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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,501–12,520 of 17,237 recalls

FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Yellow Cake Mix; NET WT 20 z. (1 lb 4oz) 567 g); UPC…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

J&D's Down Home Enterprises, Inc.

Product
Original Bacon Flavored Seasoning Salt, Big Pig brand, 16oz…
Reason
Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a potential to be contaminated with E. coli O121.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product
Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. 3…
Reason
Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product
IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb.…
Reason
Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 1…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product
Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 g) I…
Reason
Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST White Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Hydrocortisone and acetic acid otic solution, Rx only, 10 mL bottle, Distributed by Actavis Inc. 60 Columbia Road Bldg B. Morristown, NJ 07560 USA , NDC 45963-412-61

by Actavis Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature sample(s).
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Acetasol HC (hydrocortisone and acetic acid otic solution USP) , Rx Only, 10 mL bottle, Manufactured by: Actavis Midatlantic LLC 1877 Kawai Road Lincolnton, NJ 28092 USA, NDC 0472-0882-82

by Actavis Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature sample(s).
Published
August 31, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Amoxicillin for Oral Suspension USP, 400 mg/ 5 mL, 50 mL bottle, Rx only, Manufactured In Canada by: Teva Canada Limited, Toronto, Canada, NDC 0093-4161-76

by Teva North America

Reason
Superpotent drug: Out of specification test result for assay during stability testing.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.

by Akorn, Inc.

Reason
Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 10 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-452-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-452-56; and c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-452-19; Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason
CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 5 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-451-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-451-56, c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-451-19; and d) 30-count tablets per dosage card in a carton, NDC 51079-451-69, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason
CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 2.5 mg*, packaged in a)100-count (10 x 10) unit dose blisters per carton, NDC 51079-450-20 and b) 30-count tablets per dosage card in a carton, NDC 51079-450-63, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason
CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published
August 31, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Urea (50% Urea in a Cream Base), a) Net Wt. 5 oz (142 g), (NDC 42808-0200-05) b) Net Wt. 9 oz (225 g) (NDC 42808-0200-09), Rx Only, Manufactured in the U.S.A. for Exact-Rx Inc., Melville, NY

by Exact-Rx Inc

Reason
Crystallization; complaints received by the manufacturer of crystals forming in product
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Remeven Cream, (50% Urea in a Cream Base), a) 5.0 oz (142 g) and b) 9.0 oz (255 g) tubes, Rx only, Manufactured by Sonar Products Inc, Carlstadt, NJ. Distributed by Stratus Pharmaceuticals Inc., Miami, FL.

by Stratus Pharmaceuticals Inc

Reason
Crystallization; Complaints that cream appears to have crystallized
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection, 12 mg, 10 ml depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247

by Talon Compounding Pharmacy

Reason
Lack of Assurance of Sterility
Published
August 31, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Human Chorionic Gonadotropin Injection (a) 2500 iu, (b) 2500 iu with B12, (c) 3500 iu, (d) 5000 iu, (e) 5000 iu with B12, (f) 6000 iu, (g) 7500 iu, (h) 7500 iu with B12, (i)11,000 iu, (j)11,000 iu with B12, (k) 15,000 iu, (l) 20,000 iu, (m) 20,000 iu with B12, 10 mL sterile, depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247

by Talon Compounding Pharmacy

Reason
Lack of Assurance of Sterility
Published
August 31, 2016
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.