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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,061
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
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 1,701–1,720 of 21,591 recalls

FDA Recall Ongoing Historical recordClass II

Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.

by Empower Clinic Services, LLC dba Empower Pharmacy

Reason
Lack of Assurance of Sterility
Published
May 21, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube per Carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France.

by L'Oreal USA

Reason
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
Published
May 21, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatment 0.7 fl. oz. (20 mL: UPC 883140035275) Tube, (benzoyl peroxide 0.5% and benzoyl peroxide 5.5% and salicylic acid 2%), La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France, UPC 883140035282 (kit).

by L'Oreal USA

Reason
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
Published
May 21, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-Posay, France, UPC 883140500759.

by L'Oreal USA

Reason
Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.
Published
May 21, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

East CK Trading Inc.

Product
PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK…
Reason
Product contains undeclared sulfites (7.49mg/serving)
Published
May 21, 2025
Distribution
Multiple states

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FDA Recall United States Completed Historical recordClass II

Advance Food International Inc.

Product
National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.:…
Reason
Product contains elevated levels of lead (0.0649 mg/kg)
Published
May 21, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Black Cherry Yogurt Parfait, 8oz, Plastic cups with pl…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Strawberry-Banana Yogurt Parfait, 8oz, Plastic cups w…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Passion Fruit Yogurt Parfait, 8oz, Plastic cups with p…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Coconut Yogurt Parfait, 8oz, Plastic cups with plastic…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plast…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Raspberry Yogurt Parfait, 8oz, Plastic cups with plast…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Lemon Yogurt Parfait, 8oz, Plastic cups with plastic i…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic i…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Mango Yogurt Parfait, 8oz, Plastic cups with plastic i…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Blueberry Yogurt Parfait, 8oz, Plastic cups with plast…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Vanilla Yogurt Parfait, 8oz, Plastic cups with plastic…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Ongoing Historical recordClass I

Knockroe Inc

Product
Bonya Strawberry Yogurt Parfait, 8oz, Plastic cups with plas…
Reason
Undeclared Almonds
Published
May 21, 2025
Distribution
The recalled product was distributed to…

View recall →

FDA Recall Ongoing Historical recordClass II

TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0121-01

by BSO LLC

Reason
Presence of Particulate Matter: Glass particles were found in pellet vials.
Published
May 14, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0122-01

by BSO LLC

Reason
Presence of Particulate Matter: Glass particles were found in pellet vials.
Published
May 14, 2025
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.