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Recall totals

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

37,139

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 25, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Litehouse Inc

Product: OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per…
Reason: OPA by Litehouse Ranch was recalled due to undeclared egg.
Published: September 13, 2017
Distribution: distributed in CA, CO, IA, ND, NE, OR, a…

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FDA Recall Terminated Historical recordClass II

Morphine Sulfate Oral Solution, 100 mg/ 5 mL (20 mg/mL), packaged in a 1 oz. bottle containing 30 mL with an oral syringe, Rx Only, Manufactured by: Tris Pharma, Inc. Monmouth Junction, NJ 08852, NDC 27808-082-01

by Tris Pharma Inc.

Reason: Defective container: Oral solution leaking from container.
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted) bottle, Rx Only, Manufactured By: Cipla Ltd. at Medispray Laboratories Pvt. Ltd., Kundaim Goa, India; Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054, NDC 60432-065-00.

by Morton Grove Pharmaceuticals, Inc.

Reason: Presence of Foreign Substance: customer complaint of blue foreign material identified as a portion of a nitrile glove was discovered in product.
Published: September 6, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product: Amrita Pineapple Chia Energy Bar, 50gm UPC: 853009004025
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 Apricot Strawberry Protein Bar, 50gm 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 I

Amrita Health Foods

Product: Amrita Chocolate Chip Coconut 15g Protein Bar, 60gm UPC: 85…
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 Sunflower Butter & Jelly 15g Protein Bar, 60gm UPC:…
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 Dark Chocolate Quinoa 15g Protein Bar, 60gm UPC: 853…
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 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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Data last updated: September 25, 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.