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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.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 3,101–3,120 of 21,230 recalls

FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Mungbean Durian, 14oz (400g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
BANH PIA Hopia Cake Mungbean Durian, 9.7oz (275g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Black Sesame Durian, 14oz (400g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
BANH Ba Xa Lady Cake, 260g
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Taro Durian, 14 oz (400g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Mung Bean Pumpkin, 14 oz (400g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: May 14, 2024Historical recordClass I

LQNN Inc.

Product
BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)
Reason
Undeclared allergen; egg
Published
March 13, 2024
Distribution
U.S. distribution to customers in: Alaba…

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FDA Recall United States TerminatedTerminated: March 4, 2025Historical recordClass I

Summer Fresh Salads Inc

Product
Wegmans Harissa Hummus Topped With Harrisa 10.5 ounce (298 g…
Reason
Product contains undeclared sesame.
Published
March 13, 2024
Distribution
Washington D.C., Delaware, Maryland, Mas…

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FDA Recall United States TerminatedTerminated: April 16, 2024Historical recordClass I

T Marzetti Co

Product
Chick-fil-a Polynesian Sauce Cup: 28g single serve food serv…
Reason
Undeclared Allergens - Wheat and Soy
Published
March 13, 2024
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: February 5, 2025Historical recordClass I

Taylor Fresh Foods Inc

Product
COLD CASE, ROASTED STREET CORN SALAD 1/4.78# (KR) Separate K…
Reason
Product has the potential to be contaminated with Listeria monocytogenes.
Published
March 13, 2024
Distribution
U.S. distribution to the following: AL,…

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FDA Recall United States TerminatedTerminated: February 5, 2025Historical recordClass IFDA Announcement

Taylor Fresh Foods Inc

Product
Marketside Bacon Ranch Crunch Chopped Salad Kit 12.76oz UPC…
Reason
Product has the potential to be contaminated with Listeria monocytogenes.
Published
March 13, 2024
Distribution
U.S. distribution to the following: AL,…
Announced by FDA
February 9, 2024

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FDA Recall OngoingHistorical recordClass II

Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42

by Denver Solutions, LLC DBA Leiters Health

Reason
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Moxifloxacin 5mg/ml, 1 ml in a Single- Dose Vial, Rx Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-097-42

by Denver Solutions, LLC DBA Leiters Health

Reason
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42

by Denver Solutions, LLC DBA Leiters Health

Reason
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471

by Seatex LLC

Reason
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033

by Seatex LLC

Reason
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 330 Gal. cases, Distributed by: Magnus, 16005 Gateway Drive, Suite 300, Frisco, TX 75033

by Seatex LLC

Reason
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471

by Seatex LLC

Reason
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published
March 6, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G cases, mountain spring scent, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471.

by Seatex LLC

Reason
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published
March 6, 2024
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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