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Recall totals

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

37,448
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snack-right-super-foods-inc-dba-brads-raw-chips-recalls-brads-crunchy-kale-veggie-chips-duePublished November 2, 2026
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 7,041–7,060 of 18,373 recalls

FDA Recall United States TerminatedTerminated: February 18, 2021Historical recordClass I

Red Monkey Foods Inc

Product
Herbes de Provence packaged in the following ways: 1) Wor…
Reason
An ingredient (parsley) which was repacked into consumer packages and used to manufacture other herb blends tested positive for Salmonella and was recalled by the supplier.
Published
October 28, 2020
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 18, 2021Historical recordClass I

Red Monkey Foods Inc

Product
Dried Parsley packaged in the following ways: 1) World Ma…
Reason
An ingredient (parsley) which was repacked into consumer packages and used to manufacture other herb blends tested positive for Salmonella and was recalled by the supplier.
Published
October 28, 2020
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: November 16, 2020Historical recordClass II

Desert Premium Group, LLC

Product
Trader Joe's Hatch Valley Salsa, 12 oz. jars packed into tra…
Reason
One batch of salsa had a recorded equilibrium pH of 6.65.
Published
October 28, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 3, 2020Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku brand Black Fungus (Kikurage); 5 lb. bag, 6 x 5 l…
Reason
California Department of Public Health sampled and tested Shirakiku brand Black Fungus and found it contain Salmonella ssp. serogroup B.
Published
October 28, 2020
Distribution
AR, CA, CO, CT, DE, DC, FL, GA, HI. IA,…

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FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Chocolate Celebration Cake, 1…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Fall Frost Pumpkin Cupcake, 8…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Chewy Chocolatey Brownie Bite…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Frosty Zucchini Cupcakes, 8.0…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Chocolate Cupcakes with Vanil…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Very Vanilla Cupcakes with Va…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 2, 2021Historical recordClass II

Lucky Spoon Bakery, LLC

Product
Lucky Spoon Bakery Gluten Free Utterly Almond Muffins, 7.25…
Reason
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Published
October 21, 2020
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: January 28, 2021Historical recordClass I

Seneca Foods Corporation

Product
Cinnamon Apple Crisps packaged under the following Brands an…
Reason
Product may be contaminated with Salmonella.
Published
October 21, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass III

NYSTATIN ORAL SUSPENSION, USP 100,000 units per mL Contains: Alcohol 0.5% v/v (Bubblegum Flavored) 16 fl. oz. (480 mL) Manufactured by: VistaPharm, Inc. Largo FL 33771, USA NDC 66689-008-16 UPC 6668900816,

by VistaPharm, Inc.

Reason
Failed Impurties/Degradation Specifications: out of specification results for an impurity for one lot
Published
October 14, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 22, 2022Historical recordClass III

Citalopram Oral Solution, USP 20 mg/10 mL, 10 mL unit dose cups, Rx Only, Mfg for: Pharmaceutical Associates, Inc. Greenville, SC 29605 NDC 0121-1696-40

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason
Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
Published
October 14, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 1, 2022Historical recordClass II

Eye Itch Relief, Ketotifen Fumarate Ophthalmic Solution 0.035%, Sterile, 5 mL, Distributed by CVS Pharmacy, Inc. Woonsocket, RI 02895, NDC 59779-920-01

by Akorn, Inc.

Reason
CGMP Deviations
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 25, 2022Historical recordClass II

pH-D Feminine Health Boric Acid Vaginal Suppositories, 24 vaginal suppositories per box, 600 mg each, pH-D Feminine Health, LLC Madison, TN 37115, UPC Code: 3 49597 00044 5.

by pH-D Feminine Health

Reason
Marketed without an Approved NDA/ANDA.
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 22, 2022Historical recordClass III

Nymalize (nimodipine) oral solution, 60 mg/20 mL, 12 Unit-Dose Cups and 12 Oral Syringes, 2 inner cartons per outer shipping carton, Rx Only, Distributed by arbor Atlanta, GA, NDC 24338-200-12

by Arbor Pharmaceuticals Inc.

Reason
Subpotent Drug
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 26, 2024Historical recordClass I

blumen ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT, (ethyl alcohol 70% v/v) Packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4, b) 7.5 fl oz / 221 ml bottle, UPC 8 14266 02362 4, Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, San Antonio, Texas, 78257, Made in Mexico.

by 4e Brands North America, Llc

Reason
Chemical Contamination and Subpotent Drug: Product tested to contain methanol as well as below the labeled claim for ethanol content.
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 26, 2024Historical recordClass I

blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% natural boost with tea tree oil (70% ethyl alcohol), 33.8 fl oz / 1 L bottle, Distributed in USA and Canada by: 4e Brands 4e Brands Northamerica LLC. 17806 IH-10W, Suite 300, San Antonio, Texas, 78257. Made in Mexico. UPC 8 14266 02374 7

by 4e Brands North America, Llc

Reason
Chemical Contamination and Subpotent Drug: Product tested to contain methanol as well as below the labeled claim for ethanol content.
Published
October 7, 2020
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 26, 2024Historical recordClass I

blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v), Packaged as a) 2 fl oz / 60 ml bottle, UPC 8 14266 02371 6 b) 17 fl oz / 503 ml bottle with blue cap or pump bottle, UPC 8 14266 02409 6 c) 33.8 fl oz / 1 L straight or curved bottle, UPC 8 14266 02369 3. Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, San Antonio, Texas, 78257, Made in Mexico.

by 4e Brands North America, Llc

Reason
Chemical Contamination and Subpotent Drug: Product tested to contain methanol as well as below the labeled claim for ethanol content.
Published
October 7, 2020
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.

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