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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 6,401–6,420 of 22,603 recalls

FDA Recall Terminated Historical recordClass II

EPI-PEN 2-PAK (epinephrine injection, USP), Single-Dose Auto-Injectors 0.3 mg, Rx only, Manufactured for: Mylan Specialty LP., NDC 49502-500-02

by Mckesson Medical-Surgical Inc. Corporate Office

Reason
cGMP deviations: Temperature abuse
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Earache Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. NDC 0363-3233-15

by Grato Holdings, Inc.

Reason
Microbial contamination of non-sterile product.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Homeopathic EarAche Ear Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 59779-568-15

by Grato Holdings, Inc.

Reason
Microbial contamination of non-sterile product.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Homeopathic EarAche Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: RITE AID, 30 Hunter Lane, Camp Hill, PA 17011. NDC 11822-3644-3

by Grato Holdings, Inc.

Reason
Microbial contamination of non-sterile product.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-1501-02, Distributed by: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, Vial NDC 0703-1501-01

by Teva Pharmaceuticals USA Inc

Reason
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

B-Complex + Chromic Chloride (Choline Chloride 3%, Inositol 3%, Pyridoxine HCl 2%, Niacinamide 2%, Thiamine HCl 2%, Chlorobutanol 0.5%, Riboflavin 0.05%, Chromic Chloride 0.003%), 30 mL Multi-Dose Vial, packaged in 2 x 30 mL Multi-Dose Vials per carton, US Specialty Formulations, LLC, 116 Research Drive, Bethlehem, PA 18015, P/N: 234-15523

by US Specialty Formulations LLC

Reason
Lack of Assurance of Sterility
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ethanol for Injection 95%, 67 mL Multi-Dose vial, Rx only, US Specialty Formulations, 1403 South Albert Street, Allentown, PA 18103, PN: 69389-06229

by US Specialty Formulations LLC

Reason
Lack of Assurance of Sterility
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE, packaged in a) 5 single-use containers (0.2 mL each vial) (NDC 54092-606-07) and b) 4 pouches x 5 single-use containers (NDC 54092-606-04), Rx Only, Manufactured for: Shire US Inc., 300 Shire Way, Lexington, MA 02421.

by Novartis Pharmaceuticals Corporation

Reason
Failed Impurities/Degradation Specifications.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE, packaged in a) 5 single-use containers (0.2 mL each vial) (NDC 0078-0911-95) and b) 4 pouches x 5 single-use containers (NDC 0078-0911-94), Rx Only, Manufactured by: The Ritedose Corporation Columbia, SC 29203; Distributed by: Novartis Pharmaceuticals Corporation East Hanover, NJ 07936.

by Novartis Pharmaceuticals Corporation

Reason
Failed Impurities/Degradation Specifications.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Xiidra (lifitegrast ophthalmic solution) 5%, packaged in a) 60 Single-Use Containers: 12 pouches x 5 single-use containers (0.2 mL each vial) (NDC 54092-606-01) and b) 5-Single-Use Containers (NDC 54092-606-06), Rx Only, Manufactured for: Shire US Inc., 300 Shire Way, Lexington, MA 02421.

by Novartis Pharmaceuticals Corporation

Reason
Failed Impurities/Degradation Specifications.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Xiidra (lifitegrast ophthalmic solution), packaged in a) 60 Single-Use Containers: 12 pouches x 5 single-use containers (0.2 mL each vial) (NDC 0078-0911-12) and b) 5- Single-Use Containers (NDC 0078-0911-05) Rx Only, Manufactured by: The Ritedose Corporation, Columbia, SC 29203, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936.

by Novartis Pharmaceuticals Corporation

Reason
Failed Impurities/Degradation Specifications.
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

ELITE CONFECTIONERY LTD

Product
ELITE MILK CHOCOLATE HEARTS UPC:73490154485
Reason
Potential contamination with Salmonella
Published
June 15, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Saputo Cheese USA Inc.

Product
Frigo Part-Skim Low Moisture Part Skim Mozzarella Cheese…
Reason
The 2 lb. units of Frigo Low Moisture Part-Skim Mozzarella Cheese are being recalled due to the allergen of milk in the product not being declared on the label.
Published
June 15, 2022
Distribution
A total of 4 retail consignees located i…

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FDA Recall United States Terminated Historical recordClass I

Van Leeuwen Ice Cream

Product
Van Leeuwen Ice Cream -Oat Milk Brown Sugar Chunk - 14 oz.
Reason
Ice cream contains undeclared tree-nuts (cashew and pistachio)
Published
June 15, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

General Mills James Ford Bell Technical Center

Product
dibz Lunch Blox. Entree, Grain, Veggie, Fruit
Reason
Potential Salmonella contamination.
Published
June 15, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

HP Hood LLC

Product
PLANET OAT Chocolate Chip Cookie Dough; OATMILK NON-DAIRY FR…
Reason
Product may contain undeclared peanuts.
Published
June 15, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

The TJX Companies, Inc.

Product
Keats London Vegan Irish Cream Truffles in a 4.93-ounce rou…
Reason
Product(s) may contain undeclared milk.
Published
June 15, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

The TJX Companies, Inc.

Product
Keats London Vegan Hazelnut Dark Chocolate in a 4.93-ounce…
Reason
Product(s) may contain undeclared milk.
Published
June 15, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

The TJX Companies, Inc.

Product
Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.8…
Reason
Product(s) may contain undeclared milk.
Published
June 15, 2022
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Taylor Farms Retail Inc

Product
Trader Joe's Southwestern Chopped Salad Contains: Green Cabb…
Reason
Trader Joes branded Southwestern Chopped Salad Kits was found to contain the incorrect master pack. The master pack includes the allergens of soy and pistachio. Soy was declared on the label, but pistachio was not.
Published
June 15, 2022
Distribution
Product was shipped to two Trader Joe's…

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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.