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.

57626–57650 of 76887

  • SevereFDA (Devices)·Z-1018-2015·2015-02-11

    FDA Recalls Covidien Trellis-8 Peripheral Infusion Systems Due to Labeling Error

    FDA is recalling 1,032 units of the Covidien Trellis-8 Peripheral Infusion System because a manufacturing error caused the proximal and distal balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT812025. The following models are not offered for sale in the US: EVT808015, EVT808025, EVT812015, and EVT812025 Sterile EO. Product Usage: Intended for controlled and selective…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0957-2015·2015-02-11

    Reily Foods Recalls White Chicken Chili Kits Due to Undeclared Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand White Chicken Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT, 3 oz. (85 g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-72396-10019-0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0959-2015·2015-02-11

    Reily Foods Recalls Wick Fowler's Chili Kits for Undeclared Allergens

    Reily Foods is recalling Wick Fowler's Texas Style False Alarm Mild Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit, NET WT. 3.03 oz. (86g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-71092-00111-4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0382-2015·2015-02-11

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 120,900 vials of 1% Lidocaine Hydrochloride Injection because iron oxide particulates were found in the solution.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2015·2015-02-11

    Invacare Recalls G-Series Bed Rails Due to Entrapment Safety Defect

    Invacare is recalling G-Series bed rails because the mounting bracket does not meet entrapment safety specifications.

    Product
    G- Series Beds; G29 full length bed rails assembly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1042-2015·2015-02-11

    Zimmer Persona Tibial Inserter Recalled for Potential Tip Fracture

    Zimmer, Inc. is recalling 1,091 Persona Tibial Articular Surface Inserters due to a potential fracture of the instrument tip, which could cause tissue damage or require revision surgery.

    Product
    Zimmer PERSONA Tibial Articular Surface Inserter; Item # 42-5299-001-00. Manual surgical instrument for knee arthroplasty (orthopedic).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15077·2015-02-11

    System Sensor Recalls Combination Carbon Monoxide and Smoke Detectors

    System Sensor is recalling i4 Series combination CO/smoke detectors because they may fail to detect carbon monoxide, posing a poisoning risk.

    Product
    i4 Series System Sensor combination carbon monoxide (CO)/smoke detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2015·2015-02-11

    SCC Soft Computer Recalls SoftLab Laboratory Information System Versions

    SCC Soft Computer is recalling SoftLab versions 4.0.7.0 and 4.0.7.1 because the software fails to send abnormal flags for Reference Lab test results.

    Product
    SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory information system to be used in a medical research or clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0972-2015·2015-02-11

    Zilks Foods Recalls Green Chili Hummus Due to Undeclared Peanuts

    Zilks Foods is recalling 3,176 cups of Green Chili Hummus because the cumin ingredient may contain undeclared peanuts.

    Product
    Hummus; All-natural ZILKS HATCH GREEN CHILI HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0971-2015·2015-02-11

    Zilks Foods Recalls Balsamic and Garlic Hummus for Undeclared Peanuts

    Zilks Foods is recalling 2,424 cups of Balsamic and Garlic Hummus due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS BALSAMIC & GARLIC HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0973-2015·2015-02-11

    Zilks Spinach and Artichoke Hummus Recalled for Undeclared Peanuts

    Zilks Foods is recalling Spinach & Artichoke Hummus because the cumin ingredient may contain undeclared peanuts.

    Product
    Hummus; All-natural ZILKS SPINACH & ARTICHOKE HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1049-2015·2015-02-11

    Carl Zeiss Meditec FORUM Archive and Viewer Software Recall

    Carl Zeiss Meditec is recalling FORUM Archive and Viewer software versions 3.1 and 3.2 due to a defect that may lead to misinterpretation of optical coherence tomography data.

    Product
    FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catalog numbers: 000000-20107-750 (DVD with either FORUM v 3.1 or v 3.1.1) 000000-2058-601 (DVD with either FORUM v 3.2 or 3.2.1); 000000-2084-928 (USB drive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1039-2015·2015-02-11

    Baxter Integrated APD Set Recalled for Leakage Complaints

    Baxter Healthcare is recalling 8,640 units of Integrated APD Sets with Cassette 3-Prong due to leakage complaints. The sterile fluid path is used for peritoneal dialysis.

    Product
    Baxter Integrated APD Set with Cassette 3-Prong, Sterile, nonpyrogenic fluid path. Product Usage: The recall device is indicated for use in the treatment of patients with renal failure to provide PD fluid exchanges with Baxter HomeChoice PD Systems in clinical and home use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1040-2015·2015-02-11

    Sedecal MobileDiagnost wDR X-ray systems recalled for unexpected movement

    Sedecal S.A. is recalling 283 MobileDiagnost wDR motorized portable diagnostic X-ray systems due to reports of unexpected movement.

    Product
    MobileDiagnost wDR motorized portable diagnostic X-ray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0969-2015·2015-02-11

    Zilks Roasted Red Pepper Hummus Recalled for Undeclared Peanuts

    Zilks Foods is recalling 4,008 cups of Roasted Red Pepper Hummus due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS ROASTED RED PEPPER HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1055-2015·2015-02-11

    BD 10 mL Syringes Recalled Due to Improperly Seated Stopper

    Becton Dickinson is recalling 564,000 units of 10 mL syringes because the stopper is not properly seated in the syringe.

    Product
    BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula, Not for Skin Injection ; Catalog #303348, BD 10 mL Syringe Luer-Lok Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40 mm), not for skin injection; Catalog #305064 BD 10 mL Syringe Luer-Lok Tip with BD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0968-2015·2015-02-11

    Zilks Hummus Recalled for Potential Undeclared Peanuts

    Zilks Foods is recalling 4,768 cups of hummus nationwide due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS FAMOUS ORIGINAL HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1052-2015·2015-02-11

    Zimmer Recalls Persona Tibial Articular Surface Provisional Shims Due to Cleaning Defect

    Zimmer, Inc. is recalling Persona Tibial Articular Surface Provisional Shims because repeated sonic cleaning can break the ball bearing retention feature, potentially leaving parts in the surgical wound.

    Product
    Persona (TASP) Tibial Articular Surface Provisional Shim, all sizes and Lots Catalog Number: 42-5279-002-00 thru 42-5279-009-04. Product Usage: The Persona TASPs are sterilizable instruments Intended for multiple uses. The TASP components are used to aid the surgeon in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1041-2015·2015-02-11

    Roche Cobas b 221 Blood Gas Analyzer Recalled for Measurement Bias

    Roche Diagnostics is recalling 103 Cobas b 221 analyzers because bacterial contamination causes inaccurate glucose and lactate readings.

    Product
    Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0974-2015·2015-02-11

    Zilks Hummus with Real Bacon Recalled for Potential Undeclared Peanuts

    Zilks Foods is recalling 3,808 cups of hummus with real bacon due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS HUMMUS with REAL BACON GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1053-2015·2015-02-11

    CareFusion Recalls SmartSite Infusion Sets Due to Disconnection and Leakage

    CareFusion is recalling 7,440 SmartSite Low Sorbing Infusion Sets due to disconnection and leakage issues.

    Product
    SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein. The set is comprised of components commonly found on intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide