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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 3,621–3,640 of 18,346 recalls

FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Pingo Peanut Butter Cookie Hot Chocolate packaged in single…
Reason
Coffee pods may contain undeclared peanut residue
Published
March 22, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single…
Reason
Coffee pods may contain undeclared peanut residue
Published
March 22, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Mead Johnson & Company

Product
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
Reason
Reckitt, a producer of nutrition products, announced today that out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii.
Published
March 22, 2023
Distribution
AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI,…

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product
Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.…
Reason
Undeclared peanut allergen
Published
March 22, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product
Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.)…
Reason
Undeclared peanut allergen
Published
March 22, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product
Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection p…
Reason
Coffee pods may contain undeclared peanut residue
Published
March 22, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Purely Soothing MSM Nasal Spray, 15%, packaged in 30ml, 1.014 fl. oz bottles, Manufactured by: Pharmedica USA, Phoenix, AZ, UPC 7 31034 91380 5

by Pharmedica USA, LLC

Reason
CGMP Deviations
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.

by Pharmedica USA, LLC

Reason
Non-Sterility
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.

by Nanomaterials Discovery Corporation

Reason
Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

by Akron Pharma, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%), packaged in 1 oz. (28.3g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz, liquid oral rinse plastic bottles, Manufactured for: All USA Direct LLC, Broadview, IL 60155

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Nose Better Gel (0.75% Camphor, 0.50% Menthol, 0.50% Allantoin), packaged in 0.46 oz. (13g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Soltice Quick-RUB (Menthol 5.1%, Camphor 5.1%) packaged in a) 1.33 oz (37g) plastic jars and b) 3 Oz (85g) plastic jars

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Unguentine Original Ointment for Burns (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%) packaged in 1 oz. (28g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Vencedor medicated balm (capsaicin 0.028%) 1.5 oz. (43g) tubes, Distributed by: The Larkspur Group Inc. Norwalk, CT 06854

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Alcolado Relampago (menthol 1%, camphor 1.5%), packaged in a) 7 fluid oz. (207 ml) and b) 16 fluid oz. (472 ml) bottles, Distributed by: The Larkspur Group Inc. South Norwalk, CT 06854

by Ecometics, Inc.

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health 13796 Compark Blvd Englewood CO 80112, NDC 71449-148-94

by Denver Solutions, LLC DBA Leiters Health

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag, Leiter Compounding Health 13796 Compark Blvd Englewood CO 80112, NDC 71449-150-82

by Denver Solutions, LLC DBA Leiters Health

Reason
CGMP DEVIATIONS
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes, Rx only, Leiters 13796 Compark Blvd Englewood CO 80112, NDC 71449-001-15

by Denver Solutions, LLC DBA Leiters Health

Reason
CGMP DEVIATIONS
Published
March 15, 2023
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.