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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
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 3,941–3,960 of 18,034 recalls

FDA Recall United States Completed Historical recordClass II

Bella Brands, LLC DBA Bella Cucina Artful Food

Product
Bella Cucina Artful Food Fresh Basil Pesto Net Wt. 3 oz (84.…
Reason
Label does not indicate milk on the label.
Published
November 9, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Completed Historical recordClass II

Bella Brands, LLC DBA Bella Cucina Artful Food

Product
Bella Cucina Artful Food Dried Cherry and Almond Biscotti Ne…
Reason
Label does not indicate milk and wheat on the label.
Published
November 9, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Completed Historical recordClass II

Bella Brands, LLC DBA Bella Cucina Artful Food

Product
Bella Cucina Artful Food Death By Chocolate Cookies Net Wt.…
Reason
Label does not indicate milk and wheat on the label.
Published
November 9, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Completed Historical recordClass II

Bella Brands, LLC DBA Bella Cucina Artful Food

Product
Bella Cucina Artful Food CROSTATA SWEET BUTTER PASTRY TARTS…
Reason
Label does not indicate milk on the label.
Published
November 9, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Completed Historical recordClass II

Bella Brands, LLC DBA Bella Cucina Artful Food

Product
Bella Cucina Artful Food Arugula & Pine Nut Pesto Net Wt. 6…
Reason
Label does not indicate milk on the label.
Published
November 9, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Completed Historical recordClass II

Bella Brands, LLC DBA Bella Cucina Artful Food

Product
Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 o…
Reason
Label does not indicate milk on the label.
Published
November 9, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.

by Exela Pharma Sciences LLC

Reason
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only, Manufactured and Distributed by: Exela Pharma Sciences, LLC Lenoir, NC 28645. Carton NDC 51754-5001-5, vial NDC 51754-5001-1

by Exela Pharma Sciences LLC

Reason
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg, 90 Tablets bottles Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520, Made in India, NDC 65862-162-90

by Aurobindo Pharma USA Inc.

Reason
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC 60429-027-10

by Golden State Medical Supply Inc.

Reason
Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Pyridostigmine Bromide Oral Solution, USP 60 mg/5 mL Delivers 5 mL, packaged in 5mL unit-dose cup, Rx only, Dist. by: VistaPharm, NDC 66689-406-01

by VistaPharm, Inc.

Reason
cGMP Deviations: Out of specification for assay of one of the preservative ingredients.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Green Tea and Aloe, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle, and c) 1.7 fl oz or 50 mL bottle, Supplier details: Ultra Chem Labs, Ontario, CA, Active Ingredients - Benzalkonium Chloride 0.13% (antimicrobial), ULS 8357 0.33% (antimicrobial shield), NDC 79208-001-50.

by Ultra Chem Labs Corp

Reason
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Odor Free, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle and c) 1.7 fl oz or 50 mL bottle, Supplier details: Ultra Chem Labs, Ontario, CA, Active Ingredients - Benzalkonium Chloride 0.13% (antimicrobial), ULS 8357 0.33% (antimicrobial shield), NDC 79208-001-50.

by Ultra Chem Labs Corp

Reason
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Fondaparinux Sodium Injection, USP, 7.5 mg per 0.6 mL, Single Dose, Prefilled Syringe, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520. Made in India. NDC 55150-232-10 (carton)NDC 55150-232-00 (syringe)

by AuroMedics Pharma LLC

Reason
Subpotent Drug: Out of specification for assay
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

The Chai Box

Product
THE CHAI BOX CHAI CONCENTRATE UNSWEETENED 16FL OZ/473ML glas…
Reason
Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 4.9.
Published
November 2, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

The Chai Box

Product
THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UP…
Reason
Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 4.9.
Published
November 2, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Secrets Of The Tribe

Product
Indian Gooseberry Alcohol-Free Extract, 2 oz. glass bottle,…
Reason
Product has elevated level of lead.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Secrets Of The Tribe

Product
Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376…
Reason
Product has elevated level of lead.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs, 1000mL Bag, 12 PK, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC 49230-300-10

by Fresenius Medical Care Holdings, Inc.

Reason
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Published
October 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough ACETAMINOPHEN/ PAIN RELIEVER DEXTROMETHORPHAN HBr/ COUGH SUPPRESSANT GUAIFENESIN/ EXPECTORANT PHENYLEPHRINE HCl/ NASAL DECONGESTANT Maximum Strength Decongestant Free DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015 walgreens.com

by LNK International, Inc.

Reason
Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Published
October 26, 2022
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.