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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 11, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: N-desmethylsibutramine, benzylsibutramine, and sibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Magic Slim capsules, supplied in 60 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: N-desmethylsibutramine, benzylsibutramine, and sibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Slim Xtreme Weight loss capsules, 500 mg, supplied in 30 count bottles, Another product from Globe All Wellness, LLC Hollywood, FL 33020, distributed by MyNicKnaxs, LLC Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredient: N-desmethylsibutramine, benzylsibutramine, and sibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Meizi Evolution Soft Gel Capsules, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredient: N-desmethylsibutramine, benzylsibutramine, and sibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

SlimEasy Herbs Capsule, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredient: sibutramine and N-desmethylsibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Pill for weight reduction, (Japanese Chinese Formula from Japan Hokkaido Cangye Pharmacy Co, Ltd) 400 mg, supplied in 40 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredient: Phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Super Fat Burning Bomb Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: Phenolphthalein and N-desmethylsibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

Fruta BIO 400 mg capsules, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: Sibutramine and Phenolphthalein .
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

JIANFEIJINDAN Activity Girl Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared ingredient: N-di-desmethylsibutramine, an analog of sibutramine
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 2, 2019Historical recordClass I

REDUCE WEIGHT FRUTA PLANTA Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC., Deltona, FL

by MyNicNaxs, Inc.

Reason: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredient: Phenolphthalein.
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 7, 2016Historical recordClass I

Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

by Pure Edge Nutrition

Reason: Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 7, 2016Historical recordClass I

Bella Vi INSANE AMP'D Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

by Pure Edge Nutrition

Reason: Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 7, 2016Historical recordClass I

Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules, 30 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

by Pure Edge Nutrition

Reason: Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 7, 2016Historical recordClass I

Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules, 30 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

by Pure Edge Nutrition

Reason: Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 7, 2016Historical recordClass I

Bella Vi BTrim MAX Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

by Pure Edge Nutrition

Reason: Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 7, 2016Historical recordClass I

Bella Vi INSANE Bee Pollen Dietary Supplement Capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

by Pure Edge Nutrition

Reason: Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 12, 2014Historical recordClass I

vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.

by Vitality Research Labs LLC

Reason: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared vardenafil and tadalafil in vitaliKOR capsules
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 10, 2017Historical recordClass I

Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0182-2, UPC 3 59762-0182-2 9.

by Greenstone Llc

Reason: Presence of Foreign Tablets/Capsules: report of a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule was found in a bottle of Effexor XR (venlafaxine HCl) 150 mg capsules that was packaged in the same packaging campaign as the recalled lot
Published: June 18, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 11, 2015Historical recordClass II

CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-013-15.

by Carefusion 2200 Inc

Reason: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner. The available iodine in the product is less than as stated on the product label.
Published: June 11, 2014
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 11, 2015Historical recordClass II

CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-003-18

by Carefusion 2200 Inc

Reason: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner. The available iodine in the product is less than as stated on the product label.
Published: June 11, 2014
Distribution: Nationwide

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Data last updated: November 11, 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.