Skip to main content
Get Alerts

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.

37,066
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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.

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 4,601–4,620 of 17,993 recalls

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Peanut Butter & Chocolate Filled Jumbo Cupcake. Product wer…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Grab & Go Apple & Celery Tray w/Peanut Butter. Product were…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Deli Snack Peanut Butter & Trail Mix Combo. Product were av…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Chocolate Peanut Butter Cup. Product were available for pur…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Celery & Peanut Butter Cup. Product were available for purc…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Apples Sliced With Peanut Butter. Product were available fo…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Mini Peanut Butter Cream Pie. Product was available for pur…
Reason
Potential Salmonella contamination.
Published
June 29, 2022
Distribution
The store prepared products were availab…

View recall →

FDA Recall United States Terminated Historical recordClass II

Taylor Farms Retail Inc

Product
Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz.…
Reason
Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains chopped roasted peanuts and peanut lime dressing.
Published
June 29, 2022
Distribution
U.S . distribution to the following: AL,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albanese Confectionery Group, Inc.

Product
Rich s Milk Chocolate Giant Layered Peanut Butter and Cups R…
Reason
Salmonella. Product made using recalled Jif peanut butter
Published
June 29, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434

by Walmart Inc

Reason
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.

by Walmart Inc

Reason
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass I

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.

by Walmart Inc

Reason
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Zileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 by Lupin Limited, Nagpur-441108, India, NDC 68180-169-16

by Lupin Pharmaceuticals Inc.

Reason
Failed Dissolution Specifications: Out of specification test results observed in dissolution testing during long term stability study.
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML plastic bottles; Premium Nature, South Plainfield, NJ. UPC 819192028668

by AMS Packaging Inc

Reason
Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 25 x 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC 16714-090-40 packaged in 25 count carton.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Lack of assurance of sterility
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Manufactured for: Northstart Rx LLC, Memphis, TN, 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC 16714-981-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Lack of assurance of sterility
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 62756-091-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Lack of assurance of sterility
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Lack of assurance of sterility
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by: Sun Pharmaceutical Industries, Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India Distributed by: Afaxys Pharma, LLC, Charleston, SC, 29403, USA, Product of Italy, NDC 50102-591-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Lack of assurance of sterility
Published
June 22, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Vaccinotoxinum, Potency: 32X, 11C, 30C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411

by Washington Homeopathic Products, Inc.

Reason
cGMP deviations
Published
June 22, 2022
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.