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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.

37,118
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
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 7,481–7,500 of 18,404 recalls

FDA Recall Terminated Historical recordClass II

Caduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/10 mg*, 30-count bottle, Rx only, Distributed by: Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Germany, NDC 0069-2160-30.

by Pfizer Inc.

Reason
Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture protection.
Published
February 19, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Caduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/20 mg*, 30-count bottle, Rx only, Distributed by: Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Germany, NDC 0069-2180-30.

by Pfizer Inc.

Reason
Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture protection.
Published
February 19, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL dropper bottle, Rx only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701; NDC 50383-901-10.

by Akorn Inc

Reason
Subpotent Drug: Low Out of specification (OOS) assay results for the hydrocortisone portion of this product.
Published
February 19, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Methylphenidate hydrochloride Extended-Release ablets USP (CII), 27 mg, 100-count bottle, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 62037-734-01

by Teva Pharmaceuticals USA

Reason
CGMP deviations: Product bottle may be absent of desiccant.
Published
February 19, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Methylphenidate hydrochloride Extended-Release ablets USP (CII), 18 mg, 100-count bottle, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 62037-725-01

by Teva Pharmaceuticals USA

Reason
CGMP deviations: Product bottle may be absent of desiccant.
Published
February 19, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL), 2 mL Single-dose Vial, Each Tray contains 25 Vials, Intravenous or Intramuscular Use, Rx only, Distributed by Hospira, Inc. Lake Forest, IL 60045, NDC 00409-9094-12 (vial), 00409-9094-22 (tray).

by Pfizer Inc.

Reason
Defective Container: confirmed customer reports for vials with loose metal overseal crimp defects, which may result in lack of assurance of sterility.
Published
February 19, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ethacrynate Sodium for Injection, USP, 50mg/vial, Single Dose Vial, Rx Only, Manufactured by: Cadila Healthcare Limited, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-246-01.

by Zydus Pharmaceuticals USA Inc

Reason
cGMP Deviations
Published
February 19, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Lamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutical Industries Ltd. Haifa Bay, Israel 2624761 Dist. by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532, NDC 51672-4131-1.

by Taro Pharmaceuticals U.S.A., Inc.

Reason
Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.
Published
February 19, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Bulk flour
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Springup Flour Product Code 703220 in 50# bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Sir Lancelot HG Flour Unbl, Enr, Mt / Product Code: 802203…
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Sir Galahad flour / Product Code: 805226 in 50# bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Potentate flour / Prod Code: 802217 in 50# bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Polar Bear Flour UNTR /Prod Code: 710200 in 50# bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
H&R Flour, UNBL, EN, MT / Product Code 706220 in 50# bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
H & R All Purpose Flour BL EN MT /Product Code: 706250 in 50…
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
H & R All Purpose Flour MT/Product Code: 706205 in 50 lbs ba…
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Commander Flr BL ENR BR MT, Product Code 704260 in 50 lbs…
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Commander Flour, Product Code 704220 in 50 lbs bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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FDA Recall United States Terminated Historical recordClass I

Adm Milling

Product
Bova Flour HG, Product Code 804207 in 50 lbs bags
Reason
E.coli O26
Published
February 19, 2020
Distribution
AR CT FL IL IN MA MD MI NJ NY…

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.