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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 September 28, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Poppie International INC

Product: Poppies Belgian Eclairs,Net Wt. 710 g/25 oz., Contents 50 ct…
Reason: Product contains milk product from a supplier that is recalling product due to the possible presence of Salmonella.
Published: January 25, 2017
Distribution: AZ, CA, CO, FL, HI, IA, ID, IL, KS, MN,…

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FDA Recall United States Terminated Historical recordClass I

Poppie International INC

Product: Delizza Patisserie, Beligian Mini Chocolate Dipped Cream Puf…
Reason: Product contains milk product from a supplier that is recalling product due to the possible presence of Salmonella.
Published: January 25, 2017
Distribution: AZ, CA, CO, FL, HI, IA, ID, IL, KS, MN,…

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FDA Recall United States Terminated Historical recordClass I

Poppie International INC

Product: Delizza Patisserie, Belgian Custard Cream Mini Eclairs, Net…
Reason: Product contains milk product from a supplier that is recalling product due to the possible presence of Salmonella.
Published: January 25, 2017
Distribution: AZ, CA, CO, FL, HI, IA, ID, IL, KS, MN,…

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FDA Recall United States Terminated Historical recordClass II

Chesapeake Spice Company, LLC

Product: ENCHILADA SEASONING NET WEIGHT: 50. 00 LBS
Reason: Milk Ingredient that was recalled went into Chesapeake Spice products.
Published: January 25, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Chesapeake Spice Company, LLC

Product: GREEN BEAN SAUCE SEASONING NET WEIGHT: 50.00 LBS
Reason: Milk Ingredient that was recalled went into Chesapeake Spice products.
Published: January 25, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Herr Foods, Inc.

Product: Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.…
Reason: Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient . The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Herr Foods, Inc.

Product: Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 o…
Reason: Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.625 oz., and 8.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient. The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 30 mg over 9 hours (3.3 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5555-3.

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 20 mg over 9 hours (2.2 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5554-3.

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 10 mg over 9 hours (1.1mg/hr), packaged in- 30 count per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc, Miami, FL 33186, NDC 68968-5552-3

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1723-20

by Pharm D Solutions, LLC

Reason: Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct
Published: January 18, 2017
Distribution: AZ and WA

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FDA Recall Terminated Historical recordClass III

Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1709-04

by Pharm D Solutions, LLC

Reason: Incorrect/Undeclared Excipient; product description section of testosterone cypionate incorrectly states "in grapeseed oil" instead of "in sesame oil" . The primary panel is correct
Published: January 18, 2017
Distribution: AZ and WA

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FDA Recall Terminated Historical recordClass III

Cytotec (misoprostol) Tablets, 200 mcg, 100 Tablets blister pack (10X10), For in-institution use only, Rx only, Distributed by G.D. Searle, Division of Pfizer, Inc., NY, NY --- NDC 0025-1461-34

by Pfizer Inc.

Reason: Failed Impurities/Degradations Specifications; Out of specification results for two known degradation products and total impurities at 18 months
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Williams-Sonoma

Product: Williams-Sonoma Meyer Lemon Poppy Quick bread mix, NET WT. 1…
Reason: Williams Sonoma was notified by their contract manufacturer that high heat non fat dry milk powder that is now under recall for Salmonella was used in production of one of their quick bread mixes.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product: Cardboard sleeve: Cheese Club express mac Macaroni & Cheese…
Reason: Fourth Street Barbecue Inc./ Packing Division has initiated the voluntary recall of Cheese Club Express Mac & Cheese 4 cup dinner and Double Takes Macaroni & Cheese 2 cup dinner due to possible health risk. The powdered cheese packets may be impacted by milk powder ingredients recalled by Valley Milk Products, LLC contaminated with Salmonella.
Published: January 18, 2017
Distribution: CA CT GA IL MS OK PA SC VA WA

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FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product: Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Dis…
Reason: Fourth Street Barbecue Inc./ Packing Division has initiated the voluntary recall of Cheese Club Express Mac & Cheese 4 cup dinner and Double Takes Macaroni & Cheese 2 cup dinner due to possible health risk. The powdered cheese packets may be impacted by milk powder ingredients recalled by Valley Milk Products, LLC contaminated with Salmonella.
Published: January 18, 2017
Distribution: CA CT GA IL MS OK PA SC VA WA

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FDA Recall United States Terminated Historical recordClass II

Brand Castle LLC

Product: In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box,…
Reason: The firm was notified by one of their ingredient suppliers that their facility and finished product test positive for Salmonella.
Published: January 18, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product: Super Nacho (No-Pho, Gluten Free). Product Code: T4034. 50 l…
Reason: Products have been recalled due to potential for Salmonella contamination.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product: Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags
Reason: Products have been recalled due to potential for Salmonella contamination.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product: Triple Cheese Blend - No Color. Product Code: T4008. 50 lb b…
Reason: Products have been recalled due to potential for Salmonella contamination.
Published: January 18, 2017
Distribution: Nationwide

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Data last updated: September 28, 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.