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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17326–17350 of 39601

  • SevereFDA (Food)·F-1905-2018·2018-09-05

    Ararat Cut Beets Recalled Due to High pH Levels

    Artashes LLC is recalling Ararat Cut Beets because FDA inspections found pH levels above the scheduled process.

    Product
    Ararat Cut Beets; 19 oz. glass jar; Ingredients: Cut Beets, Water, Salt, Sugar, Citric Acid. Product of Armenia; Exclusively imported and distributed by: Kradjian Importing Co., Inc. Glendale, CA
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1141-2018·2018-09-05

    Torrent Pharma Recalls Amlodipine, Valsartan, and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling specific batches of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Amlodipine, Valsartan and Hydrochlorothiazide Tablets, USP, 10 mg/320 mg/25 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-325-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·074-2018·2018-09-04

    Bahar LLC Recalls Frozen Raw Beef Dumplings Produced Without Inspection

    Bahar LLC is recalling approximately 2,520 pounds of frozen, raw beef dumplings produced without federal inspection. The products were distributed in New Jersey.

    Product
    Bahar, LLC — Bahar LLC Recalls Frozen, Raw Beef Dumpling Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·073-2018·2018-08-31

    J.T.M. Provisions Recalls Cooked Ground Beef Patties Due To Listeria

    J.T.M. Provisions is recalling approximately 960 pounds of cooked ground beef patty products due to possible Listeria monocytogenes contamination. The products were shipped to distribution centers in California.

    Product
    J T M Provisions Company — J.T.M. Provisions Company Recalls Cooked Ground Beef Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·072-2018·2018-08-30

    Publix Recalls Ground Chuck Products Due To Possible E. coli O26 Contamination

    Publix Super Markets is voluntarily recalling ground chuck products sold in Florida from June 25 to July 31, 2018, due to possible E. coli O26 contamination linked to 18 illnesses.

    Product
    Publix Supermarkets, Inc., Deli Plant — Publix Super Markets Inc. Recalls Ground Chuck Products Due To Possible E. coli O26 Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V578000·2018-08-30

    GM Recalls 2015-2016 Trucks and SUVs for Brake Pedal Nut Issue

    General Motors is recalling 2015-2016 Chevrolet and GMC vehicles because a brake pedal pivot nut may loosen, potentially rendering the brakes inoperative or interfering with the accelerator.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 3500, SIERRA 2500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V581000·2018-08-30

    Daimler Trucks Recalls 2017-2019 Freightliner and Western Star Trucks for Fuel Line Defect

    Daimler Trucks is recalling 2017-2019 Freightliner and Western Star trucks because a restricted fuel pump cooling circuit screen may cause the fuel line to burst, leading to fuel leaks or engine stalling.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 122SD, CASCADIA, CORONADO, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V576000·2018-08-30

    GM Recalls 2018-2019 Vehicles for Rear Brake Caliper Coating Defect

    General Motors is recalling 2018-2019 Chevrolet, GMC, Buick, and Cadillac vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, BUICK IMPALA, VOLT, XTS, BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V570000·2018-08-30

    Jayco Recalls 2018 Alante Vehicles Due to Hydraulic Hose Fire Risk

    Jayco is recalling 2018 Alante vehicles because damaged leveling system hydraulic hoses may leak fluid onto the exhaust system, increasing the risk of a fire.

    Product
    JAYCO — JAYCO ALANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18212·2018-08-30

    PetSmart Recalls Reptile Strip Lights Due to Fire Hazard

    PetSmart is recalling 20-inch and 30-inch reptile strip light fixtures because the bulbs can overheat and ignite the hood, posing a fire hazard.

    Product
    Reptile strip light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1840-2018·2018-08-29

    Peanut Paste and Butter Recalled Due to Salmonella Test Results

    Peanut Processors, Inc. is recalling bulk peanut paste and butter after a customer reported the product tested positive for Salmonella.

    Product
    Peanut Paste/Butter bulk tankers
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1178-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Thyroid Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling specific lots of Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-156-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1180-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-155-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1181-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/4 grain (15 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-159-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1839-2018·2018-08-29

    Sherman Candy Caramels Recalled for Undeclared Tree Nuts and Peanuts

    Gift Services Inc is recalling Sherman Candy Caramels found in specific gourmet gift baskets due to undeclared pecans, walnuts, almonds, and/or peanuts.

    Product
    Sherman Candy Caramels are individually wrapped in plastic and then sealed in a cardboard flexible carton. Each Sherman Candy Caramels contains 3 pieces inside and sold in the following gift baskets: Metropolitan Gourmet Gift Basket. Encore Gourmet Gift Basket. Toast of…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1846-2018·2018-08-29

    Salt & Straw Recalls Chocolate Gooey Brownie Ice Cream for Undeclared Peanuts

    Salt & Straw LLC is recalling specific lots of Chocolate Gooey Brownie Ice Cream due to possible undeclared peanuts. Consumers should check lot numbers and stop eating the product.

    Product
    Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3 gal. tubs. 3 gal. tubs were sold to Salt & Straw Retail Scoop Shops only. 1 gal. containers are sold to wholesale accounts only.
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Drugs)·D-1179-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 & 1/2 grain (90 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-157-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1182-2018·2018-08-29

    FDA Recalls Levothyroxine and Liothyronine Thyroid Tablets Due to Content Uniformity Failures

    Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications, potentially resulting in incorrect drug strength.

    Product
    Levothyroxine and Liothyronine (Thyroid Tablets, USP), 2 grain (120 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-158-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·070-2018·2018-08-29

    Taylor Farms Recalls Beef and Pork Meatloaf for Undeclared Allergens

    Taylor Farms Illinois is recalling beef and pork meatloaf products due to misbranding and undeclared eggs and wheat. No adverse reactions have been reported.

    Product
    Taylor Farms Illinois, Inc — Taylor Farms Illinois, Inc. Recalls Beef and Pork Meatloaf Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1832-2018·2018-08-29

    HP Hood Recalls Blue Diamond Almond Milk Due to Milk Allergen

    HP Hood LLC is recalling Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.

    Product
    Blue Diamond Almond Breeze Almond Milk, Half Gallon
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2843-2018·2018-08-29

    Philips DigitalDiagnost 4.1 Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost 4.1 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to operators and patients.

    Product
    DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·18211·2018-08-29

    Cybex Smith Press Weight-Lifting Equipment Recalled Due to Serious Injury Hazards

    Cybex is recalling Smith Press models 5340 and 5341 because the weight bar can fall, posing serious injury hazards. Consumers should stop using the equipment and contact Cybex for a repair or refund.

    Product
    Cybex Smith Press plate-loaded weight-lifting equipment
    Category
    Consumer Product
    Distribution
    Distributed nationwide