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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.

37,059
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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 2,072 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)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 741–760 of 21,591 recalls

FDA Recall United States Terminated 2026 recordClass II

Wawa Beverage Company

Product
Wawa Cookies & Cream Milk 16 oz (Pint), Plastic bottle Store…
Reason
Foreign plastic material discovered on fill line.
Published
March 25, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Terminated 2026 recordClass II

Wawa Beverage Company

Product
Wawa Double Dutch Chocolate Milk ,16 oz (Pint) Plastic bottl…
Reason
Foreign plastic material discovered on fill line.
Published
March 25, 2026
Distribution
The recalled product was distributed to…

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FDA Recall United States Terminated 2026 recordClass II

Wawa Beverage Company

Product
Wawa Reduced Fat Milk 2% 16 oz (Pint)
Reason
Foreign plastic material discovered on fill line.
Published
March 25, 2026
Distribution
The recalled product was distributed to…

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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

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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FDA Recall Ongoing 2026 recordClass II

Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Country of origin: Taiwan, NDC 16571-816-51.

by Rising Pharma Holding, Inc.

Reason
Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6818-06.

by The Harvard Drug Group LLC

Reason
Defective container; inadequately sealed blister packaging.
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, Outer carton: 112 capsules (4 individual packs containing 28 capsules each), NDC 69097-032-74; Inner carton: 28 capsules (4 blisters of 7 capsules), NDC 69097-032-56; Foil blister: NDC 69097-032-17

by Cipla USA, Inc.

Reason
Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
Published
March 11, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Nilotinib Capsules, 150 mg per capsule, packaged in cartons, Rx only, Manufactured by: Cipla Ltd., Verna, Goa, India, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, Outer carton: 112 capsules (4 individual packs containing 28 capsules each) NDC 69097-031-74; Inner carton: 28 capsules (4 blisters of 7 capsules) NDC 69097-031-56; Foil blister: NDC 69097-031-17

by Cipla USA, Inc.

Reason
Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
Published
March 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.