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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 19, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: Milk Chocolate Wafer, Item # 51407 (R&D Sample).
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: Milk Chocolate Flavored Confectionery Coating Bulk (MB), Ite…
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: Milk Chocolate Crunch Bulk OTBD, Item # 56546.
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: 1057556 Milk Chocolate Flavored IC Coating, Item # 56546. Bu…
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: NGMO White Confectionery Wafer, Item # 60975. Net Wt. 25 lbs…
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: White Chocolate Wafer, Item # 59152. Net Wt. 50 lbs (22.68kg…
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass III

Clasen Quality Chocolate Inc.

Product: Milk Chocolate Flavored Confectionery Coating (MB), Item #:…
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: Snow White Chocolate, Item #: 60949. Bulk tanker.
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass II

Clasen Quality Chocolate Inc.

Product: 1085343 10M Milk Chocolate Flavored Confectionery Drop (MB),…
Reason: Potential Salmonella contamination.
Published: June 26, 2024
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass I

Docetaxel Injection, USP, 160 mg per 16 mL (10 mg per mL), 1 x 16 mL Multi-Dose Vial, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-254-08

by Sagent Pharmaceuticals

Reason: Presence of Particulate Matter: Presence of particulate matter from the stopper in the drug product.
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Docetaxel Injection, USP, 80 mg per 8 mL (10 mg per mL), 1 x 8 mL Multi-Dose Vial, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-254-08

by Sagent Pharmaceuticals

Reason: Presence of Particulate Matter: Presence of particulate matter from the stopper in the drug product.
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 30 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-0114-04

by Organon Llc

Reason: Defective Container
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 14 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-114-03

by Organon Llc

Reason: Defective Container
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 60 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-114-02

by Organon Llc

Reason: Defective Container
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension, 1%, 0.5%, 0.075%, 5mL, Quantity: 20mL, Rx Only, Compounded by: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ NDC 71384-310-05

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1% 5.5mL, Rx Only, This is a compounded drug. NOT FOR RESALE. OFFICE USE ONLY Compounded by: Imprimis NJOF, LLC., 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852 NDC: 71384-514-05

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for: Pacira Pharmaceuticals Inc., San Diego, CA 92121, NDC 65250-001-01. Diluent Vial Label: Diluent, 5mL, Sterile single use, Rx only, Manufactured for Pacira Pharmaceuticals Inc., NDC 65250-002-01. Carton Label: Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for: Pacira Pharmaceuticals Inc., San Diego, CA 92121, NDC 65250-003-01.

by PACIRA PHARMACEUTICALS INC

Reason: Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6 weeks at 25 degrees C.
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Phenazopyridine HCl Tablets USP, 100 mg, 100-count bottles, Rx Only, Manufactured by: Winder Laboratories, LLC. 716 Patrick Industrial Lane, Winder, GA 30680, NDC 75826-114-10,

by Winder Laboratories, LLC

Reason: Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
Published: June 19, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 26, 2025Historical recordClass I

GRANDE CHEESE COMPANY

Product: Grande Grande Primo Y45 Cultured Dairy Product. Product Cod…
Reason: Possible Salmonella contamination.
Published: June 19, 2024
Distribution: AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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FDA Recall United States TerminatedTerminated: June 26, 2025Historical recordClass I

GRANDE CHEESE COMPANY

Product: Grande Ultra 9150 Whey Protein Isolate. Product Code: 3232…
Reason: Possible Salmonella contamination.
Published: June 19, 2024
Distribution: AR, CA, CO, GA, ID, IL, IN, KS, KY, LA,…

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Data last updated: October 19, 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.