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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 October 2026.

37,212
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/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 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 19,781–19,800 of 20,558 recalls

FDA Recall Terminated Historical recordClass II

TL-DEX DM, Cough Suppressant Decongestant, Expectorant 16 fl oz. bottle, OTC, Manufactured for: Trigen Laboratories, Sayreville, NJ,08872, NDC 13811-067-16

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Mesehist WC, Antihistamine, Antitussive, Decongestant, 16 fl oz. bottle, OTC, Manufactured for: Trigen Laboratories, Sayreville, NJ,08872, NDC 13811-0075-16

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Mesehist DM, Antihistamine, Antitussive, Decongestant, 16 fl oz. bottle, OTC, Manufactured for: Trigen Laboratories, Sayreville, NJ,08872 NDC 13811-0085-16

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

CPM / PSE DM Drops, Antihistamine, Cough Suppressant Decongestant, 1 fl oz. bottle, OTC, Manufactured for: Trigen Laboratories, Sayreville, NJ,08872 NDC 13811-072-30

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

CPM / PSE Drops, Antihistamine, Nasal Decongestant, 1 fl oz. bottle, OTC, Manufactured for: Trigen Laboratories, Sayreville, NJ,08872, NDC 13811-071-30

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

TG 40PSE/400GFN Tablets, 1000 count bottle, OTC Manufactured by: TG United, Inc. Brooksville, FL 34604 NDC 29273-0706-10

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Poly-Vent IR, Poly-Vent DM Tablets, Expectorant, Nasal Decongestant, 60 count bottle, OTC, Distributed by: Poly Pharmaceuticals, Quitman, MS 39355, NDC 50991-561-60

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Poly-Vent DM Tablets, Cough Suppressant, Expectorant, Nasal Decongestant, 60 count bottle, OTC, Distributed by: Poly Pharmaceuticals, Quitman, MS 39355 NDC 50991-309-60

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Poly Hist Forte, Nasal Decongestant, Antihistamine, 100 count bottle, OTC, Manufactured for: Poly Pharmaceuticals, Quitman, MS 39355 NDC 50991-210-01

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Lusair Liquid, 1 PINT bottle, OTC, Marketed by: Pernix Therapeutics, Gonzales, LA 70737 NDC 23359-017-16

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

BroveX PSB DM LIQUID, Antihistamine, Decongestant, a) 16 fl oz. bottle, OTC, NDC 58605-151-01 b) 20 ml NDC 58605-151-02, Manufactured for: Pernix Therapeutics, Gonzales, LA 70737

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

BroveX PSB LIQUID, Antihistamine, Decongestant, a) 16 fl oz. bottle, OTC, NDC 58605-150-01 b) 20 ml NDC 58605-150-02, Manufactured for: Pernix Therapeutics, Gonzales, LA 70737

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

BroveX PSE DM, Antihistamine, Cough Suppressant, Decongestant, 100 count bottle, OTC, Manufactured for: Pernix Therapeutics, Gonzales, LA 70737 NDC 58605-441-01

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

BroveX PSE, Antihistamine, Nasal Decongestant, 100 count bottle, OTC, Manufactured for: Pernix Therapeutics, Gonzales, LA 70737 NDC 58605-440-01

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Maxifed-G, Expectorant, Nasal Decongestant, 100 count bottle, OTC, Manufactured for: MCR American Pharmaceuticals Inc. Brooksville, FL 34604, NDC 58605-0408-01

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Maxifed DM, Expectorant, Nasal Decongestant, 100 count bottle, OTC, Manufactured for: MCR American Pharmaceuticals Inc. , Brooksville, FL 34604, NDC 58605-0409-01

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Cardec DM Drops, Decongestant, Antihistamine, Antitussive, 1 fl oz. bottle, OTC, Manufactured for: Macoven Pharmaceuticals, Magnolia, TX 77354 NDC 44183-550-30

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Cardec Drops,Antihistamine, Nasal Decongestant, 1 fl oz. bottle, OTC, Manufactured for: Macoven Pharmaceuticals, Magnolia, TX 77354 NDC 44183-604-30

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

BROMPHENIRAMINE/PSEUDOEPHEDRINE DM, LIQUID, Antihistamine, Cough Suppressant, Decongestant, 16 fl oz. bottle, OTC, Manufactured for: Macoven Pharmaceuticals, Magnolia, TX 77354 NDC 44183-311-16

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

View recall →

FDA Recall Terminated Historical recordClass II

Dallergy CHEWABLE TABLETS, Antihistamine, Nasal Decongestant, 100 count bottle, OTC, Manufactured for: Laser Pharmaceuticals, LLC, Greenville, SC 29615, NDC 16477-152-01

by TG United, Inc.

Reason
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Published
June 12, 2013
Distribution
FL, MS, SC, LA and TX

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.