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Recall totals

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

37,061

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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 10, 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

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

FDA Recall United States Terminated Historical recordClass III

Preventics, Inc. dba Legere Pharmaceuticals

Product: Probese Caps, dietary supplement with Iron. 90-count bottle…
Reason: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Preventics, Inc. dba Legere Pharmaceuticals

Product: Super ProTHIN Plus, dietary supplement. Seven Packets with…
Reason: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Preventics, Inc. dba Legere Pharmaceuticals

Product: Prothin, dietary supplement. Seven Packets containing 2 tab…
Reason: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134

by Umary-USA.com

Reason: Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone and Diclofenac.
Published: June 25, 2025
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295

by Umary-USA.com

Reason: Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone, Diclofenac and Omeprazole.
Published: June 25, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Gentamicin Injection, USP, (PEDIATRIC), 20 mg per 2 mL (10 mg per mL*), 2 mL Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ, 08520 Vial- NDC 55150-401-01, Carton NDC 55150-401-25

by Eugia US LLC

Reason: Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis.
Published: June 25, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N., Seattle, WA 98109, NDC 72288-405-10

by Aurobindo Pharma USA Inc

Reason: cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets).
Published: June 25, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass I

GBC Food Services, LLC

Product: Cucumber Carrot Ranch Pack 20oz 850065403557 Purchase Dates:…
Reason: Potential to be contaminated with Salmonella
Published: June 25, 2025
Distribution: IN, IL, OH, KY, TN, MS, MO, AR and, MI.

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FDA Recall United States Ongoing Historical recordClass I

GBC Food Services, LLC

Product: Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2…
Reason: Potential to be contaminated with Salmonella
Published: June 25, 2025
Distribution: IN, IL, OH, KY, TN, MS, MO, AR and, MI.

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FDA Recall United States Ongoing Historical recordClass I

GBC Food Services, LLC

Product: Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to 0…
Reason: Potential to be contaminated with Salmonella
Published: June 25, 2025
Distribution: IN, IL, OH, KY, TN, MS, MO, AR and, MI.

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FDA Recall United States Ongoing Historical recordClass I

GBC Food Services, LLC

Product: Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/20…
Reason: Potential to be contaminated with Salmonella
Published: June 25, 2025
Distribution: IN, IL, OH, KY, TN, MS, MO, AR and, MI.

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FDA Recall United States Ongoing Historical recordClass I

GBC Food Services, LLC

Product: Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purcha…
Reason: Potential to be contaminated with Salmonella
Published: June 25, 2025
Distribution: IN, IL, OH, KY, TN, MS, MO, AR and, MI.

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FDA Recall Ongoing Historical recordClass II

Icosapent Ethyl Capsules 1 gram, 120 Capsules per Bottle, Rx Only, Manufactured by Doppel Farmaceutici s.r.l., Piacenza, Italy, Distributed by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1592-7.

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Tablet/Capsule specifications; a product complaint was reported for burnt or melted capsules. This was determined to be a result of oxidation by leakage of capsule contents.
Published: June 18, 2025
Distribution: IL, PA, & MS

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FDA Recall Ongoing Historical recordClass I

Sulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg, Rx Only, a) 100 Tablets per Bottle, NDC: 65162-271-10, b) 500 Tablets per Bottle, NDC: 65162-271-50, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad, 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807.

by Amneal Pharmaceuticals, LLC

Reason: Microbial contamination of non-sterile products: tablets may exhibit black spots due to microbial contamination.
Published: June 18, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Levothyroxine Sodium Tablets, USP 112 mcg (0.112mg), 1000 tablets, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540. Manufactured by: Macleods Pharmaceuticals Ltd. Sarigam, Valsad, Gujarat, India, NDC 33342-398-44.

by Macleods Pharmaceuticals Ltd

Reason: Presence of a foreign substance: black hair found embedded in tablet.
Published: June 18, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 200 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascent Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-544-68

by Ascend Laboratories, LLC

Reason: Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
Published: June 18, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 100 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascent Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-544-88

by Ascend Laboratories, LLC

Reason: Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
Published: June 18, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.

by SAINI TRADE INC

Reason: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published: June 18, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.

by SAINI TRADE INC

Reason: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published: June 18, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.

by SAINI TRADE INC

Reason: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
Published: June 18, 2025
Distribution: Nationwide

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Data last updated: September 10, 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.