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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 6,661–6,680 of 17,327 recalls

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Ja…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Springboard Green Power, Dietary Supplement; 240g Plastic B…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
RAWr! Life Organic Superfoods; Dietary Supplement; 300g Pla…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
L.O.V.E. Supermeal Vanilla Chai: 1320g Plastic Bottle, 660…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
L.O.V.E. Supermeal Original: 420g Plastic Bottle, 1396g Pla…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Purim Daily Fiber Blend - Original unflavored; 540g Plastic…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Daily Fiber Blend - Caramel Apple Flavor; Organic Plant Pow…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Nested Naturals Super Kids; Superfood Powder Full of Nutrie…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Erom, Inc. Slim Natural Raw Meal; Bulk; Finished product i…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
care/of Chia/Flax Boost Dietary Supplement; Net Wt. 0.35 oz…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Alkamind Creamy Vanilla Organic Daily Protein; 450g Plastic…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Alkamind Creamy Chocolate Organic Daily Protein; 450g Plast…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg, 90 count bottle, Rx Only, Manufactured by Jubilant Generics Ltd, Roorkee-247661 India, NDC 59746-284-90

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
CGMP Deviations: Presence of dark brown discoloration on edges of tablets
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Solifenacin Succinate Tablets, 10 mg, packaged in a) 30-count bottles (NDC 51991-894-33) and b) 90-count bottles (NDC 51991-894-90), Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487; Manufactured by: Piramal Enterprises Limited Plot No 67-70, Sector -2 Pithampur 454 775, Dist, Dhar Madhya Pradesh, INDIA

by Breckenridge Pharmaceutical, Inc

Reason
CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might convert to Solifenacin Tartrate Tablets.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Solifenacin Succinate Tablets, 5mg, packaged in a) 30-count bottles (NDC 51991-893-33) and b) 90-count bottles (NDC 51991-893-90) Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487; Manufactured by: Piramal Enterprises Limited Plot No 67-70, Sector -2 Pithampur 454 775, Dist, Dhar Madhya Pradesh, INDIA

by Breckenridge Pharmaceutical, Inc

Reason
CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might convert to Solifenacin Tartrate Tablets.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Atorvastatin Calcium Tablets, USP 40 mg, Rx only, 500-count bottle, Manufactured by: Sun Pharmaceutical Industries Limited Mohali, INDIA, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 63304-829-05

by Sun Pharmaceutical Industries, Inc.

Reason
Presence of foreign substance: Foreign matter has been identified as latex glove in one lot of Atorvastatin Calcium Tablets USP 40 mg.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) patches, Delivers 15 mg over 9 hours (1.6 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5553-3

by Noven Therapeutics, LLC

Reason
Defective Delivery System: Out of specification for mechanical peel and shear.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.

by Med Man Distribution, Inc.

Reason
Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-01; NDC Berkley Jensen: 68391-852-56; NDC: CVS Health: 59779-540-01; NDC DG Health: 55910-011-01; NDC Kirkland: 63981-852-56; NDC Kroger: 30142-600-56; NDC Meijer: 41250-852-01; NDC Rite Aid: 11822-0852-4; NDC Walgreens: 0363-0852-01

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate: 49035-800-75; NDC Up & Up: 11673-950-75

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
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.