The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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20176–20200 of 39655

  • SevereUSDA FSIS·082-2017·2017-07-15

    Marathon Enterprises Recalls Hot Dogs Due to Bone Fragment Contamination

    Marathon Enterprises is recalling approximately 7.2 million pounds of hot dog products due to potential bone fragment contamination. One minor oral injury has been reported.

    Product
    Marathon Enterprises Inc. — Marathon Enterprises Inc. Recalls Hot Dog Products Due to Possible Extranous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V447000·2017-07-14

    Mercedes-Benz Recalls 2017 Smart Fortwo Vehicles for Steering Knuckle Defect

    Mercedes-Benz USA is recalling 2017 Smart Fortwo and Cabriolet vehicles because casting imperfections in the left front axle steering knuckle could cause failure and increase crash risk.

    Product
    SMART — SMART FORTWO, FORTWO CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V444000·2017-07-14

    Keystone Recalls 2016-2018 Avalanche Trailers Due to Tire Hazard

    Keystone RV Company is recalling 2016-2018 Avalanche recreational trailers because a kitchen slide-out bolt could contact the front tire, potentially causing sudden tire failure and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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-2417-2017·2017-07-12

    Eatem Foods Recalls South African Style Spice Paste Due to Peanut Allergen

    Eatem Foods is recalling 10,650 pounds of South African Style Perl Perl Roasted Spice Paste because a supplier detected peanut allergen in an ingredient.

    Product
    SOUTH AFRICAN STYLE PERl PERl ROASTED SPICE PASTE INGREDIENTS: VINEGAR, JALAPENO PUR E;(jalapeno peppers, salt, vinegar), ONION, MINCED GARLIC (garlic, soybean oil, citric acid),PAPRIKA, CANOLA OIL, GRANULATED ONION, BIRDS EYE CHILl PEPPER, SALT,LEMON JUICE…
    Category
    Food
    Distribution
    0 states
  • 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 (Food)·F-2416-2017·2017-07-12

    Greek Pasta Salad Recalled for Undeclared Milk Allergen

    A.S.K. Foods is recalling Taste of Inspirations Greek Pasta Salad because some packages have incorrect labels that do not list milk as an ingredient.

    Product
    Taste of Inspirations; Greek Pasta Salad, Net Wt. 10 oz.; Distributed By: DZA Brands, LLC, Salisbury, NC 28147/Scarborough, ME 04074;
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-2424-2017·2017-07-12

    Smucker Foods Recalls Durum Atta Flour for Potential E. coli Contamination

    Smucker Foods of Canada Co. is recalling specific brands of Durum Atta Flour due to potential E. coli contamination reported by a co-packer.

    Product
    Flour sold under the following brands: Golden Temple Durum Atta Flour Blend, 20LB, DISTRIBUTED BY: SMUCKER FOODS OF CANADA CORP., MARKHAM, ON L3R 0P3 PRODUCT OF CANADA UPC 0 59000 41556 7, Swad Durum Atta Flour, 20 LB MILLED FOR: RAJA FOODS 8110 N. St. Louis Avenue Skokie, IL…
    Category
    Food
    Distribution
    13 states
  • 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 (Food)·F-2418-2017·2017-07-12

    Schnucks Bakery Cinnamon Pudding Cake Recalled for Undeclared Walnuts

    Schnucks Markets is recalling Cinnamon Pudding Cakes because the labels fail to declare the presence of walnuts, a major food allergen.

    Product
    1) Schnucks Bakery, Cinnamon Pudding Cake Slice, NET WT 6.0 oz (170 g); 2) Schnucks Bakery, Half Cinnamon Pudding Cake, NET WT 1.06 lb (482 g);
    Category
    Food
    Distribution
    5 states
  • 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