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 October 2026.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 3,081–3,100 of 19,443 recalls

FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass I

Cookies-n-Milk Incorporated

Product
Edible Cookie Dough Chocolate Chip packaged in 6 oz plastic…
Reason
Undeclared Peanut Butter; Packaged Peanut Butter Dough in Chocolate Chip packaging.
Published
November 15, 2023
Distribution
Product is sold retail in Convenience st…

View recall →

FDA Recall TerminatedTerminated: August 16, 2024Historical recordClass III

Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 5mg/6.25mg, 100-count Bottle, RX only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC 68462-879-01

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Impurities/Degradation Specifications
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: July 25, 2024Historical recordClass II

Liothyronine Sodium Tablets, USP, 25 mcg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc.Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191,(U.T. of D & NH), India. NDC 62756-590-88

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Impurities/Degradation Specifications.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: July 25, 2024Historical recordClass II

Liothyronine Sodium Tablets, USP, 5 mcg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc.Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191,(U.T. of D & NH), India. NDC 62756-589-88

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Impurities/Degradation Specifications.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 8, 2024Historical recordClass II

Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%), 14 mL Glass Dropper bottle in box, RX only, Safecor Health, LLC, Woburn, MA 01801. NDC# 48433-230-15

by Safecor Health, LLC

Reason
CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Gynazole-1, (Butoconazole Nitrate) Vaginal Cream USP, 2%, Net Wt 5.8 g per pre-filled applicator, packaged in 1 prefilled applicator per carton, Rx Only, Manufactured By Padagis, Yeruham, Israel; Distributed By: Padagis, Allegan, MI 49010. NDC: 45802-396-01

by Padagis US LLC

Reason
Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to manufacture the product rather than Hydrophobic Colloidal Silica as required by the manufacturing process.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 16, 2024Historical recordClass III

Opium Tincture, USP (Deodorized), 10 mg/mL of anhydrous morphine, packaged in 118 mL (4 Fl oz) bottles, Rx only, Manufactured for: Edenbridge Pharmaceuticals, LLC Parsippany, NJ 07054, NDC 42799-217-01

by Edenbridge Pharmaceuticals, LLC

Reason
Subpotent Drug
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, chewable tablets, 72-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0118-83, UPC 3-0766-0746-50-8

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets, packaged in 265-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 135-0181-05, UPC 3-0766-3072-14-7

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets, packaged in 12-count roll, Dist. by: GSK CH, Warren, NJ 07059. NDC: 135-0181-03, UPC 3-0766-0746-70-6

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets, packaged in 72-count bottles, Dist. by: GSK CH, Warren, NJ 07059. NDC: 135-0181-02, UPC 3-0766-0746-50-8

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Fruit flavor, Chewable Tablets, packaged in 160-count bottles, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0118-14, UPC 3-0766-0746-10-2

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, packaged in 12-count roll, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0228-01, UPC 3-0766-0746-80-5

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass II

TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 0135-0228-06, UPC 3-0766-0745-85-3

by GlaxoSmithKline Consumer Healthcare Holdings LLC

Reason
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 12, 2024Historical recordClass II

Select Custom Solutions, LLC

Product
JayRobb Vanilla Flavored Egg White Protein Powder. Net Weig…
Reason
foreign material - plastic
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass I

Braga Fresh Foods

Product
Wegman's Organics Sweet Kale Chopped Salad Kit, 8oz.
Reason
Undeclared egg
Published
November 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 15, 2024Historical recordClass III

VANCOmycin HCI PF, 1.5 g added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-029-68.

by Denver Solutions, LLC DBA Leiters Health

Reason
Labeling: Not Elsewhere Classified
Published
November 1, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 15, 2024Historical recordClass III

VANCOmycin HCI PF, 1.25 g added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-028-68.

by Denver Solutions, LLC DBA Leiters Health

Reason
Labeling: Not Elsewhere Classified
Published
November 1, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 15, 2024Historical recordClass III

Oxytocin synthetic, 30 Units added to 0.9% Sodium Chloride 500mL IV Bag (0.06 Units per mL), Rx only, Leiter Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-157-70

by Denver Solutions, LLC DBA Leiters Health

Reason
Labeling: Not Elsewhere Classified
Published
November 1, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: July 10, 2024Historical recordClass II

Restore Sinus Spray, Manufactured by: Biomic Sciences, LLC Charlottesville, VA

by Biomic Sciences, LLC dba ION Intelligence of Nature

Reason
Microbial contamination of Non-Sterile Products
Published
November 1, 2023
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.

Reconnecting to the server…

We lost the connection to the server.

Your session has expired.