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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11926–11950 of 17785

  • LowFDA (Drugs)·D-1036-2016·2016-06-22

    Sandoz Recalls Lisinopril Tablets Due to Missing Package Insert

    Sandoz Inc is recalling 3,048 bottles of Lisinopril Tablets USP, 30 mg, because the package insert is incorrect or missing.

    Product
    Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0966-2016·2016-06-15

    FDA Recalls Thin and Slim Thermogenic Fat Burner for Unapproved Ingredient

    Novacare, LLC is recalling The Store Thin and Slim Thermogenic Fat Burner because FDA sampling found salicylic acid, an ingredient not approved for dietary supplements.

    Product
    The Store Thin and Slim Thermogenic Fat Burner Dietary Supplement packaged in 90 capsule containers. Distributed by The Store 2050 E. 6200 S., Holladay, UT 84121, The Store Holliday, 4695 S.Holladay Blvd, Holladay, UT 84117, The Store Midway, 42 W. Main Street, Midway, UT 84049.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0964-2016·2016-06-15

    Novacare Recalls MetaPro 360 Supplement Containing Unapproved Salicylic Acid

    Novacare, LLC is recalling MetaPro 360 Metabolic Accelerator dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug ingredient.

    Product
    MetaPro 360 Metabolic Accelerator Dietary Supplement packaged in 120 capsule containers. www.metapro360.com 877-778-7509.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0970-2016·2016-06-15

    FDA Recalls Asia Black 25 Ephedra Extreme Fat Burner for Unapproved Ingredients

    Novacare, LLC is recalling Asia Black 25 Ephedra Extreme Fat Burner because FDA sampling confirmed the presence of salicylic acid, an unapproved ingredient in dietary supplements.

    Product
    Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0960-2016·2016-06-15

    Fuel Up High Octane capsules recalled for undeclared sildenafil analogue

    Reesna, Inc. is recalling Fuel Up High Octane capsules because they contain undeclared hydroxythiohomosildenafil, an analogue of the prescription drug Sildenafil.

    Product
    FUEL UP HIGH OCTANE, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0957-2016·2016-06-15

    Baxter Recalls Sodium Chloride Injection Due to Insect Particulate Matter

    Baxter Healthcare is recalling 255,852 bags of 0.9% Sodium Chloride Injection because customers reported finding an insect in the primary container.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0962-2016·2016-06-15

    FDA Recalls Thermo FX Supplement for Unapproved Salicylic Acid

    Novacare, LLC is recalling The People's Chemist Thermo FX Barely Legal Thermogenic Aid because FDA sampling confirmed the presence of salicylic acid in the product.

    Product
    The People's Chemist Thermo FX Barely Legal Thermogenic Aid, packaged in 90 capsule containers. Manufactured by TPC, LLC, www.thepeopleschemist.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0959-2016·2016-06-15

    Fuel Up Plus capsules recalled for undeclared sildenafil analogue

    Reesna, Inc. is recalling Fuel Up Plus capsules marketed as a dietary supplement because they contain undeclared hydroxythiohomosildenafil, an analogue of the ED drug sildenafil.

    Product
    FUEL UP PLUS, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1010-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls SUPER TRI-MIX #4 Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling 869 vials of SUPER TRI-MIX #4 because FDA inspections found violations that may affect sterility.

    Product
    SUPER TRI-MIX #4, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1025-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls QUAD-MIX #3 Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling QUAD-MIX #3 vials because FDA inspections found violations that may affect product sterility.

    Product
    QUAD-MIX #3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0965-2016·2016-06-15

    FDA Recalls Thin and Slim Burn Fat Now Supplement for Unapproved Ingredient

    Novacare, LLC is recalling Thin and Slim Burn Fat Now dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug ingredient.

    Product
    Thin and Slim Burn Fat Now Dietary Supplement packaged in 90 capsule containers. http://www.secretsofherbs.com. Made in the USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0988-2016·2016-06-15

    FDA Recalls 1-HCG 1000 IU/ML Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling 1-HCG 1000 IU/ML vials because FDA inspections identified GMP violations that may impact product sterility.

    Product
    1-HCG 1000 IU/ML, packaged in 5mL and 10mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0958-2016·2016-06-15

    Baxter Recalls Dextrose Injection Due to Insect Contamination

    Baxter Healthcare is recalling Dextrose Injection, USP, 70% due to confirmed reports of an insect found in the primary container.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0963-2016·2016-06-15

    FDA Recalls MaxOut Body Fat Burner for Unapproved Salicylic Acid

    Novacare, LLC is recalling MaxOut Body Fat Burner with Ephedra because FDA sampling confirmed the presence of salicylic acid in the dietary supplement.

    Product
    Thin and Slim MaxOut Body Max Out FX Fat Burner with Ephedra packaged in containers of 60 capsules. Distributed by Teamtrade, Inc., Ft. Lauderdale, FL. 1-866-MaxOut www.MaxOutBODY.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1006-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls QUAD-MIX #1 Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling QUAD-MIX #1 vials because FDA inspections found violations that may affect sterility.

    Product
    QUAD-MIX #1, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0984-2016·2016-06-15

    Estradiol Valerate Recall Due to Sterility Assurance Concerns

    Well Care Compounding Pharmacy is recalling Estradiol Valerate 40mg/mL vials because FDA inspections found GMP violations that may affect sterility.

    Product
    ESTRADIOL VALERATE 40MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0983-2016·2016-06-15

    Estradiol Valerate Recall Due to Sterility Assurance Concerns

    Well Care Compounding Pharmacy is recalling Estradiol Valerate 20mg/mL vials due to GMP violations affecting sterility.

    Product
    ESTRADIOL VALERATE 20MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1027-2016·2016-06-15

    FDA Recalls Itraconazole and Mupirocin Nasal Spray Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling Itraconazole 0.2%/Mupirocin 0.2% Nasal Spray because FDA inspections found GMP violations that may affect sterility.

    Product
    ITRACONAZOLE 0.2%/MUPIROCIN 0.2% NASAL SPRAY; 30 mL Spray, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0985-2016·2016-06-15

    Gentamicin Ophthalmic Solution Recalled for Sterility Assurance Concerns

    Well Care Compounding Pharmacy is recalling Gentamicin 15 mg/ml Ophthalmic Solution due to FDA inspection findings regarding sterility assurance.

    Product
    GENTAMICIN 15 MG/ML Ophthalmic Solution, Sterile Droppers, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1026-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls Otic Solution Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling specific lots of Clotrimazole 1%/Betamethasone Dipropionate 0.05% Otic Solution because FDA inspections found GMP violations that may affect sterility.

    Product
    CLOTRIMAZOLE 1%/ BETAMETHASONE DIPROPIONATE 0.05% OTIC SOLUTION, 15mL dropper, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1000-2016·2016-06-15

    Methylcobalamin Injection Recalled Due to Sterility Assurance Concerns

    Well Care Compounding Pharmacy is recalling Methylcobalamin 1 mg/mL vials because FDA inspections found GMP violations that may impact product sterility.

    Product
    METHYLCOBALAMIN 1 MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0968-2016·2016-06-15

    Dietary Supplement Recalled for Unapproved Salicylic Acid Content

    Novacare, LLC is recalling Thin and Slim Naturally AM dietary supplements because FDA sampling confirmed the presence of unapproved salicylic acid.

    Product
    Thin and Slim Naturally The Natural Alternative AM Dietary Supplement packaged in 90 capsule containers. Distributed by TSN Labs Inc., P.O. Box 38, Midvale, UT 84047, 1-800-769-7290, www.tsn2000.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0997-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls Injectable Vitamin Mixture for Sterility Concerns

    Well Care Compounding Pharmacy is recalling 869 vials of a compounded injectable vitamin mixture due to FDA inspection findings that raised concerns about product sterility.

    Product
    MB 12/HXB 12/FA/P5P/(LIDO 0.1 %), 2MG/2MCi/20MG/6.5MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1018-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls TRI-MIX # 3 Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling TRI-MIX # 3 vials because FDA inspections found GMP violations that may affect sterility.

    Product
    TRI-MIX # 3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state