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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 6,581–6,600 of 18,020 recalls

FDA Recall Terminated Historical recordClass II

DCL SA Scalp Therapy Shampoo (Salicylic Acid 3%) 300 ml/10.1 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 357486503120

by Milbar Laboratories, Inc.

Reason
GMP Deviations
Published
November 25, 2020
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Terminated Historical recordClass II

DCL AHA Lightening Gel (hydroquinone 2%), 30 ml/1 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 357486500471

by Milbar Laboratories, Inc.

Reason
GMP Deviations
Published
November 25, 2020
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Terminated Historical recordClass II

DCL B Prox10 Anti-Blemish Wash (Benzoyl Peroxide 10%), 200 ml/6.7 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 0357486500853

by Milbar Laboratories, Inc.

Reason
GMP Deviations
Published
November 25, 2020
Distribution
Product was distributed throughout the U…

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FDA Recall Terminated Historical recordClass II

DCL Active Mattifying Cleanser (Salicylic Acid 2%), 125mL/4.2 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 357486509627

by Milbar Laboratories, Inc.

Reason
GMP Deviations
Published
November 25, 2020
Distribution
Product was distributed throughout the U…

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FDA Recall Ongoing Historical recordClass II

NEXT ADVANCED ANTIBACTERIAL HAND SANITIZER (Ethyl Alcohol 70%), 8 FL OZ (236 ML) bottle, Made in Mexico, Distributed by: Genomma Lab USA Inc., Houston, TX 77027. UPC 6 50240 05357 3

by Albek De Mexico S.A. De C.V.

Reason
CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Published
November 25, 2020
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Assured Instant Hand Sanitizer Vitamin E and Aloe (Ethyl Alcohol 70% v/v), 8 fl oz/ 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico, UPC 639277928597

by Albek De Mexico S.A. De C.V.

Reason
CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Published
November 25, 2020
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Assured Instant Hand Sanitizer Aloe & Moisturizers (Ethyl Alcohol 70% v/v) 8 fl oz / 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico.UPC 639277928610

by Albek De Mexico S.A. De C.V.

Reason
CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Published
November 25, 2020
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Modesa INSTANT HAND SANITIZER with Moisturizers and Aloe Vera (ethyl alcohol 70% v/v) 8 fl oz (237 mL) bottle, Distributed by: Midwood brands, LLC 10611 Monroe RD. Mathews, NC 28105 Made in Mexico UPC 3 2251 38042 6

by Albek De Mexico S.A. De C.V.

Reason
CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Published
November 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

NuuxSan Instant ANTIBACTERIAL HAND SANITIZER, 70% Ethyl Alcohol (ethyl alcohol 70%), 8 fl oz. 237 mL bottle, Distributed by PCM North America LLC 9543 Bassonnet ST. STE 307, Houston, TX 77036, Made in Mexico, UPC 7 13620 00017 5

by Albek De Mexico S.A. De C.V.

Reason
CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Published
November 25, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Union (black) salve packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; d) 8 oz.; e) 16 oz.; and f) 32 oz. jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663

by H & H Remedies, LLC

Reason
CGMP Deviations
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx only, Manufactured for: Baxter Healthcare Corporation Deerfield, IL 60015 USA, Manufactured by: Baxter Pharmaceuticals India Private Ltd Ahmedabad 382213 India, NDC 36000-092-10

by Baxter Healthcare Corporation

Reason
Presence of particulate matter in solution - black and transparent particles
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Vapor Ointment packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; and d) 8 oz jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663

by H & H Remedies, LLC

Reason
CGMP Deviations
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663

by H & H Remedies, LLC

Reason
CGMP Deviations
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Mesalamine Delayed-Release Tablets, USP 1.2 gram (Once-Daily), 120 Tablets bottle, Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 NDC 42291-564-12

by AVKARE Inc.

Reason
Failed Dissolution Specifications
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Mesalamine Delayed-Release Tablets, USP 1.2 gram, 120 tablets per bottle, Rx Only, Manufactured by: Actavis Laboratories, FL, Inc., Fort Lauderdale, FL 33314, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054, NDC 0591-2245-22.

by Teva Pharmaceuticals USA

Reason
Failed Dissolution Specifications: Out-of-specification dissolution results were obtained during stability testing.
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Starwest Botanicals, Inc

Product
Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia…
Reason
Direct customer tested product upon receipt and had a positive result for Salmonella.
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Starwest Botanicals, Inc

Product
Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia…
Reason
Direct customer tested product upon receipt and had a positive result for Salmonella.
Published
November 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534, NDC 68382-772-77

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Dissolution Specification
Published
November 11, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534, NDC 68382-771-77

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Dissolution Specification
Published
November 11, 2020
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-055-01

by Nostrum Laboratories Inc

Reason
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
Published
November 11, 2020
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.