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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.

37,060
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 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 II24,313
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 1,061–1,080 of 19,352 recalls

FDA Recall Ongoing Historical recordClass III

Everolimus tablets 5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977, NDC 49884-125-91

by ENDO USA, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0102-05.

by STAQ Pharma, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date
Published
October 22, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass III

Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0156-02.

by STAQ Pharma, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0104-05.

by STAQ Pharma, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344

by SV Labs Prescott Corporation

Reason
cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Viorele, Desogestrel and Ethinyl Estradiol, USP, 0.15 mg/ 0.02 mg and Ethinyl Estradiol Tablets, USP, 0.01 mg, 3 Blisters each containing 28 Tablets, Rx only, 28 day Regimen, Manufactured by: Glenmark Pharmaceuticals Limited, Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA., Mahwah, NJ, 07430, NDC 68462-318-29.

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Impurities/Degradation Specifications
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b). 500-count(NDC 67877-514-05), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054

by Ascend Laboratories, LLC

Reason
Failed Dissolution Specifications
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 20 mg, Rx Only, a). 90-count(NDC 67877-512-90), b). 500-count (NDC 67877-512-05), c). 1000-count(NDC 67877-512-10),Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

by Ascend Laboratories, LLC

Reason
Failed Dissolution Specifications
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 40 mg, Rx Only, a). 90-count (NDC 67877-513-90), b). 500-count (NDC 67877-513-05), c). 1000-count (NDC 67877-513-10), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

by Ascend Laboratories, LLC

Reason
Failed Dissolution Specifications
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 10 mg, Rx Only a) 90-count bottle (NDC 67877-511-90), b). 500-count bottle (NDC 67877-511-05), c). 1000-count bottle (NDC 67877-511-10) Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

by Ascend Laboratories, LLC

Reason
Failed Dissolution Specifications
Published
October 22, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tavaborole Topical solution 5%, 10 mL bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Changodar, Ahmedabad, India, Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016, NDC 72578-102-04.

by VIONA PHARMACEUTICALS INC

Reason
Discoloration
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1

by IntegraDose Compounding Services LLC

Reason
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

TROPICANA BRANDS GROUP

Product
Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bot…
Reason
A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.
Published
October 22, 2025
Distribution
The adulterated product was distributed…

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FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Medium White Eggs, 18ct Cartons, 15dz pe…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

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FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Large White Eggs, 12ct Cartons, 15dz per…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

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FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Medium White Eggs, Loose Open Skid, 900d…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

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FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

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FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Medium Brown Eggs, Loose Open Skid, 900d…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

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FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Large Brown Eggs, Loose Open Skid, 900dz…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

View recall →

FDA Recall United States Terminated Historical recordClass I

Black Sheep Egg Company, LLC

Product
Free Range Grade AA Medium Brown Eggs, Loose Pack in Boxes,…
Reason
Potential Salmonella contamination.
Published
October 22, 2025
Distribution
Retail and wholesale locations in AR and…

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.