Subpotent Nitroglycerin Injection Syringes

    Advanced Pharma Inc. is recalling Nitroglycerin injection syringes found to be subpotent, meaning they contain less active ingredient than labeled.

    Product
    NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (200 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0121-2018·2017-12-27

    FDA Recalls LaBri's Body Health Atomic 60 Capsules for Sibutramine Contamination

    EZWeightLossTX LLC is recalling LaBri's Body Health Atomic 60 Capsules because the product was found to contain sibutramine, an unapproved drug ingredient.

    Product
    LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0123-2018·2017-12-27

    Pfizer Recalls Vancomycin Hydrochloride Vials Due to Glass Particulate Matter

    Pfizer Inc. is recalling 102,500 vials of Vancomycin Hydrochloride for Injection due to the presence of glass particulate matter.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0126-2018·2017-12-27

    FDA Recalls Natural Herbal Coffee AMPT for Undeclared Sildenafil and Tadalafil

    The FDA is recalling Natural Herbal Coffee AMPT because it contains undeclared sildenafil, tadalafil, and milk. The product was marketed without an approved NDA or ANDA.

    Product
    NATURAL HERBAL COFFEE AMPT, sold in 25g packages (UPC 6942630905), 10-count packages per box (UPC 6942630912); Manufactured For: The Ampt Life, LLC.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V844000·2017-12-27

    Thor Motor Coach Recalls 2018 Freedom Traveler Motorhomes for Fire Risk

    Thor Motor Coach is recalling 2018 Freedom Traveler motorhomes because a missing heat shield between the propane tank and generator exhaust pipe increases the risk of fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM TRAVELER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0113-2018·2017-12-27

    Advanced Pharma Recalls Subpotent NitroGlycerin Injection Syringes Nationwide

    Advanced Pharma Inc. is recalling 550 syringes of NitroGlycerin injection found to be subpotent. The product was distributed nationwide to hospitals and medical facilities.

    Product
    NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (100 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0120-2018·2017-12-27

    Amneal Recalls Lorazepam Oral Concentrate Due to Defective Dropper Markings

    Amneal Pharmaceuticals is recalling Lorazepam Oral Concentrate because dropper measurement markings may be reversed, shifted, or missing, which could lead to dosing errors.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0114-2018·2017-12-27

    Advanced Pharma Recalls Subpotent Nitroglycerin Injection Syringes

    Advanced Pharma Inc. is recalling 320 syringes of Nitroglycerin injection that were found to be subpotent, meaning they contain less active ingredient than labeled.

    Product
    NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj, USP QS 5 mL (200 mcg per mL), 5 mL Sterile single dose syringe, packaged in 8 x 5 (FORTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-67.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0128-2018·2017-12-27

    Perrigo Recalls Zephrex-D Nasal Decongestant Due to Microbial Contamination

    L. Perrigo Company is recalling Zephrex-D nasal decongestant softgels due to microbial contamination. Consumers should stop using the product and return it to the pharmacy.

    Product
    Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant. 24 softgel tablets per paper carton, Distributed by Perrigo, Allegan, MI 49010, NDC 70085-151-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0264-2018·2017-12-27

    BioMerieux Recalls ETEST Oxacillin Strips Due to Quality Control Failures

    BioMerieux SA is recalling ETEST Oxacillin strips due to quality control failures that may cause false resistant results.

    Product
    ETEST OXACILLIN OX 256 US F100 In vitro diagnostic, a quantitative technique for determining the antimicrobial susceptibility of bacteria species.
    Category
    Medical Device
    Distribution
    Distributed nationwide