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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.

36,950
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 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)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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 II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 701–720 of 17,260 recalls

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

View recall →

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

View recall →

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 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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FDA Recall United States Ongoing 2026 recordClass II

Tom Bumble LLC

Product
Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Cho…
Reason
Foreign material.
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg, 8 packets per carton, Rx Only, Manufactured for: Merck Sharp & Doohme LLC, Rahway, NJ 07056 USA, Manufactured by: N.V. Organon, 5349 AB Oss, The Netherlands, a subsidiary of Organon & Co., Jersey City, NJ 07302, USA NDC 0085-2224-02.

by Merck Sharp & Dohme LLC

Reason
Presence of particulate matter: potential presence of metal particulates in the product.
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ 07065, USA, Manufactured by: Novo Nordisk Production Ireland Limited Athlone, Ireland, NDC 0006-3066-03

by Merck Sharp & Dohme LLC

Reason
Presence of particulate matter: potential presence of metal particulates in the product.
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Silvestri Sweets Inc dba Carousel Candies

Product
Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz.…
Reason
Undeclared pecan
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Silvestri Sweets Inc dba Carousel Candies

Product
Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pou…
Reason
Undeclared wheat
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08

by SUN PHARMA /TARO

Reason
Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose Vials per carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, 10mL Multiple-dose vial, NDC 70069-161-01; 10x10mL Multiple-dose vials per Carton, NDC 70069-161-01.

by SOMERSET THERAPEUTICS LLC

Reason
Subpotent product:out of specification assay results observed during long term stability testing.
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cisatracurium Besylate Injection USP, 200mg/20mL*(10mg/mL), 10 x 20 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single dose 20mL vial NDC 70069-151-01; 10 x 20 Single dose vials per Carton, NDC 70069-151-10.

by SOMERSET THERAPEUTICS LLC

Reason
Subpotent product:out of specification assay results observed during long term stability testing.
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cisatracurium Besylate Injection USP, 10 mg/5 mL* (2mg/mL), 10 x 5 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single-dose 5 mL vial NDC 70069-141-01; 10x5 mL single dose vial per Carton NDC 70069-141-10.

by SOMERSET THERAPEUTICS LLC

Reason
Subpotent product:out of specification assay results observed during long term stability testing.
Published
December 24, 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.