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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.

37,059
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/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 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 841–860 of 19,636 recalls

FDA Recall United States Completed 2026 recordClass II

House Of Flavors, Inc.

Product
1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6
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 United States Completed 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Ongoing 2026 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 Terminated 2026 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 Terminated 2026 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 Ongoing 2026 recordClass II

Town Food Service Equip Co Inc

Product
Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1Q…
Reason
Product found to contain leachable lead levels.
Published
January 14, 2026
Distribution
AL, AR, AZ, CA, CO, FL, GA, IL, KY, LA,…

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FDA Recall Ongoing 2026 recordClass III

traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only, Manufactured by: Zydus Lifesciences Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-806-10

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Ondansetron Orally Disintegrating Tablets, USP, 4mg, 30 Tablets (3 blistercards each containing 10 tablets), Rx only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, Product of India, NDC 68462-157-13

by Glenmark Pharmaceuticals Inc., USA

Reason
Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4501-14

by Novo Nordisk Inc.

Reason
Presence of Particulate Matter: Hair was found in a prefilled syringe
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4505-14

by Novo Nordisk Inc.

Reason
Presence of Particulate Matter: Hair was found in a prefilled syringe
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL Applicator, CareFusion 213, LLC, El Paso, TX 79912, NDC 54365-401-29

by CareFusion 213, LLC

Reason
Lack of Assurance of Sterlity
Published
January 7, 2026
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.