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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 October 2026.

37,268
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.

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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)

  • 1,739 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 381–400 of 19,375 recalls

FDA Recall Ongoing2026 recordClass II

Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL), Manufactured for Burkhart Dental Supply, Tacoma, Washington, 98409. NDC: 43498-310-30

by Keystone Industries

Reason
Defective container:may contain bottles with incomplete seals
Published
June 24, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed by Dental Health Products, Inc, 2614 North Sugar Bush Road, New Franken, WI 54229. NDC 69634-020-30

by Keystone Industries

Reason
Defective container:may contain bottles with incomplete seals
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavor Net Contents: 1 oz (30 g), Quala Dental Products, Made in USA for NDC Inc., 407 Sanford Road, Le Vergne, TN 37086, NDC 43128-034-30.

by Keystone Industries

Reason
Defective container:may contain bottles with incomplete seals
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pearson Dental Supply Inc., Sylmar, CA 91342 USA, NDC 43305-0009-3.

by Keystone Industries

Reason
Defective container:may contain bottles with incomplete seals
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx Only, For Intramuscular or Intravenous use, Manufactured for: Endo USA, Malvern, PA 19355, NDC 42023-179-05

by Par Health USA, LLC

Reason
Crystallization; identified as Buprenorphine free base
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-056-03.

by Ajanta Pharma USA Inc

Reason
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC. 3650 Victoria St N, Suite 900, Shoreview, MN, NDC 71139-0190-1.

by IntegraDose Compounding Services LLC

Reason
Subpotent Drug
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in 240 mL (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-08.

by PAI Holdings LLC

Reason
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.

by PAI Holdings LLC

Reason
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Published
June 24, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.

by PAI Holdings LLC

Reason
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Published
June 24, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-04.

by PAI Holdings LLC

Reason
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Published
June 24, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, 0.5mg/0.035mg, 0.75mg/0.035mg, 1 mg/0.0.35mg, 3 Blister Cards each containing 28 tablets, 28 day regimen, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403 513, India, Manufactured for: Glenmark Pharmaceuticals Inc., Mahwah, NJ 07430, NDC 68462-556-29

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 3, 20262026 recordClass II

International Food Products Corporation

Product
Dairy House Ingredient Systems Strawberry Dairy Powder 05#50…
Reason
Potential for Salmonella
Published
June 24, 2026
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: September 3, 20262026 recordClass II

International Food Products Corporation

Product
Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb b…
Reason
Potential for Salmonella
Published
June 24, 2026
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: September 3, 20262026 recordClass II

International Food Products Corporation

Product
Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags
Reason
Product tested positive for Salmonella
Published
June 24, 2026
Distribution
Multiple states

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FDA Recall United States Completed2026 recordClass II

United States Bakery

Product
Great Value Hawaiian Roll 4pk, Item # F63384. Product is per…
Reason
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
Published
June 24, 2026
Distribution
Distributed in AL, AR, AZ, CA, FL, GA, I…

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FDA Recall United States Ongoing2026 recordClass II

Nutrisystem Inc

Product
Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow…
Reason
Undeclared Allergen (Soy)
Published
June 24, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Completed2026 recordClass III

Wild Coast Brew LLC

Product
The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.…
Reason
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
Published
June 17, 2026
Distribution
Nationwide

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FDA Recall United States Completed2026 recordClass III

Wild Coast Brew LLC

Product
The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net w…
Reason
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
Published
June 17, 2026
Distribution
Nationwide

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FDA Recall United States Completed2026 recordClass III

Wild Coast Brew LLC

Product
The Shadow Loose-Leaf Tea - Winter Spice Black Tea, net wt.…
Reason
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
Published
June 17, 2026
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.