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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 1,041–1,060 of 22,574 recalls

FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Pain Away Herbal Supplement, Analgesic & anti-inflammatory p…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Organic Ginger Root Herbal Supplement, Natural anti-inflamma…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Ear Drops Herbal Supplement, Mullein flower alcohol tincture…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Ext…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Baby Soothe Herbal Supplement, Promotes rest, helps ease col…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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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 United States Ongoing Historical recordClass II

Karabetian Import and Distribution, Inc.

Product
Product: Zimi Kunefe Ready to eat (Frozen) Package Size and…
Reason
partially hydrogenated oils (PHOs) in foods exported to the US
Published
December 31, 2025
Distribution
Distributed in the following states: AZ,…

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FDA Recall United States Ongoing Historical recordClass II

Karabetian Import and Distribution, Inc.

Product
Product: Zimi Puff Pastry French Style (frozen) Package Siz…
Reason
partially hydrogenated oils (PHOs) in foods exported to the US
Published
December 31, 2025
Distribution
Distributed in the following states: AZ,…

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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

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FDA Recall Ongoing Historical recordClass II

Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10

by Golden State Medical Supply Inc.

Reason
Presence of Foreign Tablets/Capsules
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

OraVerse, (Phentolamine Mesylate) Injection, 0.4 mg/1.7mL, packaged in a carton containing 10 cartridges, 0.4 mg/1.7mL, Rx only, Made in Canada by Novocol Pharmaceutical of Canada, Inc., Distributed by Septodont, Inc., Louisville, Co, 80027, NDC 0362-0101-10

by Novocol Pharmaceutical of Canada, Inc.

Reason
Defective container: cracked/broken cartridges
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cook-Walte, Carbocaine 3% (30 mg/mL), (mepivacaine hydrochloride Injection, USP), packaged in a carton containing 50 Single-Dose Cartridges, 1.7 mL, Rx only, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 0362-0753-05.

by Novocol Pharmaceutical of Canada, Inc.

Reason
Defective container: cracked/broken cartridges
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Benco dental Graham CHEMICAL CO., Mepivacaine HCI 3% (30 mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, Distributed by Benco Dental 295 Center Point Blvd, Pittston, PA 18640, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 66975-406-51.

by Novocol Pharmaceutical of Canada, Inc.

Reason
Defective container: cracked/broken cartridges
Published
December 24, 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.