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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12151–12175 of 17987

  • HighFDA (Drugs)·D-0981-2016·2016-06-15

    FDA Recalls Estradiol Cypionate Vials Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling Estradiol Cypionate 10 mg/mL vials because FDA inspections found GMP violations that may affect sterility.

    Product
    ESTRADIOL CYPIONATE 10 MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0956-2016·2016-06-15

    Novo Nordisk Recalls Norditropin Pens Due to Delivery System Defect

    Novo Nordisk is recalling 723 Norditropin FlexPro pens due to a potential assembly fault that may cause the pen to block during the air shot step.

    Product
    NORDITROPIN — NORDITROPIN (SOMATROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1017-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls TRI-MIX # 2 Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling TRI-MIX # 2 vials because FDA inspections found violations that may affect sterility.

    Product
    TRI-MIX # 2, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0994-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls M.l.C. Vials Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling M.l.C. 25mg/50mg/25mg/mL vials because FDA inspections found GMP violations that may affect sterility.

    Product
    M.l.C. 25MG/50MG/25MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0975-2016·2016-06-15

    Aidarex Recalls Chlorhexidine Gluconate Oral Rinse Due to Impurity

    Aidarex Pharmaceuticals is recalling 292 bottles of Chlorhexidine Gluconate 0.12% Oral Rinse because the product failed impurity specifications.

    Product
    CHLORHEXIDINE GLUCO. 0.12% ORAL RINSE, Packaged in 473 ML Bottles, Rx Only. MFG: HI-TECH PHARMACAL CO., INC., AMITYVILLE, NY 11701, Packaged By: Aidarex PHARMACEUTICALS. NDC: 33261-0447-01.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0991-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls Hydrogen Peroxide Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling 869 units of Hydrogen Peroxide 3% due to FDA inspection findings regarding sterility assurance.

    Product
    Hydrogen Peroxide 3%, packaged in 10mL bottles, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0989-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls 1-HCG 2000 IU/ML Vials

    Well Care Compounding Pharmacy is recalling 1-HCG 2000 IU/ML vials due to GMP violations that may affect sterility.

    Product
    1-HCG 2000 IU/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0980-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls Atropine Sulfate Ophthalmic Drops

    Well Care Compounding Pharmacy is recalling Atropine Sulfate 0.5% Ophthalmic Drops due to FDA inspection findings of GMP violations that may impact sterility.

    Product
    ATROPINE SULFATE 0.5% Ophthalmic Drops, packaged in 5mL droppers, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0976-2016·2016-06-15

    Pharmedium Recalls Potassium Chloride Injection Bags Due to Labeling Error

    Pharmedium Services is recalling 240 bags of Potassium Chloride Injection due to a labeling error where Potassium Phosphate was printed on the label stock.

    Product
    Potassium CHLORide added to 5% Dextrose Injection, 20 mEq 250 mL Bag, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141, NDC 61553-836-11, Service Code 2K5836.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1021-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls TRI-MIX # 6 Due to Sterility Concerns

    Well Care Compounding Pharmacy is recalling TRI-MIX # 6 vials because FDA inspections found violations that may affect product sterility.

    Product
    TRI-MIX # 6, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0977-2016·2016-06-15

    Bayer Recalls Coppertone Sunscreen Lotion for Undeclared Oxybenzone

    Bayer Health Care LLC is recalling 37,512 bottles of Coppertone Sunscreen Lotion, Clearly Sheer, Broad Spectrum SPF 50, because the product contains undeclared Oxybenzone.

    Product
    Coppertone SUNSCREEN LOTION, CLEARLY SHEER, BROAD SPECTRUM SPF 50, 5 FL OZ (147mL), OTC, Dist by: Bayer HealthCare LLC, Whippany, NJ 07981 --- NDC 11523-7391-1, UPC 00041100005762
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0999-2016·2016-06-15

    Well Care Compounding Pharmacy Recalls Methylcobalamin Vials for Sterility Concerns

    Well Care Compounding Pharmacy is recalling 869 vials of Methylcobalamin 12.5mg/mL due to FDA inspection findings of GMP violations that may impact sterility.

    Product
    METHYLCOBALAMIN 12.5MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0974-2016·2016-06-15

    Aidarex Recalls Ceftriaxone for Injection Due to Manufacturing Deviations

    Aidarex Pharmaceuticals is recalling Ceftriaxone for Injection due to out-of-specification intermediates during manufacturing.

    Product
    CEFTRIAXONE for Injection USP, 250mg/vial, Rx only, MFG: LUPIN LIMITED INDIA, Packaged by Aidarex Pharmaceuticals, NDC 53217-0117-01
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0949-2016·2016-06-08

    Akorn Recalls Sulfacetamide Sodium Ophthalmic Solution Due to Sterility Concerns

    Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.

    Product
    Sulfacetamide Sodium Ophthalmic Solution, USP, 10%, Sterile, Rx Only, 15 mL bottles, Mfd. by: Akorn, Inc., Lake Forest, IL 60045 --- NDC 17478-221-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0910-2016·2016-06-08

    FDA Recalls Unapproved Ligandrol Supplements Sold Nationwide and in Brazil

    Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.

    Product
    LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0938-2016·2016-06-08

    Baptist Health Recalls TPN Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling seven bags of TPN 1 (amino acid 20%) in Arkansas due to a lack of sterility assurance.

    Product
    TPN 1, (amino acid 20%) 2000 ml bag (140), FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock Arkansas
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0945-2016·2016-06-08

    Baptist Health Recalls Vancomycin IV Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 88 bags of Vancomycin 1500 mg in 270 mL 0.9% NS due to a lack of sterility assurance.

    Product
    Vancomycin 1500 mg in 270 mL 0.9% NS bag, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0942-2016·2016-06-08

    Baptist Health Recalls Vancomycin IV Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 47 bags of Vancomycin 750 mg in 250 mL 0.9% NS due to a lack of sterility assurance.

    Product
    Vancomycin 750 mg in 250 mL 0.9% NS bag, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0931-2016·2016-06-08

    Baptist Health Recalls Nafcillin IV Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling seven bags of Nafcillin 3 grams in 277 mL 0.9% NS due to a lack of sterility assurance. The product was distributed in Arkansas.

    Product
    Nafcillin 3 grams in 277 mL 0.9% NS bag, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0946-2016·2016-06-08

    Baptist Health Recalls Vancomycin IV Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 54 bags of Vancomycin 1750 mg in 270 mL 0.9% NS due to a lack of sterility assurance. The product was distributed in Arkansas.

    Product
    Vancomycin 1750 mg in 270 mL 0.9% NS bag,FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0921-2016·2016-06-08

    Baptist Health Recalls Daptomycin Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 14 bags of Daptomycin 650 mg in 50 mL 0.9% NS due to a lack of sterility assurance.

    Product
    Daptomycin 650 mg in 50 mL 0.9% NS bag, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0919-2016·2016-06-08

    Baptist Health Recalls Clindamycin IV Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 16 bags of Clindamycin 900 mg in 100 mL 0.9% NS due to a lack of sterility assurance.

    Product
    Clindamycin 900 mg in 100 mL 0.9% NS bag, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0943-2016·2016-06-08

    Baptist Health Recalls Vancomycin IV Bags Due to Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 59 bags of Vancomycin 1000 mg in 250 mL 0.9% NS due to a lack of sterility assurance.

    Product
    Vancomycin 1000 mg in 250 mL 0.9% NS bag, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0912-2016·2016-06-08

    Baptist Health Pharmacy Recalls 1/2 Normal Saline Bags for Sterility Concerns

    Baptist Health Medical Towers Pharmacy is recalling 7 bags of 1/2 Normal Saline due to lack of sterility assurance. The product was distributed in Arkansas.

    Product
    1/2 Normal Saline 2000 mL + Sodium Acetate 80 mEq., FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
    Category
    Drug
    Distribution
    1 state