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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.

37,066
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 2,781–2,800 of 21,105 recalls

FDA Recall Terminated Historical recordClass II

fentaNYL 100 mcg/50 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 50 mL Injection (fentaNYL Concentration = 2 mcg/mL), EPIDURAL USE ONLY, 50 mL fill Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd, Windsor, CT 06095, NDC 70004-0231-22, Bar Code 70004023122

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 200 mcg/100 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 100 mL Injection, (fentaNYL Concentration = 2 mcg/mL), EPIDURAL USE ONLY, 100 mL Yellow CADD Cassette, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0231-64, Bar Code 70004023164

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 200 mcg/100 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 100 mL Injection (fentaNYL Concentration = 2 mcg/mL), EPIDURAL USE ONLY, 100 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0231-32, Bar Code 70004023132

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/50 mL Injection (Concentration = 50 mcg/mL), INTRAVENOUS USE ONLY, 50 mL Bag, Rx only, SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0222-30 BAR code 70004022230

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/250 mL in 0.9% Sodium Chloride Injection (Concentration = 10 mcg/mL), 250 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, 877.550.5059, NDC 70004-0229-40 BAR code 70004022940

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Diltiazem HCl 125 mg in 0.9% Sodium Chloride Injection (Concentration = 1mg/mL), 125 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095; NDC 70004-0541-35, Bar Code 70004054135

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Roland Foods, LLC.

Product
Roland Tahini; 100% Ground Sesame Seeds; Net WT. 16 OZ. (1 L…
Reason
Product may be contaminated with Salmonella.
Published
April 3, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Otis McAllister

Product
Product LAbeled in part: "Emerald River Premium Thai Jasmine…
Reason
Foreign object; piece of glass.
Published
April 3, 2024
Distribution
U.S. distribution to the following: UT,…

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FDA Recall United States Terminated Historical recordClass I

Wenders LLC

Product
Trader Joe's 50% Less Sodium Roasted & Salted Whole Cashews…
Reason
Potential contamination with Salmonella.
Published
April 3, 2024
Distribution
U.S. distribution: CA, WA, TX No foreig…

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FDA Recall United States Terminated Historical recordClass II

Barsotti Juice Company, Inc.

Product
Barsotti Organic Carrot Juice 16 oz. and 64 oz. plastic bott…
Reason
Product was determined to be under processed.
Published
April 3, 2024
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass II

WS Global Inc

Product
Himalayan Pain Relief Tea for Gout and Hangover
Reason
Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Published
April 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.

by Super Chill Products

Reason
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01

by Hikma Pharmaceuticals USA Inc.

Reason
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Nicardipine Hydrochloride Injection, USP 25mg/mL (2.5 mg/mL) 10 mL vials, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520, NDC 55150-183-11

by Eugia US LLC

Reason
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Nicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per 10mL, 10mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 NDC 55150-183-10

by Eugia US LLC

Reason
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Digoxin Tablets, USP 125mcg, (0.125 mg), 1000-count bottle, Rx Only, Manufactured by: Novitium Pharma LLC., 70 Lake Drive, East Windsor, New Jersey 08520, NDC 70954-201-20

by Novitium Pharma LLC

Reason
Cross Contamination with Other Products:(mycophenolate mofetil).
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

la fiesta food products

Product
La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), U…
Reason
Elevated levels of lead found in product
Published
March 27, 2024
Distribution
U.S. distribution to 319 retailers in Ca…

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FDA Recall United States Terminated Historical recordClass I

Reser's Fine Foods, Inc.

Product
Item 404764, KIT EM CHICKEN STREET TACO DP EXPRESS MEAL 6/22…
Reason
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Published
March 27, 2024
Distribution
Distributed in CA, CT, FL, ID, IL, MD, M…

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FDA Recall United States Terminated Historical recordClass I

Reser's Fine Foods, Inc.

Product
FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap…
Reason
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Published
March 27, 2024
Distribution
Distributed in CA, CT, FL, ID, IL, MD, M…

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FDA Recall United States Terminated Historical recordClass I

Reser's Fine Foods, Inc.

Product
FCF Item 403953, HEB Poblano Caesar Dressing, 12oz. glass bo…
Reason
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Published
March 27, 2024
Distribution
Distributed in CA, CT, FL, ID, IL, MD, M…

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.