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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

16876–16900 of 18009

  • 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.)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-800-2013·2013-07-24

    Arm & Hammer Sodium Bicarbonate Powder Recalled for 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, Sodium Bicarbonate U.S.P. No. 4 Granular, Net Wt. 50 lbs. (22.68 kg.) per bag, Manufactured by: Church & Dwight Co., Inc., 469 N. Harrison St., Princeton, N.J. 08543-5297, Product #60411.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-797-2013·2013-07-24

    Arm & Hammer Sodium Bicarbonate Powder Recalled for 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) USP1 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. 1 Powdered, Net Wt. 50 lbs. (22.68 kg.) per bag…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-802-2013·2013-07-24

    Quetiapine Fumarate Tablets Recalled for Failed Dissolution Test

    American Health Packaging is recalling Quetiapine Fumarate 25mg tablets because they failed a dissolution test during stability studies.

    Product
    QUETIAPINE Fumarate Tablets 25mg 100 Tablets (10x10) Blister card, Rx, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 68084-530-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-807-2013·2013-07-24

    Bayer Recalls Medroxyprogesterone Acetate API Due to Stability Failures

    Bayer HealthCare Pharmaceuticals Inc. is recalling 194.62 kg of Medroxyprogesterone acetate API because it failed stability specifications for particle size.

    Product
    Medroxyprogesterone acetate, micronized (EP, USP) active pharmaceutical ingredient, Rx only, packaged in 6.0 kg drums (labeled as 6,000 kg), Bayer Schering Pharma AG, D-13342 Berlin
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-764-2013·2013-07-17

    Olympia Pharmacy Recalls Oxytocin Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Oxytocin 20 units/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Oxytocin 20 units/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-759-2013·2013-07-17

    Olympia Pharmacy Recalls Metoclopramide Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Metoclopramide 5 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Metoclopramide 5 mg/ml Injection,compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-718-2013·2013-07-17

    Olympia Pharmacy Recalls Detomidine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Detomidine w/Xylazine Injection due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Detomidine w/Xylazine 100 mg/mg Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-740-2013·2013-07-17

    FDA Recalls Compounded HCG Injections Due to Sterility Concerns

    Olympia Pharmacy is recalling compounded HCG injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    HCG 125iu/0.25ml (550iu/ml), 3500iu and 10,000iu, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-783-2013·2013-07-17

    Olympia Pharmacy Recalls Stanozolol Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Stanozolol injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Stanozolol (50 mg/ml and 100 mg/ml) Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-786-2013·2013-07-17

    Olympia Pharmacy Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Testosterone Cypionate injections because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Testosterone Cypionate (100 mg/ml & 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-755-2013·2013-07-17

    Olympia Pharmacy Recalls Methylcobalamin Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Methylcobalamin P 10/ml Creatine 40 mg/ml / Arginine 100 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Methylcobalamin P 10/ml Creatine 40 mg/ml / Arginine 100 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-753-2013·2013-07-17

    Olympia Pharmacy Recalls Metabolase Forte Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Metabolase Forte Injection because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Metabolase Forte Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-795-2013·2013-07-17

    Olympia Pharmacy Recalls Xylazine Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Xylazine 300 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Xylazine 300 mg/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-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-791-2013·2013-07-17

    Olympia Pharmacy Recalls Compounded Vitamin B12 Injections Due to Sterility Concerns

    Olympia Pharmacy is recalling compounded Vitamin B12 injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Vitamin B12 (3000 mcg/ml & 5000 mcg/ml) 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-773-2013·2013-07-17

    Olympia Pharmacy Recalls Polidocanol Injections Due to Sterility Concerns

    Olympia Pharmacy is recalling Polidocanol injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Polidocanol (0.75%, 1%, 3%, and 10%) 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-735-2013·2013-07-17

    Gentamicin Sulfate Injection Recalled for Sterility Concerns

    Olympia Pharmacy is recalling Gentamicin Sulfate 80 mg/ml Injection due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Gentamicin Sulfate 80 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide