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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,450
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 14,961–14,980 of 21,307 recalls

FDA Recall United States TerminatedTerminated: September 28, 2017Historical recordClass I

Dawn Food Products Inc.

Product
R&H CHOCOLATE Speedy Creme Instant Pudding and Pie Filling…
Reason
Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published
April 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 28, 2017Historical recordClass I

Dawn Food Products Inc.

Product
R&H Speedy Creme Vanilla Filling Mix Item 01148908 25 pou…
Reason
Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published
April 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 28, 2017Historical recordClass I

Dawn Food Products Inc.

Product
R&H VANILLA Speedy Creme Instant Pudding and Pie Filling Mi…
Reason
Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published
April 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 28, 2017Historical recordClass I

Dawn Food Products Inc.

Product
QUIK 'N CREAMY VANILLA POWDERED FILLING Item number 000141…
Reason
Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published
April 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
Ultimate Amish SAmpler Box Containing packages of Guggisberg…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
Taste of Goodness Basket Containing packages of Guggisberg M…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
Holiday Delight Box Containing packages of Guggisberg Colby…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
Holiday Crowd Pleaser Basket Containing packages Guggisberg…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
Custom Gift Box Containing various packages of Guggisberg Ch…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG Country Christmas Basket Containing packages of…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG Cheese Lover's Box Containing packages of Colby,…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG NATURAL CHEESE THUNDER JACK INGREDIENTS: Pasteuri…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG NATURAL CHEESE PEPPER JACK INGREDIENTS: Pasteuriz…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG FARMERS CHEESE INGREDIENTS: Pasteurized Part Skim…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG NATURAL CHEESE MARBLE INGREDIENTS: Pasteurized Mi…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Dutch Valley Food Distributors

Product
GUGGISBERG NATURAL CHEESE COLBY INGREDIENTS: Pasteurized Mil…
Reason
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Published
April 26, 2017
Distribution
Producct was shipped to the following st…

View recall →

FDA Recall TerminatedTerminated: April 17, 2017Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, packaged in a) 60-count bottles (NDC 59746-317-60) and b) 100-count bottles (NDC 59746-317-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 17, 2017Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, packaged in a) 60-count bottles (NDC 59746-316-60) and b) 100-count bottles (NDC 59746-316-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published
April 19, 2017
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 17, 2017Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 100 mg, packaged in a) 60-count bottles (NDC 59746-315-60) and b) 100-count bottles (NDC 59746-315-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published
April 19, 2017
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 19, 2024Historical recordClass II

hydrALAZINE HYDROCHLORIDE INJECTION, USP, 20 mg/mL, 1 mL Single Dose Vial, packaged in 25 Vials per carton, Rx only, APP Fresenius Kabi USA, LLC, Lake Surich, IL 60047, NDC 63323-614-01, Distributed by McKesson Medical-Surgical, Inc.

by Mckesson Medical Surgical

Reason
Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.
Published
April 19, 2017
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.

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