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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 81–100 of 17,260 recalls

FDA Recall Ongoing 2026 recordClass II

CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.); b) Kit (1 BULB, Syringe & Drops- NDC 51316-823-00.), Distributed by: CVS Pharmacy., Inc. One CVS Drive, Woonsocket, RI 02895,

by Bell Pharmaceuticals, Inc

Reason
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published
July 22, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham, Israel, NDC 45802-059-35

by Padagis US LLC

Reason
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
Published
July 22, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Intravenous Use, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0857-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana Llana Rio Piedras, PR 00924, UPC 659685696567.

by Gasco Industrial Corp.

Reason
Subpotent drug
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 16 oz, 474 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana LLana Rio Piedras, PR 00924, UPC 69685696529

by Gasco Industrial Corp.

Reason
Subpotent drug
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 1 gallon (3.78 liter), Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana LLana Rio Piedras, PR 00924

by Gasco Industrial Corp.

Reason
Subpotent drug
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UPC 7 87302 12363 6.

by Gasco Industrial Corp.

Reason
Subpotent drug
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial Corp., PO Box 1360, Gurabo, PR 00778, Made in USA

by Gasco Industrial Corp.

Reason
Subpotent drug
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Gasco Isopropyl Alcohol 70%, Net Contents: 16 Oz. (474 mL). Manufactured by: Gasco Industrial Corp., PO Box 1360 Gurabo PR 00778 Made in USA UPC 7 87302 13044 3

by Gasco Industrial Corp.

Reason
Subpotent drug
Published
July 15, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, Product code: 70092-1310-46.

by QuVa Pharma, Inc.

Reason
Failed Impurities/Degradation Specifications
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 80090 2 FL OZ (59 mL) NDC 53329-159-13 4 FL OZ (118 mL) NDC 53329-159-04

by BioMed Laboratories, LLC.

Reason
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSource Specialty, Pharma Limited, Bengaluru - 561 203, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-893-31

by ONESOURCE SPECIALTY PHARMA LIMITED

Reason
Failed Impurities/Degradation Specifications
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Lehi Valley Trading Company, Inc

Product
High Valley Orchard Chocolate Covered Raisins, net wt. 15oz.…
Reason
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur - 441108, INDIA, NDC 70748-311-01

by Lupin Pharmaceuticals Inc.

Reason
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Published
July 8, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Gemcitabine Injection, 1 g per 26.3 mL (38 mg/mL), 26.3 mL Single-Dose Vial, For Intravenous Infusion ONLY, Rx only, Manufactured by: THYMOORGAN PHARMAZIE GmbH, Schiffgraben 23, 38690 Goslar, Germany; Distributed by: Hikma, Berkeley Heights, NJ 07922. NDC: 0143-9341-01

by McKesson

Reason
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
Published
July 8, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist cap, NDC 63347-120-01; Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670,

by Blaine Labs Inc

Reason
CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated
Published
July 8, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Undecylenic Acid) and 1x1oz bottle of Fungal Fusion Eradication Antimicrobial Show Spray (isopropyl Alcohol, D-Limonene, Undecylenic Acid). Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670, Manufactured for Doctor's Inc

by Blaine Labs Inc

Reason
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Published
July 8, 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.