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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 November 2026.

37,449
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Most affected stateHawaii 200 recalls mention this state

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Download matching recalls as CSV

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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 9,661–9,680 of 21,307 recalls

FDA Recall TerminatedTerminated: October 19, 2020Historical recordClass III

Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by: Lupin Limited, Pithampur (M.P.), INDIA, NDC: 68180-429-03.

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: Out-of-specification result observed in any other individual impurity.
Published
January 8, 2020
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 8, 2023Historical recordClass I

Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil package, 725mg per capsule, Distributed by Silver Bullet Ltd, Golden Springs, CO, USA, UPC: 610877392698.

by Natures Rx

Reason
Marketed Without an Approved NDA/ANDA; Product contains undeclared active ingredient - Sildenafil.
Published
January 8, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 3, 2022Historical recordClass II

Ranitidine Syrup (Ranitidine Oral Solution USP), 15 mg/mL, 150 mg/10 mL per cup, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio. (a) Case of 50 cups (NDC 60687-260-69) (b) Case of 40 cups (NDC 60687-260-23 (c) Unit Dose Cup (NDC 60687-260-69)

by American Health Packaging

Reason
CGMP Deviations: Presence of NDMA impurity detected in product.
Published
January 8, 2020
Distribution
Nationwide

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

SARA LEE FROZEN FOODS

Product
Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pa…
Reason
undeclared FD & C Red 40
Published
January 8, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: February 20, 2020Historical recordClass III

Frito-Lay, Inc.

Product
Classic Lays potato chips 2 3/4 oz. UPC 28400 42054; Classic…
Reason
Water from a roof leak may have dripped on chips prior to packaging
Published
January 8, 2020
Distribution
Connecticut, Delaware, New Hampshire, Ne…

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FDA Recall TerminatedTerminated: August 17, 2023Historical recordClass II

Estriol [(16a, 17B)-Estra-1,3,5(10)-triene-3,16,17-triol; Oestriol] Micronized, USP, CAS 50-27-1, packaged in a) 1 G glass bottles, b) 5 G glass bottles, c) 25 G glass bottles, d) 100 G glass bottles, e) 500 G glass bottles, and f) 1 KG plastic bottles, Rx Only, Spectrum Chemical Mfg Corp., Gardena, CA 90248.

by Spectrum Laboratory Products

Reason
Subpotent Drug: Supplier indicated assay results did not meet specifications.
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 9, 2021Historical recordClass III

NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 254.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

by PharMEDium Services, LLC

Reason
Subpotent Drug
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 9, 2021Historical recordClass III

NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

by PharMEDium Services, LLC

Reason
Subpotent Drug
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 9, 2021Historical recordClass III

NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

by PharMEDium Services, LLC

Reason
Subpotent Drug
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 1, 2020Historical recordClass II

Ferris Coffee and Nut Company, Inc.

Product
R.H. Macys & Co. Cinnamon Roasted Almonds, in 10oz metal tin…
Reason
Incorrect product label on back panel
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: May 1, 2020Historical recordClass II

Ferris Coffee and Nut Company, Inc.

Product
R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts wi…
Reason
Incorrect product label on back panel, undeclared cashew, pecan, milk and soy
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Trader Joes Queso Fundido 16oz, SKU 646574
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Trader Joe's Tofu Spring Rolls 7oz, SKU 921510
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Trader Joe's Shrimp Spring Rolls 7oz, SKU 908795
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Trader Joe's 10oz Banh Mi Style Salad w/ Tofu, SKU 614719
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Trader Joe's 8.4oz Smoked Salmon Poke Bowl, SKU 603751
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Okami brand 8pc Salmon Philly Roll, SKU 28113
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Okami OK Tempura Shrimp Roll, 6pc w/ Sweet and Dynamite Sauc…
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Okami 8pc SEAFOOD COMBO 6 SURIMI 2 EBI SHRIMP, SKU 28262
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: March 30, 2020Historical recordClass I

Fuji Food Products, Inc.

Product
Okami brand 16pcs Sushi Platter, SKU 28201
Reason
RTE products potentially contaminated with Listeria monocytogenes.
Published
January 1, 2020
Distribution
Multiple states

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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