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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 8,641–8,660 of 22,138 recalls

FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER FRUIT PALOOZA, 22oz Clear plastic containe…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

View recall →

FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER MIXED FRUIT CUP 6 OZ, 6oz Clear plastic co…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER FRUIT FRENZY BOWL LARGE BOWL, 40oz Clear p…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER FRUIT TRAY, 49oz Clear plastic container,…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER FRUIT TRAY WITH DIP, 49oz Clear plastic co…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER MIXED MELON SLICES, 24oz Clear plastic con…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER MELONS & BERRIES WITH DIP, 22oz Clear plas…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER TRIPLE TREAT & MELON, 22oz Clear plastic c…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER CANTALOUPE AND HONEYDEW SLICES, 24oz Clear…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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FDA Recall United States Terminated Historical recordClass I

Meijer Inc./Traffic Dept.

Product
FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear p…
Reason
potential risk of Salmonella
Published
November 18, 2020
Distribution
Meijer stores in Michigan, Ohio, Indiana…

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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

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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

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FDA Recall Ongoing Historical recordClass II

Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-056-01

by Nostrum Laboratories Inc

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

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FDA Recall Terminated Historical recordClass III

Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee, India, Marketed by: Jubilant Cardista Pharmaceuticals, Inc., Salisbury, MD NDC 59746-0306-32

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Subpotent
Published
November 11, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Fluocinonide Ointment USP 0.05%, packaged in: a) 15 gm tube, NDC 52565-0040-15, b) 30 gm tube, NDC 52565-0040-30 c) 60 gram tube, NDC 52565-0040-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310

by Teligent Pharma, Inc.

Reason
Failed Impurities/Degradation - Out-of-specification results for Fluocinolone Acetonide impurity.
Published
November 11, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Time-Cap Labs, Inc. Metformin Hydrochloride Extended Release Tablets USP 750 mg, 100 count bottles, Rx Only Manufactured for: Time-Cap Labs, Inc. 7 Michael Avenue Farmingdale, NY 11735, USA Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83, Verna Indl. Estate. Verna Goa-403 722 India NDC 49483-624-01

by Marksans Pharma Limited

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

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FDA Recall Terminated Historical recordClass II

Time-Cap Labs, Inc. Metformin Hydrochloride Extended-Release Tablets USP 500 mg, a) 90 count (NDC 49483-623-09) b) 100 count (49483-623-01) c) 500 count (NDC 49483-623-50) and d) 1000 count (NDC 49483-623-10) bottles, Rx Only Manufactured for: Time-Cap Labs, Inc. 7 Michael Avenue Farmingdale, NY 11735, USA, Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83, Verna Indl. Estate. Verna Goa-403 722 India NDC 49483-623-50

by Marksans Pharma Limited

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

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FDA Recall Terminated Historical recordClass II

metformin HCL ER 750 mg Rx only Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 tablets NDC: 43063-902-30; b) 60 tablets NDC: 43063-902-60

by PD-Rx Pharmaceuticals, Inc.

Reason
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
Published
November 11, 2020
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass II

metformin HCL ER 500 mg, a) 30 tablets NDC: 72789-009-30; b) 60 tablets NDC: 72789-009-60; c) 90 tablets NDC: 72789-009-90; d) 180 tablets NDC: 72789-009-93 bottles, Rx only, Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127

by PD-Rx Pharmaceuticals, Inc.

Reason
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
Published
November 11, 2020
Distribution
Multiple states

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.