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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 October 2026.

37,269
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 1,521–1,540 of 17,287 recalls

FDA Recall United States TerminatedTerminated: July 22, 2025Historical recordClass I

Wismettac Asian Foods, Inc.

Product
Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK,…
Reason
Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: July 22, 2025Historical recordClass I

Wismettac Asian Foods, Inc.

Product
Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK,…
Reason
Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Made Good Variety Pack 37ct 2.MadeGood Variety Pack 7ct
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1.Chocolate Drizzled Vanilla Granola Bars 25.5oz (30 bars) 2…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1.Holiday Sprinkles Chocolate Drizzled Granola Mini Bars 10…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Chocolate Drizzled Cookie Crumble Granola Bars 4.2oz (5 b…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Chocolate Drizzled Birthday Cake Granola Bars 25.5oz (30…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Halloween Chocolate Chip Granola Mini Bars 12.6oz (30 bar…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Cookies & Creme Granola Bars 30.6oz (36 bars) 2. Cookies…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Strawberry Granola Bars 30.6oz (36 bars) 2. Strawberry Gr…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Mixed Berry Granola Bars; 34oz (40 bars) 2. Mixed Berry G…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. Chocolate Banana Granola Bars; 5.1oz (6 bars) 2. Chocolat…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
Chocolate Chip Granola Mini Bars, 0.42oz
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Riverside Natural Foods, Ltd.

Product
1. MadeGood Chocolate Chip Granola Bars 34oz (40 bars) 2. M…
Reason
may contain metal pieces
Published
February 19, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01

by ENDO USA, Inc.

Reason
Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin¿ (epinephrine injection, USP)
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters), Rx Only, Distributed by: Aurobindo Pharma USA< INC., 279 Princeton-Hightstown Road, East Windsor, NJ 08520. Made in India. Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152. NDC: 0904-7216-61

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason
Failed Dissolution Specifications.
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

HydrALAZINE Hydrochloride, 100 Tablets (10x10), USP, 50mg, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-328-10

by SKY PACKAGING

Reason
Failed Impurities/Degradation Specifications
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10

by SKY PACKAGING

Reason
Failed Impurities/Degradation Specifications
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, NDC 63459-910-11, Blister NDC 63459-910-12; (b)10 syringes in 1 CARTON, NDC 63459-910-15, Blister NDC 63459-910-12; (c) 1 syringe in 1 CARTON, NDC 63459-910-17 without safety guard and blister, Rx Only, Manufactured by: UAB Teva Baltics, Vilnius, Lithuania. Distributed by Teva Pharmaceuticals USA, Inc. North Wales PA 19454. Product of Israel.

by Teva Pharmaceuticals USA, Inc

Reason
Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Carvedilol Tablets, USP, 12.5 mg, Rx only, a)500 Tablets, NDC 68462-164-05; b) 100 Tablets, NDC 68462-164-01, Manufactured for Glenmark Pharmaceuticals, NJ.

by Glenmark Pharmaceuticals Inc., USA

Reason
CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit.
Published
February 12, 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.