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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17426–17450 of 39601

  • SevereFDA (Drugs)·D-1097-2018·2018-08-22

    Northwind Pharmaceuticals Recalls Valsartan 80mg Due to Carcinogen Impurity

    Northwind Pharmaceuticals is recalling Valsartan 80mg tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Valsartan, 80mg, 30 tablets per bottle, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC: 51655-0652-52
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1102-2018·2018-08-22

    RemedyRepack Recalls Valsartan 320 mg Tablets Due to Carcinogen Impurity

    RemedyRepack Inc. is recalling specific lots of Valsartan 320 mg tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Valsartan 320 mg Tablets, HDPE 90 cc bottles in cardboard trays, Rx Only, RemedyRepack, Inc., 625 Kolter Drive, Suite 4, Indiana, PA 15701, NDC 61786-0793-19
    Category
    Drug
    Distribution
    2 states
  • CriticalUSDA FSIS·068-2018·2018-08-21

    Taylor Farms Recalls Meatloaf Due To Undeclared Allergens

    Taylor Farms Northwest is recalling 62 pounds of ready-to-eat meatloaf containing undeclared fish and milk allergens. The products were distributed in Oregon and Washington.

    Product
    Taylor Farms Northwest LLC — Taylor Farms Northwest, LLC Recalls Ready-To-Eat Meatloaf Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereCPSC·18198·2018-08-21

    Confer Plastics Recalls Pool Step Systems Due to Entrapment Hazard

    Confer Plastics is recalling Curve in-pool step systems because children's limbs can become entrapped in side openings, posing a drowning risk.

    Product
    Curve in-pool step systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V551000·2018-08-21

    Nissan and Chevrolet Recall for Ignition Switch Stalling Risk

    Nissan is recalling 2017-2018 models including the Versa, Sentra, and NV200 because the ignition switch may shift, causing the engine to stall and increasing crash risk.

    Product
    NISSAN — NISSAN, CHEVROLET VERSA NOTE, NV200 TAXI, VERSA, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V548000·2018-08-20

    Ford Recalls 2018-2019 Vehicles for Electrical Arc Fire Risk

    Ford is recalling 2018-2019 Edge, Flex, MKX, and MKT vehicles because improperly secured power supply cables may cause an electrical arc, increasing the risk of a fire.

    Product
    FORD — FORD, LINCOLN EDGE, MKX, MKT, FLEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V545000·2018-08-17

    2019 Coachmen Freedom Express Recalled for Brake Wiring Defect

    Forest River is recalling 2019 Coachmen Freedom Express trailers because the break-away safety switch may not engage brakes if the trailer detaches.

    Product
    COACHMEN — COACHMEN FREEDOM EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V546000·2018-08-17

    Winnebago Recalls 2016-2019 Motorhomes Due to Unfused Solar Charging Circuit

    Winnebago is recalling 2016-2019 motorhomes because an unfused auxiliary solar charging circuit can increase the risk of fire if solar panels exceed the circuit's amperage capacity.

    Product
    WINNEBAGO — WINNEBAGO TREND, PASEO, JOURNEY, ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V539000·2018-08-16

    Mercedes-Benz Recalls 2018 GLE and GLS Models for Brake Defect

    Mercedes-Benz is recalling 9,044 2018 GLE and GLS vehicles because rear brake caliper pistons may release gas, reducing braking performance.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE43, GLS 450, AMG GLE63S, GLS 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V542000·2018-08-16

    Volvo Recalls 2019 VNL and VNR Trucks for Fifth Wheel Defect

    Volvo is recalling 2019 VNL and VNR trucks because a narrow fifth wheel bracket may allow the trailer to separate from the tractor, increasing crash risk.

    Product
    VOLVO — VOLVO VNL, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V543000·2018-08-16

    Mack Recalls 2019 Anthem Trucks Due to Fifth Wheel Bracket Defect

    Mack Trucks is recalling 2019 Anthem trucks with Jost fifth wheel couplings because a narrow slider bracket may allow the trailer to separate, increasing crash risk.

    Product
    MACK — MACK ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1930-2018·2018-08-15

    Hy-Vee Spring Pasta Salad Recalled for Salmonella Illness Risk

    D & D Foods, Inc. is recalling Hy-Vee Spring Pasta Salad due to an outbreak of Salmonella Sandiego and Salmonella enterica subspecies IIIb illness potentially associated with the product.

    Product
    Hy-Vee Spring Pasta Salad packaged in the following containers: 1) plastic tubs with lids, Net Wt 16 OZ (454 g); 2) plastic tubs with lids, Net Wt 48 OZ (3 LB) 1.36 kg; 3) 4/8 lb cases Net Wt 32.00 LBS (14.51 KG); 4) 8 lb cases Net WT. 8.00 LBS (3.63 KG); 5) 11 lb Spring Salad…
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1742-2018·2018-08-15

    Whole Foods Bakery Products Recalled for Undeclared Soy Flour

    Whole Foods Market is recalling bakery products sold in the Mid-Atlantic region between May 25 and July 13 because they failed to declare soy flour as an ingredient.

    Product
    CAKE TOASTED ALMOND 6 IN, 29.6 Ounce CAKE TOASTED ALMOND 9IN, 64.0 Ounce
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-1125-2018·2018-08-15

    World Organix Recalls Blissful Remedies Capsules for Microbial Contamination

    World Organix LLC is recalling Blissful Remedies Gold Series Ultra Enhanced Indo capsules due to potential high microbial loads.

    Product
    Blissful Remedies Gold Series Ultra Enhanced Indo, 50 capsule, packaged in While Foil Pouch, Dist. by World Organix LLC, Las Vegas Nevada UPC# 6 02401 88900 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1760-2018·2018-08-15

    Lipari Foods Recalls Turkey and Swiss Submarine Sandwiches for Listeria Risk

    Lipari Foods is voluntarily recalling Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1834-2018·2018-08-15

    Sweet Earth Aloha BBQ Quesadilla Recalled for Undeclared Allergens

    Sweet Earth Inc. is recalling Aloha BBQ Quesadillas because some packages contain Mile High Quesadillas with undeclared eggs and milk.

    Product
    Sweet Earth Foods Aloha BBQ Quesadilla; 2 pack, NET WT 8 oz. Vegan: Pinto Beans, Red Onions, Pineapple and jalapenos with our vegan BBQ grounds and a cheddar-style vegan cheese. Keep Frozen. Ingredients: Filling: Vegan BBQ savory grounds (water, vital wheat gluten…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1744-2018·2018-08-15

    Whole Foods Bakery Products Recalled for Undeclared Soy Flour

    Whole Foods Market is recalling Italian Rum cakes from Mid-Atlantic stores sold between May 25 and July 13, 2018, due to undeclared soy flour.

    Product
    CAKE ITALIAN RUM 6IN CAKE ITALIAN RUM 9IN
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1063-2018·2018-08-15

    Guardian Pharmacy Recalls Fentanyl Citrate Syringes Due to Sterility Concerns

    Guardian Pharmacy Services is recalling 300 syringes of Fentanyl Citrate 50 mcg/mL in Texas due to a lack of sterility assurance.

    Product
    Fentanyl Citrate 50 mcg/mL 2ml. Rx Only. Packaged in 2 mL syringes. Compounded Guardian Pharmacy Services, 7920 Elmbrook Dr. Ste. 108C Dallas TX 75247
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1747-2018·2018-08-15

    Whole Foods Recalls Bakery Products for Undeclared Soy Flour

    Whole Foods Market is recalling bakery products sold in the Mid-Atlantic region between May 25 and July 13 because they failed to declare soy flour as an ingredient.

    Product
    CAKE MANGO MOUSSE 9IN
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2553-2018·2018-08-15

    Vyaire Medical Recalls Pediatric AirLife Resuscitation Devices Due to Airflow Obstruction Risk

    Vyaire Medical is recalling 15,714 pediatric AirLife Resuscitation Devices because a manufacturing error may obstruct supplemental oxygen airflow during use.

    Product
    AirLife Resuscitation Device, Pediatric labeled as the following: a. Pediatric, with mask, 28" large bore tubing, pressure-relief valve, Part Number 2K8018; b. Pediatric, with mask, 40" oxygen reservoir bag, pressure-relief valve, Part Number 2K8008; c. Pediatric…
    Category
    Medical Device
    Distribution
    28 states
  • SevereFDA (Drugs)·D-1058-2018·2018-08-15

    Guardian Pharmacy Recalls Hyaluronidase Vials Due to Sterility Concerns

    Guardian Pharmacy Services is recalling Hyaluronidase 150 units/mL vials in Texas due to a lack of sterility assurance.

    Product
    Hyaluronidase 150 units/mL 1ml. Rx Only. Packaged in 1 mL vials. Compounded Guardian Pharmacy Services, 7920 Elmbrook Dr. Ste. 108C Dallas TX 75247
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1123-2018·2018-08-15

    World Organix Recalls Blissful Remedies Herbal Shot Due to Microbial Contamination

    World Organix, LLC is recalling Blissful Remedies 4 Hour Chill herbal shots due to potential high microbial loads. The affected products were distributed nationwide.

    Product
    Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot. 1.93 Fluid Oz (57ml) UPC#6 02401 88900 3.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1736-2018·2018-08-15

    Whole Foods Recalls Bakery Products for Undeclared Soy Flour

    Whole Foods Market is recalling specific bakery products sold in the Mid-Atlantic region between May 25 and July 13 because they failed to declare soy flour as an ingredient.

    Product
    CUPCAKE BERRY CHANTILLY MEDIUM, 4.5 Ounce
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1071-2018·2018-08-15

    Guardian Pharmacy Recalls Methylcobalamin Vials Due to Sterility Concerns

    Guardian Pharmacy Services is recalling 2,000 vials of compounded Methylcobalamin 1000 mcg/mL in Texas due to a lack of sterility assurance.

    Product
    Methylcobalamin 1000 mcg/mL 100 mL. RX Only. Packaged in 100ml MDV vials. Compounded Guardian Pharmacy Services, 7920 Elmbrook Dr. Ste. 108C Dallas TX 75247
    Category
    Drug
    Distribution
    1 state