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Recall totals

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

37,066

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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 Terminated Historical recordClass II

Alprazolam Tablets, USP, 2 mg, CIV, packaged in: a)100-count bottle (NDC 51991-0707-01) and b) 500-count bottle (NDC 51991-0707-05), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01), b) 500-count bottle (NDC 51991-0706-05) and c) 1,000-count bottle (NDC 51991-0706-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01), b) 500-count bottle and c) 1,000-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product: Pingo Peanut Butter Cookie Hot Chocolate packaged in single…
Reason: Coffee pods may contain undeclared peanut residue
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product: Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single…
Reason: Coffee pods may contain undeclared peanut residue
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mead Johnson & Company

Product: ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
Reason: Reckitt, a producer of nutrition products, announced today that out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii.
Published: March 22, 2023
Distribution: AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI,…

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.…
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.)…
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product: Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection p…
Reason: Coffee pods may contain undeclared peanut residue
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Purely Soothing MSM Nasal Spray, 15%, packaged in 30ml, 1.014 fl. oz bottles, Manufactured by: Pharmedica USA, Phoenix, AZ, UPC 7 31034 91380 5

by Pharmedica USA, LLC

Reason: CGMP Deviations
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.

by Pharmedica USA, LLC

Reason: Non-Sterility
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.

by Nanomaterials Discovery Corporation

Reason: Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

by Akron Pharma, Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%), packaged in 1 oz. (28.3g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756

by Ecometics, Inc.

Reason: CGMP DEVIATIONS
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz, liquid oral rinse plastic bottles, Manufactured for: All USA Direct LLC, Broadview, IL 60155

by Ecometics, Inc.

Reason: CGMP DEVIATIONS
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nose Better Gel (0.75% Camphor, 0.50% Menthol, 0.50% Allantoin), packaged in 0.46 oz. (13g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756

by Ecometics, Inc.

Reason: CGMP DEVIATIONS
Published: March 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Soltice Quick-RUB (Menthol 5.1%, Camphor 5.1%) packaged in a) 1.33 oz (37g) plastic jars and b) 3 Oz (85g) plastic jars

by Ecometics, Inc.

Reason: CGMP DEVIATIONS
Published: March 15, 2023
Distribution: Nationwide

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Data last updated: September 12, 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.