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Recall totals

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

37,116

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potatoPublished September 16, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 18, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v), Packaged as a) 2 fl oz / 60 ml bottle, UPC 8 14266 02371 6 b) 7.5 fl oz / 221 ml bottle, UPC 8 14266 02362 4 c) 15.2 fl oz (450 ml) bottle, UPC 8 14266 02392 1, d) 17 fl oz / 503 ml bottle with blue cap or pump bottle, UPC 8 14266 02409 6, e) 18 fl oz / 532 ml bottle, UPC 8 14266 02391 4, f) 33.8 fl oz / 1 L straight or curved bottle, UPC 8 14266 02369 3 g) 70 fl oz / 2.07L bottle, UPC 8 14266 02367 9 h) 1.05 GAL / 4L bottle, UPC 8 14266 02368 6; Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, San Antonio, Texas, 78257, Made in Mexico.

by 4e Brands North America, Llc

Reason: CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4 b) 7.5 fl. oz./221 ml bottle, UPC 8 14266 02362 4 b) 33.8 fl. oz./1L bottle, UPC 8 14266 02369 3, Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, San Antonio, Texas, 78257, Made in Mexico.

by 4e Brands North America, Llc

Reason: CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% Natural Boost with Tea Tree Oil, (70% ethyl alcohol), Packaged as a) 18 fl oz / 532 ml bottle, UPC 8 14266 02408 9 b) 33.8 fl oz / 1L bottle, UPC 8 14266 02374 7, Distributed in USA and Canada BY: 4e Brands Northamerica LLC. 17806 IH-10W, Suite 300, San Antonio, Texas, 78257. Made in Mexico.

by 4e Brands North America, Llc

Reason: CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Buprenorphine Transdermal System 5 mcg/hour, 4 transdermal systems/4 disposal units per carton, Rx Only, Manufactured by: 3M Drug Delivery Systems, 19901 Nordhoff street, Northridge, CA 91324 USA, Manufactured for: Teva Pharmaceuticals USA Inc., North Wales, PA 19454, carton NDC: 0093-3656-40, patch NDC: 0093-3656-21.

by Teva Pharmaceuticals USA

Reason: Failed Stability Specifications: Below specification result for buprenorphine release rate.
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

RIOMET ER (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL 16 oz. For Oral Use Only Rx Only Manufactured by: Sun Pharmaceuticals Industries Limited Mohali, India Distributed by: Sun Pharmaceuticals Industries, Inc. Cranbury, NJ 08512 NDC 10631-019-17

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: CGMP Deviations: Detection of N-nitrosodimethylamine (NDMA) impurity in finished drug product.
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Strides Pharma Inc.Potassium Chloride Extended-Release Tablets, USP 8mEq (600 mg) 100 Tablets Rx Only Manufactured by: Strides Pharma Science Limited Bengaluru -562106 India Distributed by: Strides Pharma Inc., East Brunswick NJ 08816 NDC 64380-860-06

by Strides Inc.

Reason: Failed Dissolution Specifications
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product: Nice! Organic White Cheddar Popcorn, 4.5 oz. bag, UPC 049022…
Reason: Foreign material, pieces of glass may be in the product
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product: Nature's Promise Organic Lightly Salted Popcorn, 6 oz. bag,…
Reason: Foreign material, pieces of glass may be in the product
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product: Cretors Organic Extra Virgin Olive Oil Popcorn, 4.4 oz. bag,…
Reason: Foreign material, pieces of glass may be in the product
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product: 365 Everyday Value Organic Classic Salted Popcorn, 6 oz. bag…
Reason: Foreign material, pieces of glass may be in the product
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product: 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn,…
Reason: Foreign material, pieces of glass may be in the product
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product: 365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz.…
Reason: Foreign material, pieces of glass may be in the product
Published: October 7, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Dianne's Fine Desserts

Product: Devonshire Bake Shop brand Lemon Italian Cream Cake, 10 , Ye…
Reason: Product contains undeclared peanuts.
Published: October 7, 2020
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass I

Red-E Tablet, Proprietary Blend 3000 mg**, packaged in 1-count plastic bag stapled with cardboard labeling.

by The Protein Shoppe

Reason: Marketed Without An Approved NDA/ANDA: product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug fro which the safety and efficacy have not been established and therefore subject to recall.
Published: September 30, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma Solutions, 160 N Pharma Drive, Morrisville, NC 27560, Distributed by: Perrigo, Allegan, MI 49010 NDC 45802-088-01

by Perrigo Company PLC

Reason: Defective Delivery System: Sustained trend of failure to dispense complaints.
Published: September 30, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Gilster-Mary Lee Corp.

Product: Cadia Organic Unsalted Microwave Popcorn, Net Wt. 8.4 oz (2…
Reason: Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published: September 30, 2020
Distribution: Distributed to grocery stores in the fol…

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FDA Recall United States Terminated Historical recordClass II

Gilster-Mary Lee Corp.

Product: Microwave popcorn packaged in the following ways: 1) Full…
Reason: Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published: September 30, 2020
Distribution: Distributed to grocery stores in the fol…

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FDA Recall United States Terminated Historical recordClass II

Gilster-Mary Lee Corp.

Product: Buttered microwave popcorn packaged in the following ways:…
Reason: Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published: September 30, 2020
Distribution: Distributed to grocery stores in the fol…

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FDA Recall United States Terminated Historical recordClass II

Gilster-Mary Lee Corp.

Product: Light microwave popcorn packaged in the following ways: 1…
Reason: Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published: September 30, 2020
Distribution: Distributed to grocery stores in the fol…

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FDA Recall United States Terminated Historical recordClass II

Gilster-Mary Lee Corp.

Product: Lightly salted microwave popcorn packaged in the following w…
Reason: Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published: September 30, 2020
Distribution: Distributed to grocery stores in the fol…

View recall →

Data last updated: September 18, 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.