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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.

37,143
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 15,201–15,220 of 22,149 recalls

FDA Recall United States Terminated Historical recordClass II

Mikawaya

Product
Shirakiku Brand Red Bean Ice Cream 3 gallon foodservice tub
Reason
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
Published
July 5, 2017
Distribution
DC locations in PA, TX, IL, CA, FL.

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FDA Recall United States Terminated Historical recordClass II

Mikawaya

Product
Green Tea Ice Cream: Sold under the brand names of: Trader…
Reason
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
Published
July 5, 2017
Distribution
DC locations in PA, TX, IL, CA, FL.

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FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product
Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz (184g)…
Reason
The firm was notified that the product does not list MILK in the allergen Contains statement, although it is listed in the ingredient statement. They were alerted of this error by a consumer who reported a reaction consistent with a Milk allergy.
Published
July 5, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass II

Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc. Eden Prairie, MN 55344

by Vi-Jon, Inc.

Reason
Presence of foreign substance: glass particle
Published
June 28, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.

by Lucid Pharma LLC

Reason
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Published
June 28, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Star Snacks Co., Llc.

Product
Southern Grove Cashew Halves & Pieces with Sea Salt, Net Wei…
Reason
The firm received notification from a consumer finding a glass fragment in Southern Grove Cashew Halves, 8.oz. Source of glass is unknown. It is suspected the glass fragments came in with the raw material.
Published
June 28, 2017
Distribution
ALDI Distribution Centers. 3/6/2017…

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FDA Recall United States Terminated Historical recordClass I

Blue Diamond Growers

Product
Blue Diamond Almonds Blanc DCD FN C (blanched diced fine);…
Reason
Firm was notified by customer of a positive Salmonella result obtained when testing of the product on receipt.
Published
June 28, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Genetic Edge Compounds LLC

Product
GEC TNT Thermanite 60 Capsules Dietary Supplement in clear p…
Reason
Product contains DMAA and Methylsynephrine.
Published
June 28, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Meijer, Inc #816 - Grand River Packaging

Product
Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., 6/case, packed…
Reason
The firm initiated a voluntary recall of Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., packed in a stand up pouch, due to mislabeling. The label declared cream, milk, and eggs, which were not part of the original formula. The label lacked the following ingredients: Spices, Artificial Flavors, Garlic Powder, Onion Powder, Dextrose, Worcestershire Sauce, Corn Syrup, Salt, Carmel Color, Sugar, Tamarind, Natural Flavor, Malic Acid, Olive Oil, Molasses Sucralose, Bourbon Whiskey, Sulfites & Celery Seeds.
Published
June 28, 2017
Distribution
Domestic: IL, IN, KY, MI, OH, WI,…

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FDA Recall United States Terminated Historical recordClass I

Monfitello

Product
Private Selection Peruvian Inspired Aji Amarillo Culinary Sp…
Reason
The firm was notified that the product may contain peanuts.
Published
June 28, 2017
Distribution
Products were shipped to the following s…

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FDA Recall United States Terminated Historical recordClass I

Monfitello

Product
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINA…
Reason
The firm was notified that the product may contain peanuts.
Published
June 28, 2017
Distribution
Products were shipped to the following s…

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FDA Recall Terminated Historical recordClass III

Montelukast Sodium Oral Granules, 4 mg pouch, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-6040-93

by Mylan Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications; out of specification results for Sulphoxide Impurity and Total Impurities
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

by Complete Pharmacy and Medical Solutions LLC

Reason
Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP, Service Code 2K2227, NDC# 61553-027-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.75g in 300 mL 0.9% Sodium Chloride Injection USP, Service Code 2K2237, NDC# 61553-037-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.5g in 300 mL 0.9% Sodium Chloride Injection USP, Service Code 2K2243, NDC# 61553-043-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 7 mMol 100 mL Bag, Service Code 2K5284, NDC# 61553-0284-48, Total Volume 100.00 mL incorrectly labeled as 102.33 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 20 mMol 100 mL Bag, Service Code 2K5287, NDC# 61553-0287-48, Total Volume 100.00 mL incorrectly labeled as106.67 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 10 mMol 100 mL Bag, Service Code 2K5288, NDC# 61553-0288-48, Total Volume 100.00 mL incorrectly labeled as 103.33 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 15 mMol 100 mL Bag, Service Code 2K5295, NDC# 61553-0295-48, Total Volume 100.00 mL incorrectly labeled as105.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
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.