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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
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 2,921–2,940 of 21,324 recalls

FDA Recall Terminated Historical recordClass I

Atovaquone Oral Suspension USP, 750 mg per 5 mL sachets, 20 Units x 5 mL cartons, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 50268-086-12.

by AvKARE

Reason
Microbial contamination of a non-sterile product: potential Bacillus cereus contamination.
Published
April 24, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial packed 25 vials per carton, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor, NJ 08520, NDC 55150-223-10

by Eugia US LLC

Reason
Presence of Particulate Matter
Published
April 17, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054. Blister Pack NDC 0591-2436-45, Carton NDC 0591-2436-15

by Teva Pharmaceuticals USA, Inc

Reason
Superpotent Drug: The 3-month stability result for assay was found to be above specification limit
Published
April 17, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41

by NATCO Pharma Limited

Reason
CGMP Deviations
Published
April 17, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06

by Lupin Pharmaceuticals Inc.

Reason
Subpotent Drug
Published
April 17, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lidl US TRADING

Product
Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g…
Reason
Undeclared Wheat, Soy, Egg, Milk, Tree Nuts (foreign language labeling)
Published
April 17, 2024
Distribution
Imported product directly shipped to a w…

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FDA Recall United States Terminated Historical recordClass I

Backstage Center DBA CTC Seller

Product
Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35…
Reason
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Published
April 17, 2024
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES SWEET POTATO CASSEROLE CONTAINS: EGG, MILK PIES…
Reason
During an inspection by NCDA, the firm was notified that the product label fails to list any ingredients.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILL…
Reason
During an inspection by NCDA, the firm was notified that the product label fails to list any sub ingredients.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES SQUASH CASSEROLE CONTAINS: MILK, EGGS, SOY, FIS…
Reason
During an inspection by NCDA, the firm was notified that the product label fails to list any ingredients.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass I

Robeson Enterprises

Product
PIES & SIDES PUMPKIN PIE 10.5 oz INGREDIENTS: PUMPKIN FILLIN…
Reason
During an inspection by NCDA, the firm was notified that the product contains undeclared milk and eggs. The label fails to list any sub ingredients and the contain statement does not list milk or eggs.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES DOT'S POTATO BAKE 2lb INGREDIENTS: IDAHO POTATO…
Reason
During an inspection by NCDA, the firm was notified that the label fails to list any sub ingredients.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES PEACH PIE INGREDIENTS: PEACH PIE FILLING, SUGAR…
Reason
During an inspection by NCDA, the firm was notified that the label fails list any sub ingredients.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass I

Robeson Enterprises

Product
PIES & SIDES MO' MONEY PIE INGREDIENTS: BLACK EYED PEAS, COL…
Reason
During an inspection by NCDA, the firm was notified that the label fails to declare the allergen soy as an ingredient. The firm was also notified that the label does not list any sub ingredients or the allergen soy in the contains statement.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass I

Robeson Enterprises

Product
PIES & SIDES BAKED MAC AND CHEESE, ALLERGENS: MILK, PIES & S…
Reason
During an inspection by NCDA, the firm was notified that the label fails to declare the allergen egg as an ingredient or in the allergen statement. The firm was also notified that the label does not list any of the ingredients for their product.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES HASHBROWN CASSEROLE, ALLERGENS: MILK, WHEAT, SO…
Reason
During an inspection by NCDA, the firm was notified that the label does not list the ingredients for their products.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES GREEN BEAN CASSEROLE, CONTAINS: MILK, SOY, FISH…
Reason
During an inspection by NCDA, the firm was notified that the label does not list the ingredients for their products.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass I

Robeson Enterprises

Product
PIES & SIDES DEEP SOUTH TOMATO PIE, INGREDIENTS: SLICED TOMA…
Reason
The firm was notified that the label did not list any sub ingredients. The product contains pimento cheese which is made with mayonnaise which may include eggs. Undeclared eggs.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES CONNIE'S CARAMEL APPLE PIE 11 oz INGREDIENTS: A…
Reason
During an inspection by NCDA, the firm was notified that the label does not list the sub ingredients for their products.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES CHERRY PIE INGREDIENTS: CHERRY PIE FILLING, SUG…
Reason
During an inspection by NCDA, the firm was notified that the label does not list the sub ingredients for their products.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

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.