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 deaths or serious injuries are reported, 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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11076–11100 of 11860

  • SevereFDA (Drugs)·D-805-2013·2013-07-24

    Sandoz Recalls Estarylla Contraceptive Tablets Due to Placebo Tablet Error

    Sandoz Incorporated is recalling Estarylla tablets because a placebo tablet was found in a row of active tablets, which could reduce contraceptive effectiveness.

    Product
    Estarylla (Norgestimate and Ethinyl Estradiol) Tablets. USP, 0.25mg/0.035mg, 3X28 tablets per carton. Rx only, Manufactured by Laboratorios Leon Farma S.A. Spain for Sandoz Inc. Princeton, NJ 08540, NDC 0781-4058-15
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-798-2013·2013-07-24

    Arm & Hammer Sodium Bicarbonate Powder Recalled for Foreign Substance Contamination

    Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.

    Product
    Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP2 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 469 N. Harrison St., Princeton, NJ 08543-5297; and b) Sodium Bicarbonate U.S.P. No. 2 Fine Granular, Net Wt. 50 lbs. (22.68 kg.) per
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-801-2013·2013-07-24

    Arm & Hammer Sodium Bicarbonate Powder Recalled for Foreign Substance Contamination

    Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.

    Product
    Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP5 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 469 N. Harrison St., Princeton, NJ 08543-5297; and b) Sodium Bicarbonate U.S.P. No. 5 Coarse Granular, Net Wt. 50 lbs. (22.68 kg.) pe
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-723-2013·2013-07-17

    Olympia Pharmacy Recalls Diphenhydramine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Diphenhydramine 50 mg/ml Injection because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Diphenhydramine 50 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-738-2013·2013-07-17

    Olympia Pharmacy Recalls Guanabenz Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Guanabenz 20 mg/ml Injection because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Guanabenz 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-751-013·2013-07-17

    Olympia Pharmacy Recalls Medroxyprogesterone Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Medroxyprogesterone 150 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Medroxyprogesterone 150 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-761-2013·2013-07-17

    Olympia Pharmacy Recalls Miconazole Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Miconazole 3% Injection because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Miconazole 3% Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-700-2013·2013-07-17

    Olympia Pharmacy Recalls Aminophylline Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Aminophylline 2.5% Injection because FDA inspection findings raised concerns about quality control processes and assurance of sterility.

    Product
    Aminophylline 2.5% Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-693-2013·2013-07-17

    Olympia Pharmacy Recalls Acepromazine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Acepromazine 25 mg/ml Injection because FDA inspection findings raised concerns about quality control processes and assurance of sterility.

    Product
    Acepromazine 25 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-765-2013·2013-07-17

    Olympia Pharmacy Recalls Papaverine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling six vials of Papaverine 40 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Papaverine 40 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-793-2013·2013-07-17

    Olympia Pharmacy Recalls Vitamin B-Buildup Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Vitamin B-Buildup Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Vitamin B-Buildup Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-737-2013·2013-07-17

    Olympia Pharmacy Recalls Compounded Guanabenz Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling three vials of compounded Guanabenz 8 mg/ml Injection due to FDA inspection findings regarding quality control and sterility assurance.

    Product
    Guanabenz 8 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-782-2013·2013-07-17

    Olympia Pharmacy Recalls Sodium Tetradecyl Sulfate Injections Due to Sterility Concerns

    Olympia Pharmacy is recalling specific lots of compounded Sodium Tetradecyl Sulfate injections due to FDA inspection findings regarding quality control and sterility assurance.

    Product
    Sodium Tetradecyl Sulfate (0.125%, 1%, 2.5%, 3%, and 4%) Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-750-2013·2013-07-17

    Olympia Pharmacy Recalls Medetomidine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Medetomidine 2 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Medetomidine 2 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-796-2013·2013-07-17

    Olympia Pharmacy Recalls Yohimbine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Yohimbine 10 mg/ml Injection because FDA inspection findings raised concerns about quality control and assurance of sterility.

    Product
    Yohimbine 10 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-757-2013·2013-07-17

    Olympia Pharmacy Recalls Methylcobalamin Injections Due to Sterility Concerns

    Olympia Pharmacy is recalling two lots of compounded Methylcobalamin injections nationwide and in Puerto Rico due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Methylcobalamin 25 mg/ml Inj and 5000 mcg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-767-2013·2013-07-17

    Olympia Pharmacy Recalls Pento-Gluc Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Pento-Gluc 200 mg/ml Injection due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Pento-Gluc 200 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-788-2013·2013-07-17

    Olympia Pharmacy Recalls Tripelennamine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling two lots of compounded Tripelennamine 20 mg/ml Injection due to FDA inspection findings regarding quality control and sterility assurance.

    Product
    Tripelennamine 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-685-2013·2013-07-17

    Fresenius Kabi Recalls Benztropine Mesylate Injection Due to Glass Particulates

    Fresenius Kabi is recalling 65,110 vials of Benztropine Mesylate Injection due to the presence of glass particulate matter. The affected vials were distributed nationwide and in Puerto Rico.

    Product
    BENZTROPINE MESYLATE — BENZTROPINE MESYLATE (BENZTROPINE MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-695-2013·2013-07-17

    Olympia Pharmacy Recalls Alprostadil Due to Sterility Concerns

    Olympia Pharmacy is recalling Alprostadil 2000 mcg/ml because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Alprostadil 2000 mcg/ml, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-768-2013·2013-07-17

    Olympia Pharmacy Recalls Pentosan Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling three vials of compounded Pentosan 250 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Pentosan 250 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-715-2013·2013-07-17

    Cre-O-Pan Injection Recalled Due to Sterility Concerns

    Olympia Pharmacy is recalling Cre-O-Pan Injection because FDA inspection findings raised concerns about quality control processes and assurance of sterility.

    Product
    Cre-O-Pan Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-714-2013·2013-07-17

    Olympia Pharmacy Recalls Clenbuterol Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Clenbuterol 0.03mg/ml Injection because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Clenbuterol 0.03mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-724-2013·2013-07-17

    Olympia Pharmacy Recalls Disodium EDTA Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Disodium EDTA Injection because FDA inspection findings raised concerns about quality control processes and assurance of sterility.

    Product
    Disodium EDTA Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-712-2013·2013-07-17

    Olympia Pharmacy Recalls Ceftiofur Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Ceftiofur GM vials because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Ceftiofur GM vial 50 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide