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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 2,181–2,200 of 18,034 recalls

FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Ultra 9150 Whey Protein Isolate. Product Code: 3232…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Ultra 8000 Nutritional Whey Protein Isolate. SKU 322…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Ultra 9100 Functional Whey Protein Isolate. SKU 3213…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Bravo 600 Functional Whey Protein SKU 32106. 34% Pr…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Bravo 550 Functional Whey Protein SKU 32105. 34% Pr…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Bravo 500 Functional Whey Protein SKU 32103. 34% Pr…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Bravo 300 Functional Whey Protein SKU 32102. 34% Pr…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Bravo 250 Functional Whey Protein SKU 32101. Grade…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Lactose. SKU 30601. Grade A. Refined Pasteurized.…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

GRANDE CHEESE COMPANY

Product
Grande Lactose SKU 30600. Grade A. Refined Pasteurized. N…
Reason
Possible Salmonella contamination.
Published
June 19, 2024
Distribution
AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States Terminated Historical recordClass I

Healthwest Minerals, Inc. dba Mt. Capra Products

Product
Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.)…
Reason
The Goat Milk Formula Recipe Kit has been sold and marketed as infant formula, but product has not submitted to FDA the premarket notification required for an infant formula for review.
Published
June 19, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

U.B.C. Food Distributors INC.

Product
Baraka brand ground black pepper packaged in 7oz retail cont…
Reason
Potential Salmonella contamination
Published
June 19, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Tivicay PD (dolutegravir) 5mg Tablets for Oral Suspension, 60-count bottles, Each carton contains one bottle of 60 tablets, one 30-mL dosing cup and one 10-mL oral dosing syringe, Rx Only, Mfd for: ViiV Healthcare Durham, NC, 27701, By: GlaxoSmithKline Durham, NC 27701, NDC 49702-255-37

by GlaxoSmithKline LLC

Reason
Labeling: Incorrect Lot and/or Expiration Date: The carton has incorrect expiration of 2026-MAY*, whereas the correct expiration date, which is on the tablet bottle label, is 2025-APR.
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Estradiol Transdermal System, USP (Twice-Weekly) 0.025mg/day, Rx Only, Manufactured by: Cadila Healthcare Limited, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1191-8

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Impurities/Degradation Specifications.
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Estradiol Transdermal System, USP (Twice-Weekly) 0.0375mg/day, Rx Only, Manufactured by: Cadila Healthcare Limited, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1192-8

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Impurities/Degradation Specifications.
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Pregabalin Capsules 50mg, 1000-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, Manufactured by: Laurus Labs Limited, Anakapalli-531011, India, NDC 64980-411-10

by Rising Pharma Holding, Inc.

Reason
Presence of Foreign Tablets/Capsules: Complaint received from a re-packager, American Health Packaging (AHP), where a foreign tablet was discovered in one of the bottles during packaging set up. Tablet identified as pantoprazole tablet 20mg.
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cephalexin for Oral Suspension, USP, 250mg/5mL, Rx only, 200mL (when mixed), Each contains cephalexin monohydrate, USP equivalent to 5g cephalexin. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9207-1.

by Bryant Ranch Prepack, Inc.

Reason
Labeling: Not Elsewhere Classified: Back Label states 'Each contains: cephalexin monohydrate, USP equivalent to 5g' instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 10g'
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cephalexin for Oral Suspension, USP, 250mg per 5mL, Rx only, 100mL (when mixed), Each contains cephalexin monohydrate, USP equivalent to 5g cephalexin. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9206-1.

by Bryant Ranch Prepack, Inc.

Reason
Labeling: Not Elsewhere Classified: Back Label states Each contains: cephalexin monohydrate, USP equivalent to 5g' on the back label instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 5g'
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cephalexin for Oral Suspension, USP, 250mg/ 5mL, Rx only, 200mL (when mixed), Each contains cephalexin monohydrate, USP equivalent to 5g cephalexin. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-8858-1.

by Bryant Ranch Prepack, Inc.

Reason
Labeling: Not Elsewhere Classified: Back Label states 'Each contains: cephalexin monohydrate, USP equivalent to 5g' instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 10g'
Published
June 12, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed), Each contains: cephalexin monohydrate, USP equivalent to 2.5g of cephalexin in a strawberry flavored mixture. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9205-1.

by Bryant Ranch Prepack, Inc.

Reason
Labeling: Not Elsewhere Classified: Back label states Each contains: cephalexin monohydrate, USP equivalent to 2.5g' instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 5g
Published
June 12, 2024
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.