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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 981–1,000 of 18,349 recalls

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Basil Pesto Bowtie Pasta Salad, UPC 216492 #####. Product wa…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Basil Pesto Bowtie Pasta Salad, UPC 294921 #####. Product wa…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Prod…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass II

Southwind Foods LLC dba Great American Seafood Imports Co.

Product
Great American branded Frozen raw shrimp skewer; 1lb bag U…
Reason
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
Published
October 29, 2025
Distribution
Distribution includes 26 domestic retail…

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FDA Recall United States Terminated Historical recordClass II

Southwind Foods LLC dba Great American Seafood Imports Co.

Product
Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag…
Reason
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
Published
October 29, 2025
Distribution
Distribution includes 26 domestic retail…

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FDA Recall United States Terminated Historical recordClass II

Southwind Foods LLC dba Great American Seafood Imports Co.

Product
Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag…
Reason
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
Published
October 29, 2025
Distribution
Distribution includes 26 domestic retail…

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FDA Recall United States Terminated Historical recordClass II

Southwind Foods LLC dba Great American Seafood Imports Co.

Product
Arctic Shores; Best Yet; Great American; Master Catch brande…
Reason
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
Published
October 29, 2025
Distribution
Distribution includes 26 domestic retail…

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FDA Recall United States Terminated Historical recordClass II

Southwind Foods LLC dba Great American Seafood Imports Co.

Product
Arctic Shores; Best Yet; Great American; Master Catch brande…
Reason
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
Published
October 29, 2025
Distribution
Distribution includes 26 domestic retail…

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FDA Recall United States Terminated Historical recordClass II

SNO PAC FOODS INC

Product
Frozen Organic Spinach Net Wt. 10 oz (283.5g) poly bags pack…
Reason
Organic Spinach has the potential to be contaminated with Listeria monocytogenes.
Published
October 29, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product
Smoked Mozzarella Penne Salad, packaged in plastic container…
Reason
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
Published
October 29, 2025
Distribution
AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product
Basil Pesto Bowtie Pasta Salad, packaged in plastic containe…
Reason
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
Published
October 29, 2025
Distribution
AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

Sprouts Farmers Market

Product
Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refr…
Reason
Product may contain Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AL, AZ, CA, CO, DE, FL, G…

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FDA Recall Ongoing Historical recordClass II

Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ, 08816, Manufactured by Suven Pharmaceuticals Limited, Pashamylaram, Telangana, 205307, India. NDC# 16571-691-01

by Rising Pharma Holding, Inc.

Reason
Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength Carbidopa, Levodopa, and Entacapone film-coated tablets (25 mg/100 mg/200 mg).
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Fasenra (benralizumab) Injection, 30 mg/mL, one single-dose pre-filled syringe, Rx only, Manufactured by: AstraZeneca AB, Sweden, Distributed by: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850. NDC 0310-1730-30

by ASTRAZENECA PHARMACEUTICALS

Reason
Lack of Assurance of Sterility:
Published
October 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose]

by Amerisource Health Services LLC

Reason
CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Published
October 22, 2025
Distribution
Nationwide

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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

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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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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.