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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.

37,271
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
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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.

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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 141–160 of 37,271 recalls

FDA Recall United States Ongoing2026 recordClass I

EURO FOODS GROUP USA NJ INC

Product
Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 pack…
Reason
The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
Published
September 16, 2026
Distribution
The adulterated product was distributed…

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FDA Recall United States Ongoing2026 recordClass I

EXOTIQUE FOODS CANADA

Product
Momchipz Gluten Free Veggie Chips Broccoli Florets & Caulifl…
Reason
Undeclared Wheat.
Published
September 16, 2026
Distribution
Product was sold in the U.S.

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FDA Recall United States Status not reported2026 record

Saratoga Potato Chips Issues Allergy Alert on Undeclared Soy in J. HIGGS Loaded Bacon and Cheddar Potato Chips

Reason
Saratoga Potato Chips of Fort Wayne, IN, is recalling two Best if USED BY codes of 7.75-ounce packages of J. HIGGS Loaded Bacon and Cheddar Potato Chips because they may contain undeclared soy allergen. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threateni
Published
September 16, 2026

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FDA Recall United States Status not reported2026 record

Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk

Reason
Gias Foods of New York, NY is recalling 2 Lots of bettergoods Authentic Italian Lemon Alfredo Fettuccine, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and ot
Published
September 15, 2026

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FDA Recall United States Status not reported2026 record

So Delicious Dairy Free® Issues Voluntary Recall of Salted Caramel Cluster Non-Dairy Frozen Dessert Pints Due to Potential Presence of Foreign Material

Reason
WHITE PLAINS, N.Y. and LOUISVILLE, Colo., September 15, 2026 – Danone USA is issuing a voluntary recall of So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints with best-by dates on and before April 3, 2028 due to the potential presence of foreign materials, such as small
Published
September 15, 2026

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FDA Recall United States Status not reported2026 record

Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce

Reason
KEASBEY, N.J. (Sept. 14, 2026) –Wakefern Food Corp. has voluntarily recalled select containers of Wholesome Pantry Organic Unsweetened Apple Sauce after routine FDA testing identified elevated patulin levels that exceed food safety limits and do not meet Wakefern's quality standards
Published
September 14, 2026

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FDA Recall United States Status not reported2026 record

A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil

Reason
Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients ma
Published
September 14, 2026

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FDA Recall United States Status not reported2026 record

Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese

Reason
Whole Foods Market of Austin, TX is recalling Fromagerie Coop de Mean Cabricharme cheese because the product contains egg lysozyme, an egg white protein, which is not declared on the product label. People who have an allergy or severe sensitivity to eggs run the risk of a serious or life-threateni
Published
September 11, 2026

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FDA Recall United States Status not reported2026 record

Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk

Reason
09/10/2026, Evergreen Fresh Sprouts LLC of Moyie Springs, IDAHO is recalling 215 cases (6/4oz bags per case) of Broccoli Sprouts, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly pe
Published
September 10, 2026

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FDA Recall Ongoing2026 recordClass I

Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090

by OPTIMAL BALANCE PHARMACY

Reason
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass I

0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03

by Baxter Healthcare Corporation

Reason
Presence of particulate matter: Particulates identified as fiberglass
Published
September 9, 2026
Distribution
Natonwide in the USA

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FDA Recall Ongoing2026 recordClass II

Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.

by Golden State Medical Supply Inc.

Reason
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass III

Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC#: 60687-481-21, (Individual Dose NDC: 60687-481-11).

by American Health Packaging

Reason
Labeling: Label Mix-up
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Prasugrel Tablets, USP, 10mg, Rx only, 30 Tablets in each bottle, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 0378-5186-93.

by MYLAN PHARMACEUTICALS INC

Reason
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass III

Revcovi (elapegademase-lvlr) Injection, 2.4mg/1.5mL (1.6 mg/mL), Single-Dose Vial, Rx Only, For Intramuscular Use Only, Mfd. by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-502-01

by Chiesi USA, Inc.

Reason
Failed Stability Specifications: Out of specification stability result for the protein concentration profile.
Published
September 9, 2026
Distribution
MO and TN

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FDA Recall Ongoing2026 recordClass II

2% Chlorhexidine Gluconate* Cloth, Non-sterile, 6 Disposable cloths, Sage Products LLC, 3909 Three Oaks Road, Cary, Illinois 60013. NDC: 53462-705-26

by Sage Products, LLC

Reason
Cross Contamination with Other Products
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zagreb, Croatia, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054, NDC 50111-560-01

by Teva Pharmaceuticals USA, Inc

Reason
Presence of Foreign Tablets/Capsules
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass III

Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-102-30.

by Supernus Pharmaceuticals, Inc.

Reason
Failed dissolution specifications.
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Carton label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, 4 Single Dose Vials, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505, Made in India, NDC 67457-386-81. Vial Label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, Single Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505, Made in India, NDC 67457-386-00.

by MYLAN PHARMACEUTICALS INC

Reason
Failed Dissolution Specifications
Published
September 9, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-6; UPC 8 50041 64004 4

by Lexia LLC

Reason
CGMP Deviations: Potential contamination of raw material
Published
September 9, 2026
Distribution
Distributed in the state of Colorado (US…

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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.

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