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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: WA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 17, 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 OngoingHistorical recordClass II

BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, Applicator is sterile if package is intact, Flammable, External Use Only, 1 mL Applicator per pouch, 60 Applicators per inner carton, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., Made in the USA, Catalog Number 930480, NDC 54365-400-31.

by CareFusion 213, LLC

Reason: Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.
Published: May 28, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Medium Salsa Costco item, is refrigerated product and packag…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Verde Salsa is refrigerated product, packaged in Polypropyle…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Mens Room Roasted Red Salsa is refrigerated product, package…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Pineapple Mango Salsa is refrigerated product, packaged in…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Traditional Salsa is refrigerated product, packaged in Polyp…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Hot Salsa is refrigerated product, packaged in Polypropylene…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Medium Salsa is refrigerated product, packaged in Polypropyl…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Frobright Salsary, LLC

Product: Mild Salsa is refrigerated product, packaged in Polypropylen…
Reason: Salsa products are recalled due to potential contamination with wood particles.
Published: May 28, 2025
Distribution: Distributed in AK, ID, OR, and WA.

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FDA Recall United States TerminatedTerminated: July 8, 2025Historical recordClass I

My Life Inc

Product: Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg…
Reason: Undeclared milk allergen
Published: May 28, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.

by Empower Clinic Services, LLC dba Empower Pharmacy

Reason: Lack of Assurance of Sterility
Published: May 21, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube per Carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France.

by L'Oreal USA

Reason: cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
Published: May 21, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatment 0.7 fl. oz. (20 mL: UPC 883140035275) Tube, (benzoyl peroxide 0.5% and benzoyl peroxide 5.5% and salicylic acid 2%), La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France, UPC 883140035282 (kit).

by L'Oreal USA

Reason: cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
Published: May 21, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-Posay, France, UPC 883140500759.

by L'Oreal USA

Reason: Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.
Published: May 21, 2025
Distribution: Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Bondsforever, Inc dba Shastha Foods

Product: Dixit Foods, Pohe, Net Wt. 110 g, Ingredients: Rice Flakes,…
Reason: Undeclared allergens (milk and/or peanuts).
Published: May 21, 2025
Distribution: Multiple states

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FDA Recall United States OngoingHistorical recordClass II

Bondsforever, Inc dba Shastha Foods

Product: Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients:…
Reason: Undeclared allergens (milk and/or peanuts).
Published: May 21, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0121-01

by BSO LLC

Reason: Presence of Particulate Matter: Glass particles were found in pellet vials.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0122-01

by BSO LLC

Reason: Presence of Particulate Matter: Glass particles were found in pellet vials.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0124-01

by BSO LLC

Reason: Presence of Particulate Matter: Glass particles were found in pellet vials.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0125-01

by BSO LLC

Reason: Presence of Particulate Matter: Glass particles were found in pellet vials.
Published: May 14, 2025
Distribution: Nationwide

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Data last updated: October 17, 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.