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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 October 2026.

37,341
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 8,381–8,400 of 17,454 recalls

FDA Recall TerminatedTerminated: August 16, 2022Historical recordClass II

Testosterone Cypionate Injection, USP, 1000 mg/10 mL (100 mg/mL), For intramuscular use only, 10 mL Vial, Multiple-Dose, Rx Only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-536-37.

by InvaGen Pharmaceuticals, Inc.

Reason
Presence of Particulate Matter.
Published
April 24, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 16, 2022Historical recordClass II

Testosterone Cypionate Injection, USP, 200 mg/mL, For IM use only, 1 mL Vial, Single Dose, Rx Only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-537-31.

by InvaGen Pharmaceuticals, Inc.

Reason
Presence of Particulate Matter.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 16, 2022Historical recordClass II

Testosterone Cypionate Injection, USP, 2000 mg/10 mL (200 mg/mL), For intramuscular use only, 10 mL Vial, Multiple-Dose, Rx Only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-537-37.

by InvaGen Pharmaceuticals, Inc.

Reason
Presence of Particulate Matter.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: October 19, 2020Historical recordClass II

ConAgra Foods, INc.

Product
Hunts Tomato Paste No Salt Added 6 ounce cans, 12 per whole…
Reason
Mold. This situation is due to potential damage to the cans.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass III

Wholesome Treats, Inc.

Product
Breads from Anna Classic Herb Bread Mix 19oz, carton
Reason
Undeclared flaxseed. Flaxseed was used in the products but is not listed on the product labels.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass III

Wholesome Treats, Inc.

Product
Breads from Anna Dairy & Corn Free Bread Mix 19oz, carton
Reason
Undeclared flaxseed. Flaxseed was used in the products but is not listed on the product labels.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass III

Wholesome Treats, Inc.

Product
Breads from Anna Yeast Free Bread Mix 18.1oz, carton
Reason
Undeclared flaxseed. Flaxseed was used in the products but is not listed on the product labels.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass III

Wholesome Treats, Inc.

Product
Breads from Anna Banana Bread Mix 14oz, carton
Reason
Undeclared flaxseed. Flaxseed was used in the products but is not listed on the product labels.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass III

Wholesome Treats, Inc.

Product
Breads from Anna Black Bean Brownie Mix 14oz, carton
Reason
Undeclared flaxseed. Flaxseed was used in the products but is not listed on the product labels.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: January 10, 2024Historical recordClass I

LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1 Sachet 15 gr / 0.53 Oz is labeled as LEOPARD Miracle of Honey, UPC 8 699415 912859, Manufactured in Turkey, www leopardhoneytr.com.

by USA LESS Inc.

Reason
Marketed Without An Approved NDA/ANDA: product tainted with undeclared sildenafil, an FDA approved drug for the treatment of male erectile dysfunction. The presence of sildenafil in Leopard Miracle Honey renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published
April 17, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 6, 2020Historical recordClass III

Thallous Chloride TI 201 Injection, Specific Concentration: 37 MBq/mL (1 mCi/mL), Total Activity: 325.6 MBq (8.8 mCi) Volume: 8.8 mL vial, Rx Only, Mfg. by GE Healthcare, Medi-physics, Inc., Arlington Heights, IL 60004. NDC: 17156-299-18

by Medi-Physics Inc. dba GE Healthcare

Reason
Chemical Contamination: Trace amounts of an impurity was detected in the reagent used to manufacture finished product.
Published
April 17, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 14, 2020Historical recordClass II

Pravastatin Sodium Tablets USP, 20 mg, 500-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot No. 2, Phase-2, Pharma zone SEZ, Pithampur, Dist-Dhar, Madhya Pradesh 454 775, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430. NDC 68462-196-05

by Glenmark Pharmaceuticals Inc., USA

Reason
Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.
Published
April 17, 2019
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/25mg, a) 30-count (NDC: 13668-118-30), b) 90-count (NDC: 13668-118-90), c) 1000-count (NDC: 13668-118-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published
April 17, 2019
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/12.5mg, a) 30-count (NDC: 13668-117-30), b) 90-count (NDC: 13668-117-90) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published
April 17, 2019
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Losartan Potassium / Hydrochlorothiazide Tablets, USP 50mg/12.5mg, a) 30-count (NDC: 13668-116-30), b) 90-count (NDC: 13668-116-90), c) 1000-count (NDC: 13668-116-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published
April 17, 2019
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 90-count (NDC: 13668-115-90), b) 1000-count (NDC: 13668-115-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published
April 17, 2019
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count (NDC: 13668-409-30), b) 90-count (NDC: 13668-409-90), c) 1000-count (NDC: 13668-409-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published
April 17, 2019
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b) 1000-count (NDC: 13668-113-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking Ridge, NJ

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level.
Published
April 17, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: May 23, 2022Historical recordClass II

Gavilyte-N, PEG-3350, Sodium chloride, Sodium Bicarbonate and Potassium Chloride for Oral Solution, Rx only, Manufactured by Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, MD NDC 43386-050-19 UPC 343386050192 a) Lemon Flavor Pack net wt. 2 g UPC 343386200023 b) Orange Flavor Pack net wt. 2 g UPC 343386202027 c) Cherry Flavor Pack net wt. 2 g UPC 3433862034

by LUPIN SOMERSET

Reason
Labeling Not Elsewhere Classified; orange and cherry flavor packets incorrect list "natural lemon flavor" as an ingredient
Published
April 17, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: December 15, 2020Historical recordClass II

Life-Line tm Catalytic Activated Energy Water, 1 gallon container, McDaniel Life-Line LLC 1775 US Hwy 385 806-647-1741 Dimmitt, TX 79027

by McDaniel Life-Line LLC

Reason
Unapproved new drug
Published
April 17, 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.

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