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.

44201–44225 of 76863

  • CriticalFDA (Food)·F-2439-2017·2017-07-12

    Bulletproof Vanilla Shortbread Collagen Protein Bar Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Vanilla Shortbread Collagen Protein Bars due to potential Listeria monocytogenes contamination. The recall covers specific lots distributed nationwide and internationally.

    Product
    Vanilla Shortbread Collagen Protein Bar. Each Bar is packed in foil wrapper, net wt. per Bar is 1.58 oz (45g). There 12 bars packed in a box and the net wt. is 18.96 oz (540g). Individual Bar UPC 815709021481. Box UPC 815709020804.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2438-2017·2017-07-12

    Bulletproof Lemon Cookie Collagen Protein Bar Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Lemon Cookie Collagen Protein Bars due to potential Listeria monocytogenes contamination. The recall covers specific lots sold nationwide and internationally.

    Product
    Lemon Cookie Collagen Protein Bar. Each Bar is packed in foil wrapper, net wt. per Bar is 1.58 oz (45g). There 12 bars packed in a box and the net wt. is 18.96 oz (540g). Individual Bar UPC 815709021801. Box UPC 815709021795.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2440-2017·2017-07-12

    Bulletproof Recalls Vanilla Shortbread Collagen Protein Bites for Listeria Risk

    Bulletproof 360 Inc is recalling Vanilla Shortbread Collagen Protein Bites due to potential Listeria monocytogenes contamination. The recall covers specific lots distributed nationwide and internationally.

    Product
    Vanilla Shortbread Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bar is 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021504. Box UPC 815709021511.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0940-2017·2017-07-12

    Alvogen Recalls Clindamycin Injection Vials Due to Sterility Concerns

    Alvogen, Inc. is recalling 72,575 vials of Clindamycin Injection USP due to a lack of assurance of sterility. The affected lots were distributed nationwide.

    Product
    Clindamycin Injection USP; 600 mg/4 mL (150 mg/mL). 4 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-463-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0946-2017·2017-07-12

    Fagron Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns

    Fagron Compounding Services is voluntarily recalling 1,056 syringes of Succinylcholine Chloride because the company cannot ensure the product is sterile.

    Product
    Succinylcholine Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N. Wichita, KS 67226 UPC 7335968405
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0941-2017·2017-07-12

    Alvogen Recalls Clindamycin Injection Vials Due to Sterility Concerns

    Alvogen, Inc. is recalling specific lots of Clindamycin Injection USP due to a lack of assurance of sterility. The recall covers 71,825 vials distributed nationwide.

    Product
    Clindamycin Injection USP; 900 mg/6 mL (150 mg/mL). 6 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-464-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0949-2017·2017-07-12

    Phillips Recalls Diabecline Topical Ointment Due to Manufacturing Deviations

    Phillips Co. is recalling Diabecline brand Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that question the product's safety and quality.

    Product
    Diabecline brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-100-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2437-2017·2017-07-12

    Bulletproof Fudge Brownie Collagen Protein Bites Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Fudge Brownie Collagen Protein Bites due to potential Listeria monocytogenes contamination. The recall covers products sold nationwide and internationally.

    Product
    Fudge Brownie Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bite 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021528. Box UPC 815709021535.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0952-2017·2017-07-12

    Phillips Co. Recalls VenomX Zinc Acetate Skin Protectant Due to GMP Deviations

    Phillips Co. is recalling VenomX Zinc Acetate Skin Protectant because FDA inspections found manufacturing practices that question the product's safety and quality.

    Product
    VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2657-2017·2017-07-12

    CardioTek EP-TRACER Software Recalled for Unintentional Parameter Changes

    CardioTek BV is recalling EP-TRACER Software V1.x and V2.0 due to a bug that allows parameters to be changed unintentionally during use.

    Product
    CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is an electrophysiology measurement system used to acquire, filter, digitize, amplify, display, and record signals obtained during electrophysiological studies and related procedures. The system allows the user…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2436-2017·2017-07-12

    Bulletproof Fudge Brownie Collagen Protein Bar Recalled for Listeria Risk

    Bulletproof 360 Inc is recalling Fudge Brownie Collagen Protein Bars due to potential Listeria monocytogenes contamination.

    Product
    Fudge Brownie Collagen Protein Bar. Each bar is packed in foil wrapper, net wt. per bar 1.58 oz (45g). There 12 bars packed in a box and the net wt. per box is 18.96 oz (540g). Individual Bar UPC 815709021498. Box UPC 815709020811.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0951-2017·2017-07-12

    Phillips Recalls StaphWash Skin Protectant Due to Manufacturing Deviations

    Phillips Co. is recalling StaphWash+Plus+ Skin Protectant because FDA inspections found manufacturing practices that question the product's safety and quality.

    Product
    StaphWash+Plus+ Skin Protectant, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 43074-101-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0939-2017·2017-07-12

    Alvogen Recalls Clindamycin Injection Vials Due to Sterility Concerns

    Alvogen, Inc. is recalling 5,100 vials of Clindamycin Injection USP due to a lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Clindamycin Injection USP; 300 mg/2 mL (150 mg/mL). 2 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-462-69
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0947-2017·2017-07-12

    Phillips Tetracycline Ointment Recalled for Manufacturing Quality Concerns

    Phillips Co. is recalling Tetracycline-ABC Brand Topical Ointment because FDA inspections found significant manufacturing deviations that raise questions about product safety and quality.

    Product
    Tetracycline-ABC Brand Topical ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 4307410201
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0948-2017·2017-07-12

    TetraStem Topical Antibiotic Ointment Recalled for Manufacturing Deviations

    Phillips Co. is recalling TetraStem Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that raise questions about product safety and quality.

    Product
    TetraStem brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-301-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0950-2017·2017-07-12

    Phillips Co. Recalls StingMed Insect Bites Skin Protectant Due to GMP Deviations

    Phillips Co. is recalling StingMed Insect Bites Skin Protectant because FDA inspections found significant manufacturing deviations that raise questions about the product's safety and quality.

    Product
    StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 04307-100-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2446-2017·2017-07-12

    Atlantic Gold Battered Mushrooms Recalled for Undeclared Milk Allergen

    Oxford Frozen Foods is recalling Atlantic Gold Battered Mushrooms because the product may contain undeclared milk, a major food allergen.

    Product
    Small White Button Mushroom Regular Batter: ATLANTIC GOLD Battered Mushrooms Net Weight 5 lb (2.27 kg) - 34086; Atlantic Gold Battered Mushrooms 6 x 2 lbs 12 lbs - 34112;
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-2442-2017·2017-07-12

    Atlantic Gold Battered Onion Rings Recalled for Undeclared Milk

    Oxford Frozen Foods is recalling Atlantic Gold Battered Onion Rings because the product may contain undeclared milk.

    Product
    33034 33116 Thick Cut Regular Batter: ATLANTIC GOLD STEAK CUT BATTERED ONION RINGS NET WT 10 lb (4.54 kg) - 33166
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2667-2017·2017-07-12

    Exactech Equinoxe Reamer Recalled for Updated Instructions on Glenoid Reaming

    Exactech is recalling the Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer to update instructions for use, clarifying proper reaming technique to prevent instrument breakage.

    Product
    EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer Catalog #: 321-45-01
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Food)·F-2414-2017·2017-07-12

    GoMacro Recalls Specific Thrive Bars Due to Listeria Risk

    GoMacro is recalling specific THRIVE Chocolate, Nuts & Sea Salt bars because they may be contaminated with Listeria monocytogenes.

    Product
    go macro THRIVE Chocolate, Nuts & Sea Salt bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00650 4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2443-2017·2017-07-12

    Oxford Frozen Foods Recalls Ale House Onion Rings for Undeclared Milk

    Oxford Frozen Foods is recalling Ale House Beer Battered Onion Rings because the product may contain undeclared milk. This poses a risk to consumers with milk allergies.

    Product
    ALE HOUSE BEER BATTERED 3/8 ONION RINGS - NET WT. 4/2.5 lb (1.13 kg) 10 lb (4.54 kg) - 33221
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-2413-2017·2017-07-12

    GoMacro Recalls Specific MacroBars and Thrive Bars Due to Listeria Risk

    GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.

    Product
    go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar, UPC 8 53555-00671 9 and 2. net Wt 2.3 oz / 65 G, UPC 8 53555-00668 9
    Category
    Food
    Distribution
    Distributed nationwide