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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.

37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • Oct 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,881–14,900 of 21,652 recalls

FDA Recall United States Terminated Historical recordClass I

Severn Peanut Co., Inc. DBA Hampton Farms

Product
Avas 8 oz. Organic Roasted Unsalted Cashews UPC 8-10111-0103…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
July 5, 2017
Distribution
Direct to one consignee in NJ. Further…

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FDA Recall United States Terminated Historical recordClass I

Severn Peanut Co., Inc. DBA Hampton Farms

Product
Ava's brand Organic Cashews Roasted & Salted 8 oz. tubs, UPC…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
July 5, 2017
Distribution
Direct to one consignee in NJ. Further…

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FDA Recall Terminated Historical recordClass II

Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc. Eden Prairie, MN 55344

by Vi-Jon, Inc.

Reason
Presence of foreign substance: glass particle
Published
June 28, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.

by Lucid Pharma LLC

Reason
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Published
June 28, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Montelukast Sodium Oral Granules, 4 mg pouch, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-6040-93

by Mylan Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications; out of specification results for Sulphoxide Impurity and Total Impurities
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

by Complete Pharmacy and Medical Solutions LLC

Reason
Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP, Service Code 2K2227, NDC# 61553-027-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.75g in 300 mL 0.9% Sodium Chloride Injection USP, Service Code 2K2237, NDC# 61553-037-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.5g in 300 mL 0.9% Sodium Chloride Injection USP, Service Code 2K2243, NDC# 61553-043-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 7 mMol 100 mL Bag, Service Code 2K5284, NDC# 61553-0284-48, Total Volume 100.00 mL incorrectly labeled as 102.33 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 20 mMol 100 mL Bag, Service Code 2K5287, NDC# 61553-0287-48, Total Volume 100.00 mL incorrectly labeled as106.67 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 10 mMol 100 mL Bag, Service Code 2K5288, NDC# 61553-0288-48, Total Volume 100.00 mL incorrectly labeled as 103.33 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 15 mMol 100 mL Bag, Service Code 2K5295, NDC# 61553-0295-48, Total Volume 100.00 mL incorrectly labeled as105.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium PHOSphate added to 0.9% Sodium Chloride, 7.5 mMol 100 mL Bag, Service Code 2K5298, NDC# 61553-0298-48, Total Volume 100.00 mL incorrectly labeled as 102.50 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium PHOSphate in 0.5% Dextrose, 7.5 mMol in 100 mL, Service Code 2K5299, NDC# 61553-0299-48, Total Volume 100.00 mL incorrectly labeled as 150.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium CHLORide added to 0.9% Sodium Chloride, 10mEq 100 mL Bag, Service Code 2K5856, NDC# 61553-0856-48, Total Volume 100.00 mL incorrectly labeled as 105.00 mL, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Potassium CHLORide added to 0.9% Sodium Chloride, 30mEq 100 mL Bag, Service Code 2K5824, NDC# 61553-0824-48, Total Volume 100.00 mL incorrectly labeled as 115.00 mL, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

NasalCrom (cromolyn sodium) Nasal Spray, USP, 5.2 mg per spray, 200 metered sprays, 0.88 FL OZ (26 mL) metered spray pump bottle, Distributed by: Medtech Products, Inc., Tarrytown, NY 10591, UPC 8 148332 01101 7.

by Bausch & Lomb, Inc.

Reason
CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04

by Hospira Inc., A Pfizer Company

Reason
GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

GLOBAL COMMODITIES INC

Product
AAHU BARAH, DRY FIG, NET WT. 1 LB, PRODUCT OF PAKISTAN
Reason
Presence of Undeclared Sulfites
Published
June 21, 2017
Distribution
NY, NJ, MA & VA

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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.