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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.

37,061
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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 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 2,161–2,180 of 18,528 recalls

FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Coffee + Non-Dairy Creamer + Sugar + Pumpkin Spice Syrup Can…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Coffee + Non-Dairy Creamer + Caramel Syrup Canned Beverage p…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Coffee + Non-Dairy Creamer + Maple Syrup Canned Beverage pac…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Coffee + Non-Dairy Creamer + Sugar + Coconut Syrup Canned Be…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Coffee + Non-Dairy Creamer + Sugar-Free Sweetener Canned Bev…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Coffee + Non-Dairy Creamer + Sugar Canned Beverage packaged…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee + Maple Syrup Canned Beverage packaged under th…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee + Vanilla Syrup Canned Beverage packaged under…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee + Sweet Syrup Canned Beverage packaged under th…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee + Chocolate Syrup and Sugar Canned Beverage pac…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee + Chocolate Syrup Canned Beverage packaged unde…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee + Sugar Canned Beverage packaged under the foll…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Snapchill, LLC

Product
Black Coffee Canned Beverage packaged under the following br…
Reason
Potential under-processing.
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Diflorasone Diacetate Ointment, USP, 0.05%, 60g tube, Rx only, Mfd. By: Lyne Laboratories, Inc., Brockton, MA 02301; Mfd. For: Rising Pharmaceuticals, Inc., East Brunswick, NJ 08816 NDC 64980-124-60

by Rising Pharma Holding, Inc.

Reason
Failed Impurities/Degradation Specifications: The impurity results at 12 months stability testing,did not conform to the specification limit.
Published
July 17, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, NDC 16714-301-01 (vial), NDC 16714-301-10 (outer box).

by Zydus Pharmaceuticals (USA) Inc

Reason
Cross contamination with other products
Published
July 17, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1725-01 (vial), NDC 70710-1725-06 (outer box).

by Zydus Pharmaceuticals (USA) Inc

Reason
Cross contamination with other products
Published
July 17, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2

by Tailstorm Health INC

Reason
Subpotent Drug: reduced efficacy for epinephrine
Published
July 17, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534, Vial NDC: 70710-1644-1, Carton NDC: 70710-1644-5.

by Zydus Pharmaceuticals (USA) Inc

Reason
Cross contamination with other products.
Published
July 17, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Verapamil Hydrochloride Injection, USP 5 mg / 2mL(2.5 mg/mL), packaged as (a) 25x2 mL Single-Dose Vial per carton, Vial NDC: 70710-1643-1; Carton NDC 70710-1643-7; (b) 5x2 mL Single-Dose Vial per carton, Vial NDC: 70710-1643-1; Carton NDC 70710-1643-5; Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534,

by Zydus Pharmaceuticals (USA) Inc

Reason
Cross contamination with other products.
Published
July 17, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Blemfree All Day Lotion (salicylic acid 0.5% w/w), packaged in a) 1 oz. 29 ML tube NDC:53228-003-01 b) 4 OZ 118ML plastic bottle, UPC 7 01450 90008 6, NDC # 53228-002-01, Equibal Labs, Inc

by Equibal Inc

Reason
CGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
Published
July 17, 2024
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.