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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.

37,062
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 1,561–1,580 of 21,559 recalls

FDA Recall Ongoing Historical recordClass II

Chlorthalidone Tablets, USP, 25 mg, 50 Tablets (5x10) Unit Dose cards per carton, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 50268-167-15

by AvKARE

Reason
Failed Dissolution Specifications
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Celecoxib Capsules, 200 mg, 50 Capsules (5x10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 50268-169-15

by AvKARE

Reason
Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division), Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-142-71

by Alembic Pharmaceuticals Limited

Reason
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
HKBKF04 1/11.25 OZ. EA Created Fresh Breakfast Bowl-Southwes…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Ki…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
RTSALSA1LB 1# EAST COAST FRESH Salsa Cup - 1 lb ALL LOT CODE…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
HKSAN169 1/5.76OZ CREATED FRESH Sub- Egg Salad on Everything…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
HKSAN167 1/5.76 OZ. EA CREATED FRESH Sub- Tuna Salad on Ever…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
HKSAC168 6/5.76 OZ. CS CREATED FRESH Sub- Chicken Salad on E…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
5185 2/7.125# EAST COAST FRESH AUTHENTIC GREEK SALAD (4070 2…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass I

Sysco Corporation

Product
3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT…
Reason
Cucumbers have the potential to be contaminated with Salmonella
Published
June 18, 2025
Distribution
DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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FDA Recall United States Terminated Historical recordClass III

NOW Foods

Product
NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 024…
Reason
regular yeast was inadvertently packaged as nutritional yeast
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y8…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLB…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D72…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sweetheart USA, LLC

Product
Gluten Free Vegan Peanut Butter Jam Cookie, Net Wt. 3.5 oz (…
Reason
Undeclared sesame
Published
June 18, 2025
Distribution
Distributed to 11 restaurants in Ohio

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FDA Recall Ongoing Historical recordClass II

Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: 53329-202-08, UPC 8 88277 34945 5

by Consumer Product Partners, LLC

Reason
Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
Published
June 11, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4

by Apotex Corp.

Reason
Defective Container: This recall is being initiated due to a leaking unit stored horizontally.
Published
June 11, 2025
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.