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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 1,041–1,060 of 19,352 recalls

FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61 (Blister pack), NDC 55154-3363-0 (Outer Bag).

by The Harvard Drug Group LLC

Reason
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Published
October 29, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61

by The Harvard Drug Group LLC

Reason
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Published
October 29, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

M.C.I. Foods, Inc.

Product
Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; U…
Reason
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
Published
October 29, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

M.C.I. Foods, Inc.

Product
Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz;…
Reason
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
Published
October 29, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

DEMERS FOOD GROUP LLC

Product
Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Reason
Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne 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
Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. Product…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne 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 Smoked Mozzarella With Hot Links Extra Large, UP…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne 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
Grilled Chicken & Basil Pasta Extra Large UPC 213035 #####.…
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 Basil Bowtie Pasta Salad, UPC 211913 #####. 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…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Spinach Bowtie Pasta Salad, UPC 211426 #####. Pr…
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…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Basil Pesto Bowtie Pasta Salad, UPC 291308 #####…
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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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,…

View recall →

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,…

View recall →

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

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.