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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12626–12650 of 18028

  • HighFDA (Drugs)·D-0545-2016·2016-01-06

    Walgreens Recalls Insulin Syringes Due to Sterility Assurance Concerns

    Walgreens Infusion Services is recalling 23 insulin syringes in Texas due to a lack of assurance of sterility.

    Product
    Insulin Regular (Human) syringe, a)15 unit/0.15 mL, b) 24 unit/0.24mL syringe, c) 50 unit/0.5 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0538-2016·2016-01-06

    Walgreens Recalls Milrinone Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling 19 bags of Milrinone 0.375 mcg/kg/min D5W in Texas due to a lack of assurance of sterility.

    Product
    Milrinone 0.375 mcg/kg/min D5W bag a) 365 mL, b) 400 mL c) 430 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0551-2016·2016-01-06

    Walgreens Recalls Nafcillin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling 7 bags of Nafcillin 12 gm in NS 500 mL due to a lack of assurance of sterility. The product was distributed in Texas.

    Product
    Nafcillin 12 gm in NS 500 mL bag, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0554-2016·2016-01-06

    Walgreens Recalls Cefepime Infusion Minibags Due to Sterility Concerns

    Walgreens Infusion Services is recalling 26 minibags of Cefepime 1 g/NS 100 mL due to a lack of assurance of sterility. The product was distributed in Texas.

    Product
    Cefepime 1 g/NS 100 mL Minibag Plus, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0527-2016·2016-01-06

    Walgreens Recalls Heparin Injection Syringes Due to Sterility Concerns

    Walgreens Infusion Services is recalling 49 syringes of Heparin injection, Preservative Free, due to a lack of assurance of sterility. The affected products were distributed in Texas.

    Product
    Heparin injection, Preservative Free, a) 280 units/0.28 mL, b) 350 units/0.35 mL syringe, c) 440 units/0.44 mL, d) 500 units/0.5 mL syringe, e) Heparin 800 units/0.8 f) Heparin 2300 units/2.3 mL syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0546-2016·2016-01-06

    Walgreens Recalls Famotidine Injection Syringes Due to Sterility Concerns

    Walgreens Infusion Services is recalling 21 famotidine injection syringes compounded by Option Care 148 in Texas due to a lack of assurance of sterility.

    Product
    Famotidine injection syringe a) 10 mg/1 mL b) 80 mg/8 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0529-2016·2016-01-06

    Walgreens Recalls Piperacillin/Tazobactam Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling 26 bags of Piperacillin/Tazobactam (Zosyn) Accuflo in Texas due to a lack of assurance of sterility.

    Product
    Piperacillin/Tazobactam (Zosyn) Accuflo bag, a) 18 g/NS 275 mL b) 4.5 g/NS 100 mL Accuflo, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0543-2016·2016-01-06

    Walgreens Recalls Folic Acid Syringes Due to Sterility Concerns

    Walgreens Infusion Services is recalling 23 folic acid syringes compounded in Texas due to a lack of assurance of sterility.

    Product
    Folic Acid 1 mg/0.2 mL syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0559-2016·2016-01-06

    PD-Rx Recalls Clonidine Hydrochloride Tablets Due to cGMP Deviations

    PD-Rx Pharmaceuticals is recalling 9 bottles of Clonidine Hydrochloride Tablets, 0.1 mg, distributed in Alabama due to cGMP deviations.

    Product
    Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottles, Rx only, Packaged by PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, MFG: Mutual Pharm. Co. Inc., Philadelphia, PA 19124, NDC 43063-509-01
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0477-2016·2015-12-30

    Dental Dressing Recall for Missing Drug Component Percentages

    Rainbow Specialty & Health Products is recalling Dressit-X dental dressings because the labeling does not list the percentage of drug components.

    Product
    Dressit-X, Radiopaque D-545, NDC 11004-545-40, Dental Use Only, Active Ingredients: Eugenol Oil
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0525-2016·2015-12-30

    Perrigo Recalls Equaline All Day Allergy Tablets Due to Impurity

    Perrigo is recalling Equaline All Day Allergy tablets because they contain an impurity called cetirizine monosaccharide ester.

    Product
    EQUALINE ALL DAY ALLERGY — EQUALINE ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0521-2016·2015-12-23

    Teva Recalls Irbesartan and Hydrochlorothiazide Tablets Due to Labeling Errors

    Teva Pharmaceutical Industries is recalling 3,536 bottles of Irbesartan and Hydrochlorothiazide tablets because some bottles have incorrect or missing lot and expiration dates.

    Product
    IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0511-2016·2015-12-16

    RemedyRepack Recalls Humulin 70/30 Vials Due to Incorrect Storage Instructions

    RemedyRepack, Inc. is recalling 65 vials of Humulin 70/30 insulin due to incorrect storage instructions on the label.

    Product
    Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0520-2016·2015-12-16

    Pfizer Recalls Norpace CR Capsules for Failed Dissolution Specification

    Pfizer is recalling Norpace CR (disopyramide phosphate) capsules because they failed to meet dissolution specifications. The recall covers specific lots distributed nationwide.

    Product
    NORPACE CR — NORPACE CR (DISOPYRAMIDE PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0514-2016·2015-12-16

    RemedyRepack Recalls Ascorbic Acid Injection Due to Incorrect Storage Instructions

    RemedyRepack Inc. is recalling Ascorbic Acid 500 MG/ML Injection vials because they contain incorrect storage instructions on the label.

    Product
    Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0512-2016·2015-12-16

    RemedyRepack Recalls Bicillin L-A Due to Incorrect Storage Instructions

    RemedyRepack, Inc. is recalling 60 vials of Bicillin L-A 600,000 Units/mL injection because the product labels contain incorrect storage instructions.

    Product
    Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0513-2016·2015-12-16

    RemedyRepack Recalls Vitamin B-Complex Injections Due to Labeling Error

    RemedyRepack Inc. is recalling Vitamin B-Complex 100 injections because the vials contain incorrect storage instructions.

    Product
    Vitamin B-Complex 100, Multi MG Inj, Qty: 30 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0873-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0518-2016·2015-12-16

    Steris Recalls Kindest Kare Antimicrobial Foaming Handwash Due to Labeling Error

    Steris is recalling 54 bottles of Kindest Kare Antimicrobial Foaming Handwash because an outdated label incorrectly lists an inactive ingredient.

    Product
    Kindest Kare Antimicrobial Foaming Handwash, Hand Soap, 0.75% Triclosan, 444 ml (15 fl oz) bottles, STERIS Corporation, 7501 Page Avenue, St. Louis, MO 63133, Reorder # 1452-RF, NDC 0519-1452-13, UPC (01)00724995 086251.
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0515-2016·2015-12-16

    RemedyRepack Recalls Lorazepam Injections Due to Incorrect Storage Instructions

    RemedyRepack Inc. is recalling 1,625 vials of Lorazepam 2 mg/mL injection because the product labels contain incorrect storage instructions.

    Product
    Lorazepam 2 mg/mL Inj., Qty: 1 mL Vial, MFG by: West-Ward Pharma, Eatontown, NJ 07724, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0316-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0516-2016·2015-12-16

    RemedyRepack Recalls Novolin 70/30 Vials Due to Incorrect Storage Instructions

    RemedyRepack Inc. is recalling 106 vials of Novolin 70/30 insulin because the packaging contains incorrect storage instructions.

    Product
    Novolin 70/30, 100 Units/mL Solu., Qty: 1 Vial, MFG by: Novo Nordisk, A/S, Bagsvaerd, Denmark DK-2880, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0414-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0517-2016·2015-12-16

    RemedyRepack Recalls Rocuronium Bromide Vials Due to Incorrect Storage Instructions

    RemedyRepack Inc. is recalling Rocuronium Bromide 50 mg/5 mL vials because the product labels contain incorrect storage instructions.

    Product
    Rocuronium Bromide 50 MG/5ML INJ., Qty: 5 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0222-57
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0509-2016·2015-12-16

    Golden State Medical Supply Recalls Meclizine Hydrochloride Tablets Due to Impurities

    Golden State Medical Supply Inc. is recalling 1,136 bottles of Meclizine Hydrochloride tablets because they failed impurity specifications.

    Product
    MECLIZINE HYDROCHLORIDE TABLETS, 12.5 mg, Packaged in 1000 ct Bottles, Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012. NDC: 60429-204-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0510-2016·2015-12-16

    Golden State Medical Supply Recalls Meclizine Hydrochloride Tablets for Impurities

    Golden State Medical Supply Inc. is recalling Meclizine Hydrochloride 25 mg tablets because they failed impurity specifications.

    Product
    MECLIZINE HYDROCHLORIDE TABLETS, 25 mg, Packaged in a) 100 ct Bottles (NDC: 60429-205-01) and b) 1000 ct Bottles (NDC: 60429-205-10), Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012.
    Category
    Drug
    Distribution
    Distributed nationwide