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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 4,321–4,340 of 17,299 recalls

FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product
Plant Based Yogurt Culina Bourbon Vanilla Nt Wt 5 oz. (142 g…
Reason
Potential for glass to be found in product
Published
July 13, 2022
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product
Plant Based Yogurt Culina Blueberry Lavender Nt Wt 5 oz. (14…
Reason
Potential for glass to be found in product
Published
July 13, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Prairie City Bakery

Product
Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey…
Reason
Salmonella. Product contains recalled Jif peanut butter as ingredient.
Published
July 13, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16

by Akorn, Inc.

Reason
Defective container: defect prevents product from dispensing as intended.
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02

by Akorn, Inc.

Reason
Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186. NDC 68968-5552-3

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc. Camarillo, CA 93012, NDC 61152-199-99, UPC 7 69682 29101 3

by Green Pharmaceuticals, Inc.

Reason
Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC # 33342-052-44, Rx Only, MFR: Macleods Pharma USA, Inc. Plainsboro, NJ 08536

by Macleods Pharma Usa Inc

Reason
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles, Rx Only, Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-165-90 UPC 3 72789 16590 5

by PD-Rx Pharmaceuticals, Inc.

Reason
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-164-90 UPC 3 72789 16490 8

by PD-Rx Pharmaceuticals, Inc.

Reason
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP 25 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-163-90 UPC 3 72789 16390 1

by PD-Rx Pharmaceuticals, Inc.

Reason
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Industries Inc

Product
Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 71…
Reason
Milk contamination
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Industries Inc

Product
Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 71…
Reason
Milk contamination
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. W…
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER FUDGE BAR (24-8OZ) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
VARIETY TRAY (16 OZ) (C-CNC-PBC) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz.
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
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.