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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 November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 10,361–10,380 of 21,307 recalls

FDA Recall TerminatedTerminated: August 16, 2022Historical recordClass II

Allergy Relief (fexofenadine hydrochrloride) tablets, 180 mg, 5-count carton, Good Neighbor Pharmacy, Distributed By Amerisource Bergen, 1300 Morris Drive, Chesterbrook, PA 19087, NDC 46122-387-23.

by Aurolife Pharma, LLC

Reason
Failed Impurities/Degradation Specifications
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 16, 2022Historical recordClass II

Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53); b) 30-count cartons (NDC 60000-409-30); c) 45-count bonus cartons (NDC 60000-409-48); d) 45-count cartons (NDC 60000-409-45); CAREone, Distributed by: Foodhold U.S.A., LLC, Landover, MD 20785.

by Aurolife Pharma, LLC

Reason
Failed Impurities/Degradation Specifications
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 16, 2022Historical recordClass II

Fexofenadine Hydrochrloride Tablets USP, 180 mg, 100-count bottle, Distributed by: Aurohealth LLC., 2572 Brunswick Pike, Lawrenceville, NJ 08648, NDC 58602-711-21

by Aurolife Pharma, LLC

Reason
Failed Impurities/Degradation Specifications
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 15, 2022Historical recordClass II

Oxcarbazepine Oral Suspension, USP, 300 mg/5 mL, 250 mL per bottle, Rx Only, Distr. by: West-Ward Pharmaceuticals,Eatontown, NJ. NDC:0054-0199-59

by West-Ward Columbus Inc

Reason
Failed Impurities/Degradation Specificattion
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 3, 2020Historical recordClass II

Anagrelide Capsules, USP, 0.5 mg, 100-count bottle, Rx only, Manufactured in India for: Torrent Pharma Inc., Basking Ridge, NJ 07920, NDC 13668-453-01.

by Torrent Pharma Inc.

Reason
Failed Impurities/Degradation Specifications: High Out Of Specification results for impurities detected during routine stability testing.
Published
September 25, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 12, 2023Historical recordClass II

Soothing Sore Relief (lidocaine) Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-077-14), b) 2 Oz (NDC 69804-077-15), and c) 4 Oz (NDC 69804-077-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

by Ridge Properties, LLC

Reason
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Published
September 25, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 12, 2023Historical recordClass II

Soothing Sore Relief (lidocaine) Cream, 4%, packaged in a) 1 OZ (NDC 69804-074-05), b) 2 OZ (NDC 69804-074-02), and c) 4 OZ (NDC 69804-074-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

by Ridge Properties, LLC

Reason
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Published
September 25, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 12, 2023Historical recordClass II

Superior Pain & Itch Relief (lidocaine) Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-073-14), b) 2 Oz (NDC 69804-073-15), and c) 4 Oz (NDC 69804-073-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

by Ridge Properties, LLC

Reason
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: July 12, 2023Historical recordClass II

Superior Pain & Itch Relief (lidocaine) Cream, 4%, packaged in a) 1 OZ (NDC 69804-070-05), b) 2 OZ (NDC 69804-070-02), and c) 4 OZ (NDC 69804-070-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

by Ridge Properties, LLC

Reason
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: July 12, 2023Historical recordClass II

PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-019-14), b) 2 Oz (NDC 69804-019-15), and c) 4 Oz (NDC 69804-019-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

by Ridge Properties, LLC

Reason
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Published
September 25, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 12, 2023Historical recordClass II

PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream, 4%, packaged in a) 1 OZ (NDC 69804-002-05), b) 2 OZ (NDC 69804-002-02), and c) 4 OZ (NDC 69804-002-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

by Ridge Properties, LLC

Reason
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: December 19, 2019Historical recordClass II

Stavis Seafoods, Inc.

Product
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product o…
Reason
Product may contain elevated levels of histamine.
Published
September 25, 2019
Distribution
Products were distributed in NY,OH,MI,PA…

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FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
7-Select Roasted Red Pepper Hummus with Pretzels 4.1 oz. UPC…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
7-Select Classic Hummus w/ Pretzel 4.1 oz. UPC 52548595272 p…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
7-Select Chipotle Garlic Hummus w/ Pretzels 4.1 oz. UPC 5254…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
Schnuck's Roasted Red Pepper Hummus 8 oz. UPC 41318092363 p…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
Schnuck's Cilantro Jalapeno Hummus 8 oz. UPC 41318092387 pac…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
Schnuck's Traditional Hummus 8 oz. UPC 41318092356 packaged…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
Schnuck's Roasted Garlic Hummus 8 oz. UPC 41318092370 packa…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product
Schnuck's Garden Vegetable Hummus 8 oz. UPC 41318092394 pac…
Reason
Product has potential to be contaminated with Listeria monocytogenes
Published
September 25, 2019
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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