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.

Which agencies issued them

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.

57226–57250 of 76887

  • HighFDA (Devices)·Z-1299-2015·2015-03-25

    Fisher Brand Infant Heel Warmers Recalled for Burn Risk

    CooperSurgical is recalling Fisher Brand Gel and Liquid Infant Heel Warmers because products without expiration dates pose a remote potential for minor burns.

    Product
    Fisher Brand Gel Infant Heel Gel Warmers, Cat. No.: 22-024647 Fisher Brand Liquid Infant Heel Warmer, Cat. No: 22-024646 To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1451-2015·2015-03-25

    Goya Black Bean Soup Recalled for Possible Peanut Contamination

    Goya Foods is recalling 29-ounce cans of Black Bean Soup and Kirby brand black beans due to possible peanut contamination.

    Product
    Goya Black Bean Soup Net Wt. 29 oz. Goya Foods, Secaucus, NJ 07096 Product of Dominican Republic UPC 0 4133102081 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V175000·2015-03-25

    Ford Recalls 2011-2015 F-Series Trucks With Emergency Vehicle Packages

    Ford is recalling 6,322 model year 2011-2015 F-350, F-450, and F-550 trucks equipped with ambulance or fire engine packages due to a software defect that may cause the engine to shut down unexpectedly.

    Product
    FORD — FORD F-550 SD, F-450 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1292-2015·2015-03-25

    Baxter HomeChoice Pro APD System Recalled for Occluder Defect

    Baxter Healthcare is recalling 75 HomeChoice Pro APD systems because the occluder may have sharp edges or separate, causing system errors or therapy termination.

    Product
    The HomeChoice Pro APD System is a peritoneal dialysis system. The HomeChoice Pro Automated Personal Cycler peritoneal dialysis system is intended for automatic control of dialysate solution exchange in the treatment of pediatric and adult renal failure patients undergoing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1286-2015·2015-03-25

    Smiths Medical Recalls CADD Medication Cassette Reservoirs Due to Leak Risk

    Smiths Medical is recalling specific lots of 50mL CADD Medication Cassette Reservoirs because they may leak at the sealing area. No serious injuries or deaths have been reported.

    Product
    CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1297-2015·2015-03-25

    Siemens E.CAM Systems Recalled for Incorrectly Assembled Radial Motor Drives

    Siemens Medical Solutions is recalling E.CAM emission computed tomography systems because radial motor drives replaced during service were assembled backwards.

    Product
    E.CAM emission computed tomography system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1301-2015·2015-03-25

    CooperSurgical Recalls NovaPlus Infant Heel Warmers Due to Burn Risk

    CooperSurgical is recalling NovaPlus infant heel warmers because products without expiration dates may cause minor burns.

    Product
    NovaPlus Brand Warm Gel Infant Heel Gel Warmer, Item # V6391 NovaPlus Brand Liquid Heal Warmer. Item #V6393 Single Use and Disposable To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0413-2015·2015-03-25

    Mylan Recalls Subpotent Nicardipine Hydrochloride Injection Vials

    Mylan Institutional LLC is recalling specific lots of Nicardipine Hydrochloride Injection because the product failed potency and impurity specifications.

    Product
    Nicardipine Hydrochloride Injection, 25 mg/10 ml (2.5 mg/mL),10 mL single dose vial, Rx only, Manufactured in India for: Mylan Institutional LLC, Rockford, IL 61103, NDC 67457-224-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0419-2015·2015-03-25

    Tarmac Recalls Antacid Liquid Due to Microbial Contamination

    Tarmac Products is recalling specific lots of Antacid Liquid Regular Strength because they failed microbiological testing at the 12-month time point.

    Product
    Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200 mg, Magnesium hydroxide 200 mg, Simethicone 20 mg (in each 5 mL, 1 teaspoon), Mint flavor, 12 fl oz (355 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0073-02…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1275-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Flush Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain device kits because open seals may compromise product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Groshong Midline Bard MYPICC Kit 4F (Single-Lumen) The syringe is used to pre-flush the catheter prior to placement and may also be used to verify patency post-placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1296-2015·2015-03-25

    Siemens Symbia E SPECT Systems Recalled for Incorrect Radial Motor Assembly

    Siemens Medical Solutions is recalling 419 Symbia E SPECT systems worldwide because radial motor drives were incorrectly assembled backwards during a customer service action.

    Product
    Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1284-2015·2015-03-25

    St Jude Medical Recalls TactiSys Quartz Pack for Configuration Update

    St Jude Medical is recalling 89 TactiSys Quartz Packs because a configuration update is needed to ensure the device appropriately recognizes all TactiCath catheters.

    Product
    TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias that allows visualization of the contact force between TactiCath quartz catheter tip and the heart wall. Product Usage: This device is indicated for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1291-2015·2015-03-25

    Sybron Recalls Pinnacle Cure Sleeves Due to Mislabeling and Cross-Contamination Risk

    Sybron Dental Specialties is recalling 172 units of Pinnacle Cure Sleeves because inner packaging is mislabeled, creating a risk of cross-contamination if the sleeves tear.

    Product
    Outer cardboard box labeling: Pinnacle Cure Sleeve, Curing Light Tip Sleeves. Kerr Total Care. Part Number: 4513C or 4513-1 Single Patient Use Fits 13mm Tips. Pack of 400. Metrex Research, Manufacturer. Inner individual packaging of each sleeve: Cure Sleeve by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0412-2015·2015-03-25

    Mylan Recalls Doxorubicin Vials Due to Potential Mispackaging

    Mylan Institutional LLC is recalling 936 vials of Doxorubicin Hydrochloride Injection because they may have been mispackaged with Ifosfamide Injection.

    Product
    DOXOrubicin Hydrochloride Injection, USP, 200 mg/100 mL (2 mg/mL), For IV Use Only, Sterile, ISOTONIC SOLUTION, Caution: Cytotoxic Agent, 100 mL Multi-Dose Vial, Rx Only, Manufactured By: Onco Therapies Limited, Bangalore, 560105, INDIA, Distributed By: Amneal-Agila, LLC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V172000·2015-03-24

    Ford Recalls 2013-2015 Lincoln MKT Vehicles Due to Fire Risk

    Ford is recalling specific 2013-2015 Lincoln MKT vehicles with limousine or hearse packages because a vacuum pump relay may overheat, increasing the risk of a vehicle fire.

    Product
    LINCOLN — LINCOLN MKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V170000·2015-03-24

    Spartan Recalls 2011-2016 School Bus Chassis Due to Fire Risk

    Spartan Motors is recalling 2011-2016 school bus chassis because fuel system components may melt, causing engine stalls or vehicle fires.

    Product
    SPARTAN — SPARTAN SB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V171000·2015-03-24

    Ford Recalls 2011-2013 Explorers for Door Handle Spring Defect

    Ford is recalling 2011-2013 Explorers because an interior door handle spring may unseat, preventing the handle from returning to its stowed position. This could cause the door to unlatch in a side impact crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V173000·2015-03-24

    KZ-RV Recalls 723 Recreational Vehicles Due to Failing Entry Step Rivets

    KZ-RV is recalling 723 recreational vehicles because a rivet on the quad entry steps may shear and fail, causing the steps to give and increasing the risk of personal injury.

    Product
    KZ-RV — KZ-RV STONERIDGE, GOLDRUSH DISCOVERY, GOLDRUSH, GOLDRUSH NUGGET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V165000·2015-03-23

    Navistar Recalls 2015-2016 International Trucks Due to Brake Fire Risk

    Navistar is recalling 2015-2016 International and IC Bus vehicles because defective brake actuators may cause dragging, overheating, and wheel end fires.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TRANSTAR, CE, DURASTAR, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V168000·2015-03-23

    Navistar Recalls 2015 IC RE Transit Buses for Brake Hose Defect

    Navistar is recalling 2015 IC RE non-school Transit Buses because the front air brake hose may contact the tire, causing leaks and increased crash risk.

    Product
    IC BUS — IC BUS RECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V166000·2015-03-23

    Navistar Recalls 2015-2016 IC School Buses for Brake Fire Risk

    Navistar is recalling specific 2015-2016 IC school buses because defective air brake actuators may cause dragging brakes and wheel end fires.

    Product
    IC BUS — IC BUS CASB, CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V164000·2015-03-23

    GM Recalls 2013-2015 Chevrolet Malibu for Sunroof Pinch Hazard

    General Motors is recalling 2013-2015 Chevrolet Malibus because the sunroof switch may be pressed inadvertently, causing the roof to close unexpectedly and risk pinch injuries.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide