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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

State: MP ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 14, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

SINU-PHEN PLUS sinus pain and congestion tabs (acetaminophen 500 mg, Phenylephrine HCl 5.0 mg) 2 tablet packets, Manufactured for: Tellus Medical Products, Palm Desert, CA 92211, NDC 69103-2536-00

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

PAIN TERMINATOR extra strength pain relief (aspirin 162 mg, acetaminophen 110 mg, Caffeine 32.4mg, Salicylamide 152 mg) 2 tablet packets, Manufactured for: Tellus Medical Products, Palm Desert, CA 92211, NDC 69103-2507

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5.0 Phenylephrine HCl) 2 tablet packets, Manufactured for: Tellus Medical Products, Carlsbad, CA 92011, NDC 69103-2556

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cold/Sinus Pain Reliever/Fever Reducer Nasal Decongestant (acetaminophen 325 mg, Phenylephrine HCl 5mg), 2 tablets per packet, Mfg, for Respond Industries and American First Aid, Mason, OH 45040

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Pain Away Pain Reliever/Fever Reducer (NSAID) (acetaminophen 110 mg, aspirin 162 mg, salicylamide 152mg, caffeine 32.4 mg), 2 tablets per packet, Mfg, for Respond Industries and American First Aid, Mason, OH 45040

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Headache & Congestion Sinus Relief (acetaminophen 250 mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-0206-02

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cold Relief (acetaminophen 250 mg, guaifenesin 200mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-112-03

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg, caffeine 50 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-111-832

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg), 2- tablet packets, Mfd. for First Aid Direct, Mason, OH 45040

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cold Relief Severe Pain/Cough (acetaminophen 325mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, phenylephrine HCl 5mg), 2-tablet packets, Manufactured for Select Corporation, Carrollton, TX 75007

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lite Remfresh Advanced Ion-Powered Melatonin (Melatonin 0.5mg) Tablets, 36-count blisters, Physician's Seal LLC, Boca Raton, FL 33487

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Multi Symptom Cold Relief (acetaminophen 325 mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) tablets, 2-count packets, Dist. by Honeywell Safety Products USA, Smithfield, RI 02917

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cetafen Non-aspirin pain reliever (acetaminophen 325mg) tablets, 2-count packets, Manufactured for: HARTHealth Seattle, WA 98124

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Back Pain-Off (caffeine 50mg, magnesium salicylate 290mg) Tablets 2-count packets, Mfd for MEDIQUE PRODUCTS, Fort Myers, FL 33967, NDC 47682-073-00

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MidNite Sleep Health (melatonin 1.5 mg) tablets, 30-count bottles, Distributed by: Mylan Consumer Healthcare, Inc. Morgantown, WV 26505 USA

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dologen (acetaminophen 325 mg and dexbrompheniramine maleate 1mg) caplets, packaged in a) 90-count bottles, b) 2-count packets, Manufactured in the USA for Kramer-Novis, San Juan, Puerto Rico 00917, NDC 52083-482-02

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ephedrine Plus (Ephedrine HCl 25mg, Guaifenesin 200mg) tablets, 24-count bottles, Marketed by: DMD Pharmaceuticals A Division of Dickery Consumer Products, Inc. Noblesville, IN 46060, NDC 65193-320-24

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

DBI 357 Super Magnum Quick Energy Stimulant (caffeine 200mg) tablets, packaged in a) 36-count bottles, b) 100-count bottles, c) 500-count bottles, and d) 3-count packets, Marketed by: DBI Distribution A Division of King Richard Promotions, Inc. P.O. Box 78546, Indianapolis, IN 46270

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cystex Urinary Pan Relief (NSAID) (methenamine 162mg, sodium salicylate 162.5mg tablets) packaged in a) 40-count blisters and b) 20-count blisters, Distributed by: Clarion Brands, LLC 27070 Miles Road, Suite A Solon, OH 44139, NDC 69693-512-40

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500 mg, diphenhydramine HCl 50mg caplets) 50-count bottles, Manufactured for: Church & Dwight Co., Inc. Ewing, NJ 08628 NDC 10237-907-50

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

View recall →

Data last updated: September 14, 2026 ET

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.