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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.

37,061
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 1,481–1,500 of 22,291 recalls

FDA Recall Ongoing Historical recordClass II

Doxepin Hydrochloride Capsules, USP, 10 mg, 100 Capsules, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panela v 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-637-31

by Alembic Pharmaceuticals Limited

Reason
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 60mg, 1,000-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-748-10.

by Breckenridge Pharmaceutical, Inc.

Reason
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

King Cheesecake Company, Inc.

Product
Item #2485 Assorted layer cake
Reason
Pecans have the potential to be contaminated with Salmonella
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

King Cheesecake Company, Inc.

Product
Item #99273 chocolate Tres Leches Cheesecake
Reason
Pecans have the potential to be contaminated with Salmonella
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

King Cheesecake Company, Inc.

Product
Item #3145 Hummingbird Layer Cake
Reason
Pecans have the potential to be contaminated with Salmonella
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

King Cheesecake Company, Inc.

Product
Item #99272 Tres Leches Cheesecake
Reason
Pecans have the potential to be contaminated with Salmonella
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

King Cheesecake Company, Inc.

Product
Item #1312 Carrot layer cake
Reason
Pecans have the potential to be contaminated with Salmonella
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

King Cheesecake Company, Inc.

Product
Item #1071 Italian layer cake
Reason
Pecans have the potential to be contaminated with Salmonella
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass I

Doehler North America, Inc.

Product
Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.3…
Reason
Listeria monocytogenes. During routine testing the firm received positive test results for Listeria monocytogenes.
Published
August 13, 2025
Distribution
Product was shipped to the following: Di…

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FDA Recall United States Terminated Historical recordClass III

Cesarina Bakery, Inc

Product
SESAME SEED COOKIES Cesarina Cookies, Net Weight. 16 oz. (45…
Reason
Allergen not listed in the Contains statement: Sesame
Published
August 13, 2025
Distribution
Product was distributed in FL, GA, NC

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FDA Recall United States Terminated Historical recordClass II

Cesarina Bakery, Inc

Product
MEDITERRANEAN MIX COOKIES, Cesarina Cookies, Net Weight. 16…
Reason
Allergen not listed in the Contains statement: Sesame
Published
August 13, 2025
Distribution
Product was distributed in FL, GA, NC

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FDA Recall United States Terminated Historical recordClass I

Krasnyi Oktyabr USA Inc

Product
ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH…
Reason
Clostridium botulinum (uneviscerated fish)
Published
August 13, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Inte…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended u…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Inte…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton, Rx Only, Manufactured by: Hikma Berkeley Heights, NJ 07922, NDC# 0641-6044-25

by Hikma Pharmaceuticals USA Inc.

Reason
Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Sucralfate Tablets, USP 1 gram, packaged in a) 100-count bottles NDC 29033-0003-01, and b) 500-count bottles, NDC 29033-0003-05), Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120.

by Nostrum Laboratories, Inc.

Reason
CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets 90 mg, 30-count bottles, Rx only, Manufactured by: Strides Pharma Science Ltd. Puducherry, India; Distributed by: Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-885-04

by Strides Pharma, Inc.

Reason
Failed Dissolution Specifications.
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04

by Pfizer Inc.

Reason
CGMP Deviations; particulates identified during visual inspection
Published
August 6, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10, Syringe NDC - 60793-701-02

by Pfizer Inc.

Reason
CGMP Deviations; particulates identified during visual inspection
Published
August 6, 2025
Distribution
Nationwide

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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.