Skip to main content

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.

37,060
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
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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 1,341–1,360 of 19,636 recalls

FDA Recall United States Terminated Historical recordClass II

NuNaturals Inc

Product
Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187…
Reason
Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener.
Published
August 6, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

NuNaturals Inc

Product
Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Produ…
Reason
Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Published
August 6, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Moon N Sea GA LLC

Product
Yellow Fin Tuna, Net WT (variable weight) 50 lb brown corrug…
Reason
RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
Published
August 6, 2025
Distribution
Products were shipped to the following s…

View recall →

FDA Recall United States Terminated Historical recordClass II

Moon N Sea GA LLC

Product
Blue Fin Tuna, Net WT (variable weight) 50 lb brown corrugat…
Reason
RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
Published
August 6, 2025
Distribution
Products were shipped to the following s…

View recall →

FDA Recall United States Terminated Historical recordClass II

Moon N Sea GA LLC

Product
Fresh Scottish Salmon Fillet, Net WT (variable weight) 50 lb…
Reason
RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
Published
August 6, 2025
Distribution
Products were shipped to the following s…

View recall →

FDA Recall United States Terminated Historical recordClass II

Moon N Sea GA LLC

Product
Fresh Chilean Salmon Fillet, Net WT (variable weight) 50 lb…
Reason
RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
Published
August 6, 2025
Distribution
Products were shipped to the following s…

View recall →

FDA Recall United States Terminated Historical recordClass II

Camerican International Inc

Product
Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cre…
Reason
Undeclared Allergen (Milk). Consumer found a breaded halloumi Cheese Stick in the bag of churro bites. The Halloumi Cheese contains milk which is not an allergen in the churros.
Published
August 6, 2025
Distribution
The recalled product was distributed to…

View recall →

FDA Recall Ongoing Historical recordClass II

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton)

by Cipla USA, Inc.

Reason
Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
Published
July 30, 2025
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, Naples, Florida 34108, NDC# 68180-492-01

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry.
Published
July 30, 2025
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass III

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.

by Imprimis NJOF, LLC

Reason
Sub-Potent Drug: Subpotent assay results during stability testing.
Published
July 30, 2025
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01

by Imprimis NJOF, LLC

Reason
Sub-Potent Drug: Subpotent assay results during stability testing.
Published
July 30, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Mondelez Global Llc

Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 co…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

View recall →

FDA Recall United States Ongoing Historical recordClass II

Mondelez Global Llc

Product
Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20-…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

View recall →

FDA Recall United States Ongoing Historical recordClass II

Mondelez Global Llc

Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 c…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

View recall →

FDA Recall United States Ongoing Historical recordClass II

Mondelez Global Llc

Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 co…
Reason
Undeclared allergens (Peanut) due to mispackaging
Published
July 30, 2025
Distribution
The recalled product was distributed to…

View recall →

FDA Recall Ongoing Historical recordClass II

Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz./ 53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-040-00 UPC Code 815195018224

by A.P. Deauville, LLC

Reason
CGMP Deviations
Published
July 23, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Beauty & Skincare Power Stick original nourishing invisible protection roll-on Antiperspirant/Deodorant Spring Fresh, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-039-00, UPC Code 815195018194

by A.P. Deauville, LLC

Reason
CGMP Deviations
Published
July 23, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313

by A.P. Deauville, LLC

Reason
CGMP Deviations
Published
July 23, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Rizatriptan Benzoate Tablets, USP, 10 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877-262-18

by Ascend Laboratories, LLC

Reason
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Published
July 23, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Rizatriptan Benzoate Tablets, USP, 5 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877-261-18

by Ascend Laboratories, LLC

Reason
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Published
July 23, 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.