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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,481–2,500 of 18,349 recalls

FDA Recall Ongoing Historical recordClass III

Clindamycin Phosphate, Topical Solution USP, 1%, 60 mL, Rx Only, Manufactured for and Distributed by: Marlex Pharmaceuticals, Inc., New Castle, DE 19720, NDC 10135-0691-61

by Contract Pharmaceuticals Limited Canada

Reason
Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
Published
March 13, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

LQNN Inc.

Product
BANH PIA Liu Sha Pumpkin Pia Cake, 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 Terminated Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Red Bean 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 Terminated Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Pandan 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 Terminated Historical recordClass I

LQNN Inc.

Product
Vegetarian Pia Cake Mung Bean Pineapple, 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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…

View recall →

FDA Recall United States Terminated Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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

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.