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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 October 2026.

37,268
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 1,021–1,040 of 21,683 recalls

FDA Recall United States Completed2026 recordClass II

House Of Flavors, Inc.

Product
2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
Reason
Undeclared soy lecithin
Published
January 21, 2026
Distribution
AL AZ CT GA IA IL IN KY MI MN MO NC NJ N…

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FDA Recall Ongoing2026 recordClass II

Rosuvastatin Tablets, USP, 10 mg, Rx Only, 50 Tablets (5 x 10) Unit Dose per carton, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 50268-709-15

by AvKARE

Reason
Out of specification for dissolution.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass I

ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887

by Medinatura New Mexico, inc.

Reason
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass I

ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863

by Medinatura New Mexico, inc.

Reason
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0522-01. Case label: SpecGx LLC, NDC 0406052201, Exp. 2027/03, Lot: 0522J23493

by SpecGx, LLC

Reason
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01.

by SpecGx, LLC

Reason
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06.

by Imprimis NJOF, LLC

Reason
Presence of particulate matter - Glass like particles.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01.

by Imprimis NJOF, LLC

Reason
Presence of particulate matter - Glass like particles.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-512-0.1

by Imprimis NJOF, LLC

Reason
Presence of particulate matter - Glass like particles.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass III

Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-176-30

by Alembic Pharmaceuticals Limited

Reason
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 5, 20262026 recordClass I

South Asian Food Inc.

Product
Bengal King Jhal Chanachur food treats 12.34oz (350gm)
Reason
Contains undeclared peanuts
Published
January 14, 2026
Distribution
Multiple states

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FDA Recall United States Ongoing2026 recordClass II

MAYEJ COMERCIALIZADORA S. de R.L. de C.V.

Product
Italian Parsley packaged in 24lb boxes, 40 bunches per box i…
Reason
pathogen Cyclospora cayetanensis
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 11, 20262026 recordClass II

ZIYAD BROTHERS IMPORTING

Product
Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 re…
Reason
May contain partially hydrogenated oils
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 11, 20262026 recordClass II

ZIYAD BROTHERS IMPORTING

Product
Baraka French Style Puff Pastry 1lb and 1.5lbs sizes, UPCs 8…
Reason
May contain partially hydrogenated oils
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall United States Completed2026 recordClass I

Ambriola Co., Inc., The

Product
Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup…
Reason
Product tested positive for Listeria Monocytogenes.
Published
January 14, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Completed2026 recordClass I

Ambriola Co., Inc., The

Product
Ambriola Piccante grated Pecorino Romano, 5 and 10-pound pla…
Reason
Product tested positive for Listeria Monocytogenes.
Published
January 14, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Completed2026 recordClass I

Ambriola Co., Inc., The

Product
Boar's Head Pecorino Romano Grated, 5-pound plastic bag (uni…
Reason
Product tested positive for Listeria Monocytogenes.
Published
January 14, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Completed2026 recordClass I

Ambriola Co., Inc., The

Product
Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units…
Reason
Product tested positive for Listeria Monocytogenes.
Published
January 14, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Completed2026 recordClass I

Ambriola Co., Inc., The

Product
Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid,…
Reason
Product tested positive for Listeria Monocytogenes.
Published
January 14, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Completed2026 recordClass I

Ambriola Co., Inc., The

Product
Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (un…
Reason
Product tested positive for Listeria Monocytogenes.
Published
January 14, 2026
Distribution
The recalled product was distributed to…

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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.