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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 October 2026.

37,340
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 1,861–1,880 of 25,393 recalls

FDA Recall United States TerminatedTerminated: September 17, 2025Historical recordClass I

SHEEHAN BROTHERS VENDING

Product
Sheehan Brothers Vending Pepperoni Pizza Mini Sub, 4.8 oz (1…
Reason
Undeclared sesame
Published
August 6, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: September 17, 2025Historical recordClass I

SHEEHAN BROTHERS VENDING

Product
Sheehan Brothers Vending Italian Mini Sub, 6.1 oz (174g), in…
Reason
Undeclared sesame
Published
August 6, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: September 17, 2025Historical recordClass I

SHEEHAN BROTHERS VENDING

Product
Sheehan Brothers Vending Spicy Chicken Sandwich, 6.5 oz (184…
Reason
Undeclared sesame
Published
August 6, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: September 17, 2025Historical recordClass I

SHEEHAN BROTHERS VENDING

Product
Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), indivi…
Reason
Undeclared sesame
Published
August 6, 2025
Distribution
Multiple states

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FDA Recall OngoingHistorical recordClass II

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton)

by Cipla USA, Inc.

Reason
Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
Published
July 30, 2025
Distribution
Nationwide

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FDA Recall TerminatedTerminated: January 5, 2026Historical recordClass II

clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, Naples, Florida 34108, NDC# 68180-492-01

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry.
Published
July 30, 2025
Distribution
Nationwide

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FDA Recall CompletedHistorical recordClass III

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.

by Imprimis NJOF, LLC

Reason
Sub-Potent Drug: Subpotent assay results during stability testing.
Published
July 30, 2025
Distribution
Nationwide

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FDA Recall CompletedHistorical recordClass II

Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01

by Imprimis NJOF, LLC

Reason
Sub-Potent Drug: Subpotent assay results during stability testing.
Published
July 30, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: June 18, 2026Historical recordClass II

MING HONG INTERNATIONAL INC.

Product
Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradis…
Reason
Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5.
Published
July 30, 2025
Distribution
Product was distributed to wholesale dis…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 co…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product
Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20-…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 c…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 co…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: August 18, 2025Historical recordClass II

LEWIS BAKERIES

Product
Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/…
Reason
Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.
Published
July 30, 2025
Distribution
Product was distributed to: TN, KS, AR,…

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FDA Recall United States TerminatedTerminated: September 12, 2025Historical recordClass II

Turkeyfoot Creek Creamery LLC

Product
Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream…
Reason
Undeclared allergen - soy
Published
July 30, 2025
Distribution
Products were distributed to six (6) ret…

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FDA Recall United States TerminatedTerminated: September 12, 2025Historical recordClass II

Turkeyfoot Creek Creamery LLC

Product
Turkeyfoot Creek Creamery Mocha Artisan Ice Cream, One Pint…
Reason
Undeclared allergen - soy
Published
July 30, 2025
Distribution
Products were distributed to six (6) ret…

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FDA Recall United States TerminatedTerminated: September 12, 2025Historical recordClass II

Turkeyfoot Creek Creamery LLC

Product
Turkeyfoot Creek Creamery Cacao Artisan Ice Cream, One Pint…
Reason
Undeclared allergen - soy
Published
July 30, 2025
Distribution
Products were distributed to six (6) ret…

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FDA Recall United States TerminatedTerminated: September 12, 2025Historical recordClass II

Turkeyfoot Creek Creamery LLC

Product
Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, On…
Reason
Undeclared allergens - soy and wheat
Published
July 30, 2025
Distribution
Products were distributed to six (6) ret…

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FDA Recall United States TerminatedTerminated: September 12, 2025Historical recordClass II

Turkeyfoot Creek Creamery LLC

Product
Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Crea…
Reason
Undeclared allergens - soy and wheat
Published
July 30, 2025
Distribution
Products were distributed to six (6) ret…

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FDA Recall United States TerminatedTerminated: September 12, 2025Historical recordClass II

Turkeyfoot Creek Creamery LLC

Product
Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cr…
Reason
Undeclared allergens - soy and wheat
Published
July 30, 2025
Distribution
Products were distributed to six (6) ret…

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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