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Recall totals

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

37,118

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 20, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product: Amrita Cranberry Raisin Energy Bar, 50gm UPC: 853009004032
Reason: Product may be contaminated with Listeria monocytogenes
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product: Amrita Apple Cinnamon Energy Bar, 50gm UPC: 853009004049
Reason: Product may be contaminated with Listeria monocytogenes
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product: Amrita Mango Coconut Energy Bar, 50gm UPC: 853009004018
Reason: Product may be contaminated with Listeria monocytogenes
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product: Amrita Chocolate Maca 15g Protein Bar, 60 gm UPC: 853009004…
Reason: Product may be contaminated with Listeria monocytogenes
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Garden Of Light Inc.

Product: (a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch,…
Reason: Product labeled containing pecans actually contains almonds
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KIND, LLC

Product: 4-count boxes of KIND Breakfast Dark Chocolate Cocoa Bars…
Reason: Mislabeled Outer Box labeled as : KIND Breakfast Dark Chocolate Cocoa Bars may contain KIND Breakfast PROTEIN Dark Chocolate Cocoa Bars.
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

GRANDE PRODUCE LTD CO

Product: Caribena yellow maradol papaya packed in 35 pound cases
Reason: Product is contaminated with Salmonella
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, ?Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59

by The Harvard Drug Group

Reason: Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47

by The Harvard Drug Group

Reason: Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09

by The Harvard Drug Group

Reason: Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150. NDC: 0536-1001-85

by The Harvard Drug Group

Reason: Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85

by The Harvard Drug Group

Reason: Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count bottle (NDC 55289-791-21), d) 30-count bottle (NDC 55289-791-30), e) 60-count bottle (NDC 55289-791-60), Packaged by PD-Rx Pharmaceuticals, Incorporated, Oklahoma City, OK. 73127 Mfg: KVK-Tech, Inc. Newtown, PA 18940

by PD-Rx Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10

by C. O. Truxton

Reason: Labeling: Label Mixup; potentially mislabeled
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amitriptyline HCL Tablets, USP 50 mg, 100 count bottles, Rx Only, Manufactured for: Qualitest Pharmaceuticals Huntsville, AL 35811, Distributed by: Truxton, Inc. Bellmawr, NJ 08031, NDC: 0463-6352-10

by C. O. Truxton

Reason: Labeling: Label Mixup; potentially mislabeled
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031

by C. O. Truxton

Reason: Labeling: Label Mixup; potentially mislabeled
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phenobarbital Tablets USP, 60 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6151-10

by C. O. Truxton

Reason: Labeling: Label Mixup; potentially mislabeled
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10

by C. O. Truxton

Reason: Labeling: Label Mixup; potentially mislabeled
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10

by C. O. Truxton

Reason: Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets
Published: August 30, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Grandma's Herbs

Product: "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Die…
Reason: Grandmas Herbs Cholesterol has undeclared soy lecithin.
Published: August 30, 2017
Distribution: Nationwide

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Data last updated: September 20, 2026 ET

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.