Data Explorer

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.

37,139

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

State: MT ×
Clear all

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.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated September 24, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

Download CSV

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Bone Builder, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0012-1 and Tester NDC 61096-1012-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

MenoPower, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0014-1 and Tester NDC 61096-1014

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Woman Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879 NDC 61096-0034-1 and Tester NDC 61096-1034-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Brain Power,Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0033-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Man Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0025-1 and Tester NDC 61096-1025-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Rejuvenation Plus, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879 NDC 61096-0035-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Bakkavor Foods USA, Inc.

Product: Trader Joe's Tomato & Basil Hummus Dip, 7 oz. plastic contai…
Reason: Hummus was recalled due to potential Salmonella and/or Listeria monocytogenes contamination
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Bakkavor Foods USA, Inc.

Product: Trader Joe's Hummus quartet; 20 oz. plastic container; Spic…
Reason: Hummus was recalled due to potential Salmonella and/or Listeria monocytogenes contamination
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

World Variety Produce Inc.

Product: Melissa's Hatch Chile Clean Snax, with Chia and flaxseed; 6.…
Reason: Firm discovered that Hatch Chile Clean Snax lists peanuts in the ingredient list but does not list peanuts under the allergen information.
Published: November 7, 2018
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

AJINOMOTO WINDSOR INC

Product: Allsup's Hatch Green Chile & Cheese Burrito, 72/4.5 oz burri…
Reason: Firm was notified by a supplier of a voluntary recall of diced green peppers due to the potential contamination of Salmonella and/or Listeria.
Published: November 7, 2018
Distribution: Product distributed in Arizona, Californ…

View recall →

FDA Recall United States Terminated Historical recordClass II

AJINOMOTO WINDSOR INC

Product: Posada Hatch Green Chile & Cheese Burrito, 72/4.5 oz burrito…
Reason: Firm was notified by a supplier of a voluntary recall of diced green peppers due to the potential contamination of Salmonella and/or Listeria.
Published: November 7, 2018
Distribution: Product distributed in Arizona, Californ…

View recall →

FDA Recall Terminated Historical recordClass II

Bumetanide Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove, MN 55369, NDC 0832-0542-11

by Upsher Smith Laboratories, Inc.

Reason: Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Bumetanide Tablets, USP, 1 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove, MN 55369, NDC 0832-0541-11

by Upsher Smith Laboratories, Inc.

Reason: Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Prednisolone and Gatifloxacin Ophthalmic Solution, 1%/0.5%, 3 mL dropper bottle, Rx Only, 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy LLC

Reason: Presence of precipitate
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lidocaine 1% + Epinephrine 1:100,000 (MDV) INJ SOL, 50 mL per glass vial, Rx only, 340 West State Street, Unit 9, Athens, OH 45701. NDC 7073197450

by RXQ Compounding LLC

Reason: Subpotent drug: During testing of the retention sample, the firm discovered that the product was sub-potent.
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Metoprolol Succinate Extended Release Tablets, USP 50 mg, 100-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 62037-831-01

by Teva Pharmaceuticals USA

Reason: Failed dissolution specifications: Out-of-Specification dissolution test result obtained during routine stability testing.
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira, Inc., Lake Forest, IL 60045, USA. NDC carton: 0409-3506-01; NDC vial: 0409-3506-11

by Pfizer Inc.

Reason: Lack of assurance of sterility: loss of container integrity.
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Cidofovir injection 375 mg/mL (75 mg/mL) vial Injection, 5 mL vials, Rx Only, Mfg. By Emcure Pharmaceutical Ltd Hinjawadi, Pune, India, Mfg for: Heritage Pharmaceuticals Inc. UPC 323155216388, NDC 23155-216-31

by Heritage Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility: complaints received about dried powder on the outside of the bottle
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fluocinolone Acetonide Topical Solution, USP 0.01%, 60ml Bottle, Manufactured for: Lupin Pharmaceutical, Inc. Baltimore, MD 21202 Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873. NDC 43386-069-60

by LUPIN SOMERSET

Reason: Failed Impurities/Degradation Specifications:Out of specification result noticed for total impurities observed during stability analysis
Published: October 31, 2018
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Cyclosporine 1% Human Eye Drops, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-2776-92

by Westlab Pharmacy, Inc. dba Westlab Pharmacy

Reason: Lack of Process Controls
Published: October 31, 2018
Distribution: Nationwide

View recall →

Data last updated: September 24, 2026 ET

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.