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Recall totals

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

37,204

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/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

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).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass I

SLIM TRIM U Capsules, 250mg, 60-count bottles, Manufactured for Floyd Nutrition

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

SlimeX-15 Capsules, 15 mg, 30-count bottles, Marketed by: Signature Pharmaceuticals Ltd. MUMBAI-400-030 Manufactured in India by: HAB Pharmaceuticals & Research Limited 10-Pharma City, SIDCUL, Selaqui, Dehradun, 248 197

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St. #392 Columbus, IN 47203

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Oasis Capsules, 500mg, 45-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando FL 32801 (407)930-4043

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

La' Trim Plus Capsules, 350 mg, 60-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando, FL 32801 (407) 930-4043

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Jenesis Capsules, 350 mg, 60-count bottles, Manufactured for Timeless Solutions 1810 E. Sahara Ave #100 Las Vegas, Nevada 89104

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Infinity Capsules, 500 mg, 30-count bottle, Manufactured for Floyd Nutrition

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

EVOLVE BEE POLLEN Capsules, 250mg, 60-count bottles, Manufactured for 2637 E. Atlantic Blvd, Pompano Beach, Florida, 33062 WWW.BEEEXTREMELYAMAZED.COM

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Asset extreme+PLUS Capsules, 500 mg, 30-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com www.allnaturalbeelievers.com

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Asset BOLD Capsules, 500 mg, 60-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com

by Bee Extremely Amazed LLC

Reason: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

by Hospira Inc.

Reason: Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.
Published: July 13, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

All Malarone (atovaquone and proguanil) Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All baclofen Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All diethylstilbestrol Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All e2-e3-p4 Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All tacrolimus Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All Nitro Paste (nitroglycerin) Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All hydroquinone Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All clobetasol Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

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FDA Recall Terminated Historical recordClass II

All methyltestosterone Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.

by Reliable Rexall-A Compounding Pharmacy

Reason: Lack of Processing Controls
Published: July 13, 2016
Distribution: U.S. Including: CA, HI, NM

View recall →

Data last updated: September 30, 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.