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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

25326–25350 of 114509

  • ModerateFDA (Drugs)·D-0418-2023·2023-03-08

    Vigabatrin Oral Solution Recalled for Manufacturing Quality Deviations

    Accord Healthcare is recalling 821 cartons of Vigabatrin for Oral Solution due to manufacturing quality deviations found during an FDA inspection. The product was distributed in the United States, Puerto Rico, and Canada.

    Product
    Vigabatrin for Oral Solution, USP, 500 mg, Rx Only, 50-packets/carton, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703 Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, INDIA. Packet NDC 16729-521-63, UPC 3 16729 52163 5; Carton NDC…
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0349-2023·2023-03-08

    Microcrystalline Cellulose Ingredient Recalled Over Failed Impurity Specifications

    DuPont Nutrition USA, Inc. is recalling certain batches of Avicel PH-101 microcrystalline cellulose because it failed quality testing for impurities and degradation. The ingredient showed out-of-specification conductivity levels.

    Product
    Avicel PH- 101 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp. Net Content/Gross Weight 50.0 KG / 54.5 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0386-2023·2023-03-08

    Prescription Doxazosin Tablets Recalled Due to Manufacturing Practice Deviations

    Accord Healthcare is recalling 44,068 bottles of Doxazosin 1 mg tablets distributed in the US, Puerto Rico, and Canada due to Current Good Manufacturing Practice deviations found during an FDA inspection.

    Product
    DOXAZOSIN — DOXAZOSIN (DOXAZOSIN)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0409-2023·2023-03-08

    Simvastatin tablets recalled due to manufacturing process deviations

    Accord Healthcare is recalling Simvastatin 10 mg tablets distributed in the U.S., Puerto Rico, and Canada due to manufacturing process deviations discovered during FDA inspection. Patients should contact their pharmacy or healthcare provider.

    Product
    SIMVASTATIN — SIMVASTATIN (SIMVASTATIN)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0419-2023·2023-03-08

    Pirfenidone tablets recalled due to manufacturing process deviations

    Accord Healthcare recalls Pirfenidone tablets due to manufacturing practice deviations found during FDA inspection. The recall affects 2,614 cartons distributed in the US, Puerto Rico, and Canada.

    Product
    PIRFENIDONE — PIRFENIDONE (PIRFENIDONE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0398-2023·2023-03-08

    Glycopyrrolate injection recalled due to manufacturing practice deviations

    Accord Healthcare recalls Glycopyrrolate injection due to manufacturing practice deviations found during FDA inspection. The recall affects 3,164 vials distributed in the US, Puerto Rico, and Canada.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0407-2023·2023-03-08

    Rosuvastatin tablets recalled for manufacturing quality control deviations

    Accord Healthcare is recalling rosuvastatin 40 mg tablets distributed in the US, Puerto Rico, and Canada due to manufacturing quality control deviations found during an FDA inspection. No illnesses have been reported.

    Product
    ROSUVASTATIN — ROSUVASTATIN (ROSUVASTATIN)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0371-2023·2023-03-08

    Prescription Drug Recall: Atorvastatin Calcium Tablets for Manufacturing Deviations

    Accord Healthcare is recalling Atorvastatin Calcium 10 mg tablets distributed in the United States, Puerto Rico, and Canada following FDA inspection findings of manufacturing deviations.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0395-2023·2023-03-08

    Accord Healthcare Recalls Glimepiride Tablets Due to CGMP Deviations

    Accord Healthcare is recalling Glimepiride 4 mg tablets due to Current Good Manufacturing Practice deviations discovered during an FDA inspection. Approximately 1.16 million bottles across the United States, Puerto Rico, and Canada are affected.

    Product
    GLIMEPIRIDE — GLIMEPIRIDE (GLIMEPIRIDE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0430-2023·2023-03-08

    Ropinirole Tablets Recalled Due to Manufacturing Practice Deviations

    Accord Healthcare is recalling 8,184 bottles of Ropinirole 4 mg tablets due to manufacturing practice deviations found during an FDA inspection. The recalled batches were distributed in the United States, Puerto Rico, and Canada.

    Product
    ROPINIROLE — ROPINIROLE (ROPINIROLE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-0388-2023·2023-03-08

    Hot chocolate and cappuccino products recalled for undeclared peanut allergen

    Corim Industries is recalling Agglomerated Peanut Butter Hot Chocolate and Peanut Butter Cappuccino products in multiple formats due to undeclared peanut allergen on the label.

    Product
    Smart Sips, 24 ct single serve coffee pods (12.7 oz carton)
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0420-2023·2023-03-08

    Pirfenidone Tablets Recalled Due to Manufacturing Compliance Deviations

    Accord Healthcare is recalling Pirfenidone 801 mg tablets due to Current Good Manufacturing Practice deviations identified during an FDA inspection. Affected batches P2202519 and P2202513 were distributed in the United States, Puerto Rico, and Canada.

    Product
    PIRFENIDONE — PIRFENIDONE (PIRFENIDONE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0352-2023·2023-03-08

    Microcrystalline Cellulose Pharmaceutical Excipient Recalled for Specification Failure

    DuPont Nutrition USA is recalling BD-102 NF Microcrystalline Cellulose, a pharmaceutical excipient, due to failed conductivity specifications. Affected batches were distributed nationwide and internationally for use in drug manufacturing.

    Product
    BD-102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp., Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0351-2023·2023-03-08

    Avicel PH-200 pharmaceutical excipient recalled for failed conductivity specification

    DuPont is recalling Avicel PH-200, a pharmaceutical excipient, because test results showed conductivity out of specification. No illnesses or injuries have been reported.

    Product
    Avicel PH-200 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V148000·2023-03-07

    Terex Advance Front Discharge Mixer Recall for Loose Axle Fasteners

    Terex Advance is recalling 2022 Front Discharge Mixer Commander vehicles because front-drive steer axle fasteners may not be tightened sufficiently, risking axle separation and loss of control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V149000·2023-03-07

    Kia K5 side curtain air bags may not deploy in crash

    Kia is recalling 2021-2023 K5 vehicles due to potentially incorrect installation of side curtain air bags that could prevent proper deployment in a crash.

    Product
    KIA — KIA K5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V147000·2023-03-06

    Newell Recalls 2023-2024 P50 Motor Coaches Due to Brake Light Defect

    Newell Coach Corp. is recalling 2023-2024 P50 motor coaches because brake lights may fail to illuminate unless the brake pedal is fully depressed, increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2023·2023-03-06

    Dahlia Imports Recalls Raw Bone-in Goat Products Lacking USDA Inspection

    Dahlia Imports is recalling approximately 196,019 pounds of raw bone-in goat products imported from Australia without the required USDA import reinspection.

    Product
    Dahlia Imports, LLC Recalls Raw Bone-in Goat Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·23V146000·2023-03-06

    2023 Triumph Bonneville T120 motorcycles recalled for brake disc detachment risk

    Triumph is recalling certain 2023 Bonneville T120 motorcycles because the left-hand side brake disc may detach, reducing brake performance and increasing crash risk. Dealers will install replacement parts free of charge.

    Product
    TRIUMPH — TRIUMPH BONNEVILLE T120
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·006-2023·2023-03-04

    GH Foods Recalls Trader Joe's Lemon Chicken Salad Due to Undeclared Wheat

    GH Foods NW, LLC is recalling approximately 106 pounds of Trader Joe's Lemon Chicken & Arugula Salad because the label fails to declare wheat, a known allergen.

    Product
    F&S Produce West LLC — GH Foods NW, LLC Recalls Ready-to-Eat Salad with Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V145000·2023-03-03

    Xos Recalls 275 Vehicles Due to Driveshaft Bolt Tightening Defect

    Xos is recalling 275 RM01, SA01, and SV05 vehicles because improperly tightened bolts may allow the driveshaft to separate, increasing crash risk.

    Product
    XOS — XOS SV05, SA01, RM01
    Category
    Vehicle
    Distribution
    Distributed nationwide