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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.

36,950
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/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 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 721–740 of 22,519 recalls

FDA Recall United States Terminated 2026 recordClass II

SAPUTO CHEESE USA, INC

Product
Great Value Cottage Cheese Small Curd 4% Milkfat NET WT 16oZ…
Reason
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated 2026 recordClass II

SAPUTO CHEESE USA, INC

Product
Great Value Lowfat Cottage Cheese Small Curd 2% Milkfat NET…
Reason
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated 2026 recordClass II

SAPUTO CHEESE USA, INC

Product
Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat NE…
Reason
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated 2026 recordClass II

SAPUTO CHEESE USA, INC

Product
CLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 1…
Reason
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated 2026 recordClass II

SAPUTO CHEESE USA, INC

Product
CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ…
Reason
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing 2026 recordClass III

Winder Laboratories, LLC

Product
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx…
Reason
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall Ongoing 2026 recordClass II

Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1592-7

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
Published
March 18, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

CNC Noodle Corporation

Product
Secondary Packaging: ZHONG HUA CHAO MIAN NOODLE INGREDIENTS:…
Reason
Undeclared wheat and Yellow #6.
Published
March 18, 2026
Distribution
U.S. Distribution: CA, NV. Foreign Distr…

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FDA Recall United States Ongoing 2026 recordClass II

CNC Noodle Corporation

Product
Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLO…
Reason
Undeclared wheat.
Published
March 18, 2026
Distribution
U.S. Distribution: CA, NV. Foreign Distr…

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FDA Recall United States Ongoing 2026 recordClass II

Palmetto Gourmet Foods Inc.

Product
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ing…
Reason
Product contains undeclared Yellow #5
Published
March 18, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing 2026 recordClass II

Palmetto Gourmet Foods Inc.

Product
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ing…
Reason
Product contains undeclared Yellow #5
Published
March 18, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing 2026 recordClass I

Ambrosia Brands LLC

Product
Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 cap…
Reason
Product may be contaminated with Salmonella
Published
March 18, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass III

Tipp Distributors, Inc. dba Novamex

Product
C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-0…
Reason
The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (5g per 17.5oz can), while the primary packaging (the can) has the correct Nutrition Facts Panel and Ingredient List.
Published
March 18, 2026
Distribution
Multiple states

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FDA Recall Ongoing 2026 recordClass II

Amnesteem (Isotretinoin) Capsules, USP 40 mg, packaged in 3 x 10-Count Prescription Packs, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV, 26505 USA, Made in France, NDC 0378-6614-93.

by MYLAN PHARMACEUTICALS INC

Reason
Failed Dissolution Specifications
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0

by Mohamed Hagar

Reason
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC 69208-003-15; Order 49317, 49323, 49325, 49329, 49333, 49339, 49341,49355, 49364, 49380, 49392. (b) 2 ml V-Vial, NDC 69208-003-25; Order 49353,49457, 49477. (c) 3 ml V-vial, NDC 69208-003-35; Order 49454,49406. Rx Only, Manufactured by: International Isotopes Inc., Idaho Falls, ID.

by Radnostix

Reason
Presence of Particulate Matter: Due to production issues
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

by ANTHONY TRINH, 123Herbals LLC

Reason
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.

by HTO Nevada Inc. dba Kirkman

Reason
Stability Data Does Not Support Expiry Date.
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.

by HTO Nevada Inc. dba Kirkman

Reason
Stability Data Does Not Support Expiry Date.
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.

by HTO Nevada Inc. dba Kirkman

Reason
Stability Data Does Not Support Expiry Date.
Published
March 11, 2026
Distribution
Nationwide

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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.