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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,116
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls
Most common hazardLack of Assurance of Sterility 2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potatoPublished September 16, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 8,541–8,560 of 18,020 recalls

FDA Recall Terminated Historical recordClass II

Nandrolone Decanoate 200 mg/mL Injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lipo MIC-12 (Methylcobalamin, USP 1mg, Methionine USP 15mg, Inositol, FCC 50mg, Choline Chloride, FCC 100 mg) 10 mL Injectable vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ipamorelin Acetate 9 mg/9mL Injectable vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Human Chorionic Gonadotropin 12,000 IU vials Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Human Chorionic Gonadotropin 5,000 IU vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Human Chorionic Gonadotropin 10,000 IU vials, Rx only Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

B-complex (Thiamine 100mg, Riboflavin 2mg, Niacinamide 100 mg, Pyridoxine 2mg, Depanthenol 5mg) injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846, NDC 69699-1611-30

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Bacteriostatic Water for Injection, 10 mL vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846

by Pharm D Solutions, LLC

Reason
Lack of Sterility Assurance.
Published
June 19, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Izzio Artisan Bakery, LLC

Product
Izzio Artisan Bakery 100% Rye Bread, Net Weight: 9 oz ; 8 s…
Reason
100% Rye Bread may contain undeclared wheat.
Published
June 19, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

LAIRD SUPERFOOD INC

Product
Performance Mushrooms product is dried mushroom blend of 4 d…
Reason
The product is incorrectly labeled with 14 mg of Iron and 78% DV when the actual amount is 14 mcg of Iron and 0% DV.
Published
June 19, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Icco Cheese Co Inc

Product
Gia Russa Whole Grain Italian Seasoned Bread Crumbs in 10 Oz…
Reason
Product contains undeclared Allergens: Walnuts & Pecans
Published
June 12, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Icco Cheese Co Inc

Product
Gia Russa Whole Grain Italian Unseasoned Bread Crumbs in 10…
Reason
Product contains undeclared Allergens: Walnuts & Pecans
Published
June 12, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules per packet.

by Stiff Boy LLC

Reason
Marketed without an Approved NDA/ANDA: The Beast contains undeclared sildenafil which was discovered through FDA analysis.
Published
June 5, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Cefdinir for Oral Suspension USP, 250mg/5mL, Powder for oral suspension, 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 20201, Manufactured by: Lupin Limited, Mandideep 462 046 India. NDC 68180-723-20

by Lupin Pharmaceuticals Inc.

Reason
Complaint received of metal piece identified in the product bottle prior to the reconstitution.
Published
June 5, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Unison Hand Care Products, WHITE PEARLIZED Anti-Bacterial Hand Cleaner with Triclosan, #4302, with exclusive Bajan fragrance, packaged in 800 ML (27 FL OZ) pouch containers, 12-800 ml containers/12-27 FL. OZ. container pouches per case, National Chemical Laboratories, Inc., 401 North 10th Street, Philadelphia, PA 19123.

by Inopak Ltd

Reason
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Published
June 5, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Antibacterial Hand Soap, .3% P.C.M.X, labeled as STYLE Antibacterial Hand Soap with moisturizers, a) 1000 ml pouches, 10/1000 ML. Large Valve pouches per case, 5031-404-LN, b) 1000 ml pouches, 8/1000 ML. Disc Pumps pouches per case, 5031-L1000, c) 800 ML Universal Valve pouches, 12/800 ML Universal Valve pouches per case, 5031-404, d) 800 ml pouches, 12/800 ML Presspak pouches per case, "B", 5031-403-1B, e) 800 ml pouches, 12 x 800ML. KC Valve pouches per case, 5031-404-KC, f) 800 ml pouches, 12/800 ML Universal Valve pouches per case, 5031-404, g) 800 ml pouches, 12/800 ML Presspak pouches per case, "B", 5031-403-1B, h) 500 ml pouches, 6/500 ML. KC Valve pouches per case, 5031-404-500-6, i) 500 ml pouches, 18/500 ML. KC Valve pouches per case, 5031-404-500, j) 500 ml pouches, 6/500 ML. KC Valve pouches per case, 5031-404-500-6, k) 8 oz. bottles, 24/8 OZ. bottles with pumps per case, 5031-440-03, l) 18 oz. bottles, 16 x 18 OZ. Bottles with Pumps per case, 5031-430-02, m) 1000 ml pouches, 10/1000 ML. Large Valve pouches per case, 5031-404-LN, n) 1000 ml pouches, 8/1000ML. Disc Pumps pouches per case, 5031-L1000; Choice Antibacterial Hand Soap, packaged as o) 800 ml/27fl.oz. pouches, 12/800 ml Universal Valve pouches per case, 5031-404UV-CH, Manufactured by Inopak LTD., Ringwood, NJ.

by Inopak Ltd

Reason
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Published
June 5, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Sani-Guard-SF Waterless Foam Hand Sanitizer, Ethyl Alcohol 70%, packaged in a) 6/1000 ml pouches per case, 5068-FL1000, b) 1000 ml cartridge pouch, 6/1000 ml .8ml Option Cartridge pouches per case, 5068-OS1000, Inopak LTD

by Inopak Ltd

Reason
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Published
June 5, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Mild Health Care Antibacterial Hand Soap, .6% P.C.M.X., packaged in a) 1000 ml Disc Pump pouches, 8 x 1000 ml Disc Pump pouches per case, 5013-L1000, b) 2000 ml. Disc Pump pouches, 4 x 2000 ml Disc Pump pouches per case, 5013-XL2000, c) 800 ml Universal Valve pouches, 12 x 800 ml Universal Valve pouches per case, 5013-404, d) 1 gallon bottles, 4/1 gallon bottles per case, 5013-420-02, INOPAK, LTD., 24 Executive Parkway, Ringwood, NJ 07456.

by Inopak Ltd

Reason
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Published
June 5, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Antibacterial Hand Soap, Healthcare 2000, labeled as a) DERMA System CARE SaniClenz Antimicrobial Skin Cleanser (Chlorhexidine Gluconate), 4 x (1 gallon containers), Reorder/REF #JSCG; Manufactured for Crosstex International, Inc.; b) MEDI-WASH CHG Anti-Microbial Hand Wash with Chlorhexidine Gluconate; 1000ML pouches, 8/1000ML pouches per case, Walter G. Legge Co Inc, 444 Central AVE, Peekskill, NY 10566

by Inopak Ltd

Reason
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Published
June 5, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

INOFOAM Foaming E-2 Food Handling Wash with .6% PCMX, 1000mL pouch (NDC 058575-110-11), 6/1000 ML pouches per case (NDC 058575-110-80), 5064-FL1000, Inopak, LTD.

by Inopak Ltd

Reason
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Published
June 5, 2019
Distribution
Nationwide

View recall →

Data last updated:

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.