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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 14,801–14,820 of 18,563 recalls

FDA Recall Terminated Historical recordClass II

TNPRDC Injection, 6 mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

EDTA Calcium Disodium Injectable, 300mg/mL, 50mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Chromium Injectable, 200mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HCG (Lyophilized) Injectable, 5000 units/vial, 5mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Methylcobalamin Buffered Injectable, 5mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Phosphatidylcholine/Deoxycholic Acid Injection (Preserved) 50 ML 10/4.75%; Phosphatidylcholine/Deoxycholic Acid Injection (Preserved) 50 ML 5/2.5%; Phosphatidylcholine/Deoxycholic Acid Injection (Preserved) 50 ML 5/4.2%, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Cyanocobalamin Buffered Injectable 3mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Taurine Injectable, 50mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Methylcobalamin Buffered Injectable, 1mg/mL, packaged in a) 10mL vial, b) 30mL Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Vitamin D3 Injectable, 10,000 U/mL, 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Co-Enzyme Q-10 Injectable, 20mg/mL, 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Riboflavin-5-Phosphate Injectable,10mg/mL, 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

MICML TRNDPPC Injection (Preserved) 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ascorbic Acid Injectable 500mg/mL, packaged in a) 10mL vials, b) 50mL vials, c)100mL vials, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

EDTA Disodium Injectable, 150mg/mL, 100mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

L-Tyrosine Injectable, 25mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

L-Glutamine Injectable, 30mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435

by Downing Labs, LLC

Reason
Lack of Assurance of Sterility
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

KABOOM action strips, Sexual Performance Strips, packaged in 6.4oz box 12 strips per box, Nutrology USA LLC

by Blue Square Market, Inc.

Reason
Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG), capsules, packaged in 1.6oz box 30 capsules per box, Kunming Dali Industry & Trade Co., Ltd

by Blue Square Market, Inc.

Reason
Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine and Phenolphthalein.
Published
November 25, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Hydrocortisone and Acetic Acid Otic Solution, USP, containing hydrocortisone (1%) and acetic acid (2%), 10 mL bottles, Rx Only, Hi-Tech Pharmacal, Amityville, NY 11701, Made in USA, NDC # 50383-901-10

by Akorn, Inc.

Reason
Defective Container: Product missing safety seal around the neck of the bottle. The product label indicates, "Tamper Evident: Do not use if printed seal around cap is broken or missing." Because the product is missing the approved component and is not consistent with the labeling, the lot is being recalled.
Published
November 25, 2015
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.