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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: AK ×
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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

PEPTIME Energy (caffeine 250mg) tablets, packaged in a) 6 count packets and b) 100-count bottles, Marketed by: DMD Pharmaceuticals, A Division of Dickery Consumer Products, Inc., Noblesville, IN 46060.

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

PEPTIME Energy (caffeine 350mg) tablets, packaged in a) 6 count packets and b) 100-count bottles, Marketed by: DMD Pharmaceuticals, A Division of Dickery Consumer Products, Inc., Noblesville, IN 46060.

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

PEPTIME Energy (caffeine 300mg) tablets, packaged in a) 6 count packets and b) 100-count bottles, Marketed by: DMD Pharmaceuticals, A Division of Dickery Consumer Products, Inc., Noblesville, IN 46060.

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

PEPTIME Energy (caffeine 250mg) tablets, 100-count bottles, Marketed by: DMD Pharmaceuticals, A Division of Dickery Consumer Products, Inc., Noblesville, IN 46060.

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

MAGNACAL (calcium carbonate 420 mg), 2 tablet packets, Manufactured for: Afassco Inc. Minden, NV 89423

by Ultra Seal Corporation

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

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FDA Recall Terminated Historical recordClass II

PAPENOL (acetaminophen 500 mg), 2 tablet packets, Manufactured for: Afassco Inc. Minden, NV 89423

by Ultra Seal Corporation

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

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FDA Recall Terminated Historical recordClass II

Regular Strength Pain Reliever (acetaminophen 110 mg, aspirin 162 mg, Caffeine 32.4 mg, Salicylamide 152 mg) 2 tablet packets, Mfg for Advanced First Aid, Baltimore, MD 21237, NDC 67060-0113-00

by Ultra Seal Corporation

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

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FDA Recall Terminated Historical recordClass II

Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets, Mfg for Advanced First Aid, Baltimore, MD 21237, NDC 67060-194-68

by Ultra Seal Corporation

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

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FDA Recall Terminated Historical recordClass II

Mint Flavored Antacid (Calcium Carbonate 420mg) 2 tablet packets, Mfg for Just American Safety, Osceola, IN 46561, NDC 67060-303-68

by Ultra Seal Corporation

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

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FDA Recall Terminated Historical recordClass II

CONGESTAID II Nasal Decongestant (Phenylephrine HCl 5mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC 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

PAINAID PMF Premenstrual Formula (acetaminophen 500 mg, pamabrom 25mg) 2 caplet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-0046-03

by Ultra Seal Corporation

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

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FDA Recall Terminated Historical recordClass II

PAINAID BRF Back Relief Formula (acetaminophen 250 mg, caffeine 50 mg, Magnesium salicylate 290 mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-0003-00

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

PAINAID (acetaminophen 110 mg, aspirin 162mg, caffeine 32.4 mg, salicylamide 152mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

EXTRA STRENGTH UN-ASPIRIN (acetaminophen 500 mg) 2 Caplet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-041-03

by Ultra Seal Corporation

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

View recall →

FDA Recall Terminated Historical recordClass II

DILOTAB II, SINUS AND COLD RELIEF NON DROWSY (acetaminophen 325 mg, Phenylephrine HCl 5 mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-052-03

by Ultra Seal Corporation

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

View recall →

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

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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

View recall →

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

View recall →

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

View recall →

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

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.