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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.

37,269
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 821–840 of 22,402 recalls

FDA Recall United States TerminatedTerminated: July 21, 20262026 recordClass III

Super World Trading Inc.

Product
MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz…
Reason
Products contain cyclamates (banned sweetener)
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: April 16, 20262026 recordClass II

TG FOODS INC

Product
Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Po…
Reason
The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: April 16, 20262026 recordClass III

Pocas International Corp.

Product
POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA 12 X 13.8OZ
Reason
Packaging integrity issue that may compromise product quality .
Published
April 8, 2026
Distribution
The product was distributed to the follo…

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FDA Recall United States TerminatedTerminated: April 16, 20262026 recordClass III

Pocas International Corp.

Product
POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA 12 X 13.8OZ
Reason
Packaging integrity issue that may compromise product quality .
Published
April 8, 2026
Distribution
The product was distributed to the follo…

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FDA Recall United States TerminatedTerminated: April 16, 20262026 recordClass III

Pocas International Corp.

Product
POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ
Reason
Packaging integrity issue that may compromise product quality .
Published
April 8, 2026
Distribution
The product was distributed to the follo…

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FDA Recall United States TerminatedTerminated: April 16, 20262026 recordClass III

Pocas International Corp.

Product
POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ
Reason
Packaging integrity issue that may compromise product quality .
Published
April 8, 2026
Distribution
The product was distributed to the follo…

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FDA Recall Ongoing2026 recordClass II

Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.

by Amerisource Health Services LLC

Reason
Failed tablet specifications.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9262-08.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9259-08.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 10 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9257-08.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44

by MACLEODS PHARMA USA, INC

Reason
Subpotent Drug
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.

by Chiesi USA, Inc.

Reason
Lack of Assurance of Sterility
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass III

Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35

by Radnostix

Reason
Failed Tablet/Capsule Specifications
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing2026 recordClass II

South Florida Food, LLC

Product
Pan de Bono (Cheese Bread), 100 units per Paper Cardboard Bo…
Reason
Undeclared Soy.
Published
April 1, 2026
Distribution
Products distribute in FL

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FDA Recall United States Ongoing2026 recordClass II

Bakkavor

Product
Roasted Tomato Parmesan Focaccia Bread sold under the brand…
Reason
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Published
April 1, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing2026 recordClass II

Bakkavor

Product
Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8…
Reason
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Published
April 1, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: May 11, 20262026 recordClass II

Savannah Bee Company Inc.

Product
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (4…
Reason
Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the product inside the bottle is a different flavor of BBQ sauce. After investigation, the firm determined that the product in the bottle is their Honey BBQ Sauce "Sweet". The BBQ sauce "Sweet" contains wheat and soy which is not listed on the BBQ Sauce "Mustard" label.
Published
April 1, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: May 8, 20262026 recordClass II

American Laboratories, LLC

Product
Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American La…
Reason
Potential Salmonella contamination.
Published
April 1, 2026
Distribution
11 direct wholesale accounts located in…

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FDA Recall United States TerminatedTerminated: May 8, 20262026 recordClass II

American Laboratories, LLC

Product
Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American…
Reason
Potential Salmonella contamination.
Published
April 1, 2026
Distribution
11 direct wholesale accounts located in…

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FDA Recall United States TerminatedTerminated: May 8, 20262026 recordClass II

American Laboratories, LLC

Product
Pepsin Full Strength Powder, 50 kg, Item #5000545, American…
Reason
Potential Salmonella contamination.
Published
April 1, 2026
Distribution
11 direct wholesale accounts located in…

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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.