Skip to main content
Get Alerts

Data Explorer

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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 2,621–2,640 of 20,481 recalls

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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 →

FDA Recall United States Ongoing Historical recordClass III

Robeson Enterprises

Product
PIES & SIDES Broccoli Casserole Contains: Wheat, Eggs, Milk,…
Reason
During an inspection by NCDA, the firm was notified that the label does not list any ingredients in the product.
Published
April 17, 2024
Distribution
Products were shipped to the following s…

View recall →

FDA Recall United States Terminated Historical recordClass II

Whitley Peanut Factory, Inc.

Product
Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Elect…
Reason
Undeclared Allergen (peanuts, milk, soy, wheat, and sesame).
Published
April 17, 2024
Distribution
The recalled product was distributed to…

View recall →

FDA Recall Terminated Historical recordClass III

Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After Reconstitution: For direct intravenous injection or must be further diluted before intravenous infusion, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc., Big Flats, NY 14814, NDC # 39822-0255-01.

by X-Gen Pharmaceuticals Inc.

Reason
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
Published
April 10, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized, Cytotoxic Agent, Single Dose Vial for Intravenous Use, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc. Big Flats, NY 14814, NDC # 39822-0250-01.

by X-Gen Pharmaceuticals Inc.

Reason
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
Published
April 10, 2024
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-6030-1

by IntegraDose Compounding Services LLC

Reason
Lack of Assurance of Sterility: leaking bags
Published
April 10, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00

by B. Braun Medical Inc

Reason
Lack of assurance of sterility: bags have the potential to leak..
Published
April 10, 2024
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ, 07430, Product of India, NDC 68462-562-01

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
Published
April 10, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product
Powerade Mountain Berry Blast - 20oz PET bottles 24 vari…
Reason
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Published
April 10, 2024
Distribution
U.S. distribution to 760 consignees in S…

View recall →

FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product
Powerade Zero Fruit Punch - 20oz PET bottles 24 variety p…
Reason
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Published
April 10, 2024
Distribution
U.S. distribution to 760 consignees in S…

View recall →

FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product
Powerade Zero Mixed Berry - 20 oz PET bottles 24 variety pac…
Reason
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Published
April 10, 2024
Distribution
U.S. distribution to 760 consignees in S…

View recall →

FDA Recall Ongoing Historical recordClass I

Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01

by Par Sterile Products LLC

Reason
Presence of Particulate Matter.
Published
April 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Tri-Lo-Sprintec (norgestimate and ethinyl estradiol) tablets USP - triphasic regimen, packaged in carton containing 3 Blister Cards, 28 Tablets Each, Rx only, Teva Pharmaceuticals USA, INC, North Wales, PA 19454, NDC 0093-2140-62

by Teva Pharmaceuticals USA, Inc

Reason
Failed Dissolution Specifications
Published
April 3, 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.