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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 September 2026.

36,949
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-riskPublished September 4, 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)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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 II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 641–660 of 18,300 recalls

FDA Recall Ongoing 2026 recordClass II

ESTRADIOL, 12.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79599-3012-32.

by F.H. INVESTMENTS, Inc. (dba Asteria Health)

Reason
Presence of Foreign substance - potential presence of metal particulate matter
Published
February 18, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

ESTRADIOL, 10 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3010-32.

by F.H. INVESTMENTS, Inc. (dba Asteria Health)

Reason
Presence of Foreign substance - potential presence of metal particulate matter
Published
February 18, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

ESTRADIOL, 6 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3006-32.

by F.H. INVESTMENTS, Inc. (dba Asteria Health)

Reason
Presence of Foreign substance - potential presence of metal particulate matter
Published
February 18, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10.

by Unichem Pharmaceuticals USA Inc.

Reason
Tablets/Capsules Imprinted with Wrong ID
Published
February 18, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-11

by Pro Numb Tattoo Numbing Spray LLC

Reason
cGMP deviations
Published
February 18, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11

by Pro Numb Tattoo Numbing Spray LLC

Reason
cGMP deviations
Published
February 18, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Diclofenac Sodium, Topical Gel, 3%, 100 g tube, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-1363-7

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-231-01.

by Granules Pharmaceuticals Inc.

Reason
Presence of Foreign Tablets/Capsules
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660

by Green Lumber Holdings, LLC

Reason
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIS LTD., Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India, Manufactured for: UNICHEM PHARMACEUTICALS (USA), INC., East Brunswick, NJ 08816, NDC 29300-187-01

by Unichem Pharmaceuticals USA Inc.

Reason
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

B.C. Williams Bakery Service, Inc

Product
Swiss Chocolate Cake Mix; 50 lb. multi-wall, kraft, poly-lin…
Reason
Undeclared Milk Allergen
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

B.C. Williams Bakery Service, Inc

Product
Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moi…
Reason
Undeclared Milk Allergen
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

B.C. Williams Bakery Service, Inc

Product
Spice Cake Mix; 50 lb. multi-wall, kraft, poly-lined moistur…
Reason
Undeclared Milk Allergen
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Imu-Tek Animal Health, Incorporated

Product
Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Die…
Reason
Undeclared milk allergen
Published
February 11, 2026
Distribution
Distributed in : AZ, CA, CO, FL, MA, ME,…

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FDA Recall United States Terminated 2026 recordClass I

VH FOODS INC

Product
Bread Crumbs, Outside The Breadbox brand, net wt. 8 oz, UPC…
Reason
Undeclared allergens: egg and milk
Published
February 11, 2026
Distribution
Distributed to the following states: CO,…

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FDA Recall United States Ongoing 2026 recordClass II

Diva Fam Inc

Product
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
Reason
potential Clostridium botulinum contamination
Published
February 11, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Diva Fam Inc

Product
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
Reason
potential Clostridium botulinum contamination
Published
February 11, 2026
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing 2026 recordClass II

Diva Fam Inc

Product
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
Reason
potential Clostridium botulinum contamination
Published
February 11, 2026
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing 2026 recordClass II

Diva Fam Inc

Product
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
Reason
potential Clostridium botulinum contamination
Published
February 11, 2026
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing 2026 recordClass II

Diva Fam Inc

Product
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
Reason
potential Clostridium botulinum contamination
Published
February 11, 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.