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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18776–18800 of 39605

  • CriticalFDA (Drugs)·D-0339-2018·2018-02-14

    Aurobindo Recalls Ampicillin and Sulbactam Injection Due to Glass Particulates

    Aurobindo Pharma is recalling 53,040 vials of Ampicillin and Sulbactam for Injection due to a confirmed report of visible glass particulate matter.

    Product
    AMPICILLIN AND SULBACTAM — AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0340-2018·2018-02-14

    AuroMedics Recalls Pantoprazole Sodium Injection Due to Glass Particulate

    AuroMedics Pharma LLC is recalling 66,100 vials of Pantoprazole Sodium for Injection because one vial contained a piece of glass.

    Product
    PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0768-2018·2018-02-14

    Vanilla Cake with Cheese Recalled for Undeclared Allergens

    Productos Pacheco, Inc. is recalling Vanilla Cake with Cheese due to undeclared allergens including wheat, soy, milk, and food dyes.

    Product
    Bizcocho de Vainilla con Queso [Vanilla Cake with Cheese] NET WT 4OZ and 12OZ
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0804-2018·2018-02-14

    Panera Chive and Onion Cream Cheese Spread Recalled for Listeria Risk

    Panera, LLC is recalling Chive & Onion Reduced Fat Cream Cheese Spread due to potential Listeria monocytogenes contamination.

    Product
    Panera Chive&Onion Reduced Fat Cream Cheese Spread, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0702-2018·2018-02-14

    Frog Holler Recalls Cherry Tomatoes for Potential Salmonella Contamination

    Frog Holler Ltd. is voluntarily recalling cherry tomatoes in pint clamshells due to potential Salmonella contamination. The product was distributed in Michigan between January 4 and 10, 2018.

    Product
    Cherry Tomatoes, packaged in a pint sized plastic clamshell, no labeling
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0757-2018·2018-02-14

    Mountain Rose Recalls Prickly Ash Bark Powder Due to Salmonella Risk

    Mountain Rose Inc is recalling Prickly Ash Bark Powder herbal supplements due to potential Salmonella contamination. The product was distributed in 30 states.

    Product
    Prickly Ash Bark Powder Herbal Supplement, packaged in food grade stand up plastic pouches or plastic bags depending on quantity ordered, various net weights - 1-oz., 4-oz., 8-oz., 1-lb., 2-lb., 5-lb., 7-lb., 11-lb., 15-lb., and 16-lb. The label is read in parts: "***Prickly…
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Devices)·Z-0508-2018·2018-02-14

    Siemens Artis Biplane Systems Recalled for Ceiling Mount Defect

    Siemens is recalling 265 Artis zee and Artis Q biplane systems because ceiling mount screws may not be fastened correctly.

    Product
    AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0559-2018·2018-02-14

    Recall of Emprint Percutaneous Antenna Due to Tip Disengagement Risk

    FDA is recalling Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 20cm (reinforced), Material CA20L2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0790-2018·2018-02-14

    Hiland Dairy Foods Recalls Tampico Citrus Punch Due to Undeclared Milk

    Hiland Dairy Foods is recalling 1,157 gallons of Tampico Citrus Punch because milk was detected in the product, despite not being listed on the label.

    Product
    Tampico Citrus Punch, 1 GAL (3.78 L) Tampico Beverages, Chicago, IL
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0762-2018·2018-02-14

    Mallorca Queso Recalled for Undeclared Soy Allergen

    Productos Pacheco, Inc. is recalling Mallorca Queso NET WT 4OZ because it contains undeclared soy. The product was distributed to consignees in Puerto Rico.

    Product
    Mallorca Queso NET WT 4OZ
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0558-2018·2018-02-14

    Recall of Covidien Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling the Covidien Emprint Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 20cm, Material CA20L1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0763-2018·2018-02-14

    Mallorca Guava Queso Recalled for Undeclared Soy and Potassium Sorbate

    Productos Pacheco, Inc. is recalling Mallorca Guava Queso because it contains undeclared soy and potassium sorbate. The product was distributed to consignees in Puerto Rico.

    Product
    Mallorca Guava Queso NET WT 4OZ
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0326-2018·2018-02-14

    Flawless Beauty Recalls Tatiomax Glutathione Whitening Kits Nationwide

    Flawless Beauty LLC is voluntarily recalling Tatiomax Glutathione Whitening kits nationwide because the products were marketed without FDA approval.

    Product
    Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2018·2018-02-14

    Panera Cream Cheese Recalled Due to Listeria Contamination Risk

    Panera, LLC is recalling Reduced-Fat Plain Cream Cheese (2 oz. and 8 oz.) because it may be contaminated with Listeria monocytogenes. The product was sold nationwide at Panera Cafes.

    Product
    Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·18098·2018-02-14

    ISO Beauty Recalls Ionic Pro Hair Dryers Due to Burn Hazard

    ISO Beauty is recalling Ionic Pro hair dryers because the cord can become brittle, posing a burn hazard. Consumers should stop using the units and contact the company for a refund.

    Product
    Ionic Pro hair dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0560-2018·2018-02-14

    Recall of Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling Emprint Percutaneous Antennas because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0759-2018·2018-02-14

    Mallorcas Pacheco Recalled for Undeclared Soy Allergen

    Productos Pacheco, Inc. is recalling Mallorcas Pacheco 1LB packages due to undeclared soy. The product was distributed to consignees in Puerto Rico.

    Product
    Mallorcas Pacheco NET WT 1LB (16OZ)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0322-2018·2018-02-14

    FDA Recalls Sterile Morphine Sulfate Preparations Due to Sterility Concerns

    Intrathecal Compounding Specialist, LLC is recalling sterile morphine sulfate preparations compounded between October 16 and November 17, 2017, due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Morphine Sulfate PF Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0328-2018·2018-02-14

    Flawless Beauty Recalls Unapproved Glutathione Injectable Products Nationwide

    Flawless Beauty LLC is voluntarily recalling all lots of Tationil Glutathione and other products sold in kits. The recall is due to misbranding and the sale of unapproved new drugs under a court order.

    Product
    Tationil Glutathione, 600 mg/ 4 mL, polvere e solvente per soluzione iniettabile, Teofarma, s.r.l.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0489-2018·2018-02-14

    Philips HeartStart MRx Defibrillators Recalled for Defective Component

    Philips is recalling 71 HeartStart MRx defibrillators because a defective component may prevent shock delivery in AED mode.

    Product
    MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0321-2018·2018-02-14

    FDA Recalls Hydromorphone Sterile Drug Preparations for Lack of Sterility Assurance

    Intrathecal Compounding Specialist is recalling sterile drug preparations made from Hydromorphone Base Solution due to a lack of sterility assurance.

    Product
    All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0770-2018·2018-02-14

    Vanilla Cake with Cheese and Guava Recalled for Undeclared Allergens

    Productos Pacheco, Inc. is recalling 12-ounce Vanilla Cake with Cheese and Guava due to undeclared allergens including wheat and soy.

    Product
    Bizcocho Vainilla con Queso y Guava [Vanilla Cake with Cheese and Guava] NET WT 12OZ
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0760-2018·2018-02-14

    Bread Recalled for Undeclared Soy Allergen in Puerto Rico

    Productos Pacheco, Inc. is recalling 1-pound loaves of bread sold in Puerto Rico because they contain undeclared soy.

    Product
    Pan [bread] NET WT 1LB (16OZ)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0332-2018·2018-02-14

    Flawless Beauty Recalls Sterilized Water for Injections Due to Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of sterilized water for injections sold in the U.S. because the products were marketed without FDA approval.

    Product
    Sterilized water for injections BP, 50 x 5 mL plastic ampules, Manufactured in India
    Category
    Drug
    Distribution
    Distributed nationwide