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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3051–3075 of 7451

  • CriticalFDA (Drugs)·D-0970-2017·2017-07-19

    FDA Recalls ZRECT for Women Herbal Supplement Due to Undeclared Drugs

    Organic Herbal Supply is recalling ZRECT for Women herbal capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229055
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0961-2017·2017-07-19

    UPROAR Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling UPROAR male enhancement capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules, supplied in 2, 4 and 10 count packages, Distributed by AH Distribution, DelRay, Beach, FL ---- UPC Code 680474229260
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2541-2017·2017-07-19

    Wildway Coconut Cashew Granola Recalled for Listeria Risk

    Wildway LLC is recalling specific lots of Coconut Cashew Grain-free Granola due to potential contamination with Listeria monocytogenes.

    Product
    Wildway Coconut Cashew Grain-free Granola 8 oz. and 10 oz. UPC: 858660005183 packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2398-2017·2017-07-19

    Pacific Wave Yellow Fin Tuna Loins Recalled for Hepatitis A

    P & E Foods Inc is recalling Pacific Wave Yellow Fin Tuna loins after testing revealed a positive result for Hepatitis A.

    Product
    Pacific Wave Yellow Fin Tuna loins; 30 lb. cases. Product of Indonesia; Imported by Unified Seafood Co., Inc.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0965-2017·2017-07-19

    Rectalis Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling Rectalis Male Enhancement Capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    RECTALIS Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY --- UPC Code 680474228782
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0964-2017·2017-07-19

    Xrect Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling Xrect Male Enhancement capsules because FDA analysis found undeclared prescription drugs tadalafil, sildenafil, and Flibanserin.

    Product
    Xrect Male Enhancement Herbal Dietary Supplement Capsules, 500 mg supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA ---- UPC Code 680474015795
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0969-2017·2017-07-19

    Enhancerol Herbal Supplement Recalled for Undeclared Prescription Drug Ingredients

    Organic Herbal Supply is recalling Enhancerol Herbal Dietary Supplement Capsules because FDA analysis found undeclared tadalafil, sildenafil, and Flibanserin.

    Product
    ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0966-2017·2017-07-19

    Tornado Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling Tornado Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    TORNADO Male Enhancement Herbal Dietary Supplement Capsules, Over 4000 mg value, supplied in 2, 4 and 10 count packages, Made in USA Distributed by American Health Supplements, Chicago, Illinois --- UPC Code 680474228959
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0967-2017·2017-07-19

    FDA Recalls ZDaily Testosterone Supplement for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling ZDaily Testosterone and Libido Booster capsules because FDA analysis found undeclared prescription drugs, including tadalafil, sildenafil, and flibanserin.

    Product
    ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229062
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2577-2017·2017-07-19

    Kroger Simple Truth Macadamia Nuts Recalled for Listeria

    Kroger is recalling Simple Truth Dry Roasted Macadamia Nuts due to an expanded supplier notification regarding Listeria monocytogenes.

    Product
    Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202
    Category
    Food
    Distribution
    32 states
  • CriticalFDA (Drugs)·D-0971-2017·2017-07-19

    LabidaMAX Herbal Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling LabidaMAX Herbal Dietary Supplement Capsules because FDA analysis found undeclared prescription drugs.

    Product
    LabidaMAX Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY --- UPC Code 680474228904
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2534-2017·2017-07-19

    Smokehouse of NY Recalls Smoked Norwegian Fish for Listeria Risk

    The Smokehouse of New York is recalling smoked Norwegian fish due to potential Listeria monocytogenes contamination. The product was distributed in six states.

    Product
    The Smokehouse of NY Smoked Norwegian Fish packaged as: 4oz & 8oz and whole sides
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0968-2017·2017-07-19

    FDA Recalls BIGnHARD Male Enhancement Capsules for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling BIGnHARD Male Enhancement Capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    BIGnHARD Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0962-2017·2017-07-19

    FDA Recalls Cummor Male Enhancement Supplement for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling Cummor Natural Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    Cummor Natural Male Enhancement, Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Naturally Hard Supplements, Reno, NV --- UPC code #680474229116
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0963-2017·2017-07-19

    ZRECT Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling ZRECT Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    ZRECT Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 852675999451
    Category
    Drug
    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
  • CriticalNHTSA·17E034000·2017-07-10

    Takata Driver Frontal Air Bag Inflator Recall for Rupture Risk

    Takata is recalling specific driver-side air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2391-2017·2017-07-05

    IFF Seasoning Blends Recalled Due to Potential Salmonella Contamination

    International Flavors & Fragrances, Inc. is recalling seasoning blends that may contain salmonella. The affected products were distributed in Texas and Canada.

    Product
    Seasoning blends IFF Inc. Carrollton 1620 West Crosby Carrollton TX 75006 Net Weight 50.00 LBS 22.680
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-2393-2017·2017-07-05

    Ava's Organic Cashews Recalled Due to Listeria Contamination Risk

    Severn Peanut Co. is recalling Ava's brand Organic Cashews Roasted & Salted 8 oz. tubs because the product may be contaminated with Listeria monocytogenes.

    Product
    Ava's brand Organic Cashews Roasted & Salted 8 oz. tubs, UPC 8-10111-01035-1
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-2410-2017·2017-07-05

    Global Garlic Queso Fresco Recalled for Listeria Contamination

    Global Garlic, Inc. is recalling Queso Fresco cheese contaminated with Listeria monocytogenes. The product was distributed to Florida, Illinois, Kentucky, Louisiana, and North Carolina.

    Product
    Queso Fresco x LB (Barra)/ Whole Milk Cheese, Net Wt 5-6 lbs.
    Category
    Food
    Distribution
    5 states
  • CriticalCPSC·17182·2017-06-28

    South Shore Recalls 5-Drawer Chests Due to Tip-Over Hazard

    South Shore Industries is recalling about 68,300 Summer Breeze style 5-drawer chests because they are unstable and can tip over if not anchored to the wall. Consumers should stop using the chests until they are secured or contact the company for a refund or free restraint kit.

    Product
    5-drawer chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·076-2017·2017-06-23

    Wornick Company Recalls Beef Ravioli Due to Undeclared Milk Allergen

    The Wornick Company is recalling beef ravioli products because they may contain undeclared milk, a known allergen, which is not listed on the label.

    Product
    The Wornick Company — The Wornick Company Recalls Beef Ravioli Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide