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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 5,481–5,500 of 17,299 recalls

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip The Big Cookie Cake Cookie cakes: 1LB…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip The Funfetti Cookie Cake Cookie cakes:…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Funfetti Cookies: Cookies: 4 oz / 114…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Peanutbutter Spice Cookies: 4 oz / 114…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Octoberfest Cookies: 4 oz / 114 grams…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Hot Chip Summer Cookies: 4 oz / 114 gr…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip The Disco Ball Cookies: 4 oz / 114 gra…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Fluffadoodle and Fluffa-Nutta Cookies:…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Maple Macadamia Cookies: 4 oz / 114 g…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Spiced Rum Oatmeal Raisin Cookies: 4 o…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip Spiced Oatmeal Raisin Cookies: 4 oz /…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip The Sweetie Cookies: 4 oz / 114 grams…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product
Chocolate & the Chip The Original Cookies: 4 oz / 114 grams…
Reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published
October 27, 2021
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285; Glucagon, NDC: 0002-8031-01

by Eli Lilly & Company

Reason
SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
Published
October 20, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride Extended-Release Tablets, USP 10 mEq (750 mg), 500 Tablets, Rx Only, Manufactured by: Strides Shasun Limited, Bengaluru - 562106, India, Distributed by: Strides Pharma In., East Brunswick, NJ 08816, NDC 64380-861-07.

by Strides Pharma Inc.

Reason
Failed Dissolution Specifications
Published
October 20, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Betaxolol Ophthalmic Solution, USP, 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL dropper bottle, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Carton NDC: 17478-705-10, Bottle NDC 17478-705-11

by Akorn, Inc.

Reason
Microbial Contamination of Sterile Products: Confirmed sterility failure identified during stability testing at the 12-month time point.
Published
October 13, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Firvanq (vancomycin hydrochloride for oral solution), Vancomycin 50 mg/mL Kit, Each Kit Includes: 1 bottle containing 7.7 g Vancomycin Hydrochloride USP, powder for oral solution and 1 bottle containing 145 mL Grape Flavored Diluent for reconstitution per carton, Rx only, Manufactured for: Azurity pharmaceuticals, Wilmington, MA 01887, NDC 65628-206-05.

by Azurity Pharmaceuticals, Inc.

Reason
Product Mix-up: Incorrect diluent component included in the kit.
Published
October 13, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Artesunate for Injection, 110 mg/vial, packaged in a) 2x2 pack containing 2 Single-dose vials artesunate (73607-001-01) and 2 vials sterile diluent (NDC 73607-001-02) per carton (NDC 73607-001-11); 4x4 pack containing 4 Single-dose vials artesunate (73607-001-01) and 4 vials sterile diluent (NDC 73607-001-02) per carton (NDC 73607-001-10), Rx only, Mfg for: Amivas, LLC, 1209 Orange St., Wilmington, Delaware 19801.

by AMIVAS (US), LLC

Reason
Lack of Assurance of Sterility: Air filter failed post integrity test leading to a lack of sterility assurance.
Published
October 13, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

ALPHA MALE+ Male Enhancer, fruit chew strips, 1 strip per foil pouch, Distributed by Umbrella Labs, Made in the USA, UPC 8 60003 03770 6. Also manufactured for and distributed by: Alpha Male Plus, Tucson, AZ UPC 8 60003 74518 2 (pouch), UPC 8 60003 74512 0(carton)

by Alpha-Tek LLC

Reason
Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence of tadalafil
Published
October 13, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Phenylbutyrate Powder, 250 Grams, Rx Only, packaged in 500 cc HDPE bottles and 53 mm CRC caps packed in a carton and then in case packs containing 2 bottles. Sigmapharm Laboratories, LLC, Bensalem, PA 19020, NDC 42794-086-14

by SigmaPharm Laboratories LLC

Reason
Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.
Published
October 6, 2021
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.