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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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 September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Fajita Mix, 6-oz. packaged in a clamshell
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Tri-Pepper Dice, 6-oz. packaged in a clamshell and Dice Tri-…
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Creole Mix, 6-oz. packaged in a clamshell
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Green Pepper Diced, 6-oz. packaged in a clamshell
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product: Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g…
Reason: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Vegetable Kabob, 23-oz. packaged in an overwrap; Kabob Sensa…
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Stir Fry Vegetable, 10-oz. packaged in an overwrap
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Products, LLC

Product: Fajita Blend, 12-oz. packaged in an overwrap
Reason: Potential contamination with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Alabama, Florida, Georgia, Louisiana, an…

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FDA Recall United States Terminated Historical recordClass II

Rajbhog Distributors GA Inc

Product: Rajbhog Sweet, JALEBI, Net Weight 11.2 oz. (315 grams), Dist…
Reason: Undeclared Allergen, Almond.
Published: October 4, 2017
Distribution: AL, FL, GA, MS, NC, SC and TN.

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FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product: LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
Reason: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product: FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283…
Reason: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published: October 4, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass I

Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water for Injection USP and one transfer device. Manufactured by: Genentech, Inc. 1 DNA Way, South San Francisco, CA 84080-4990. NDC: 50242-0085-27

by Genentech, Inc.

Reason: Non-Sterility:presence of cracked or chipped glass at the neck of Sterile Water for Injection vials.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient, packaged in a) 100 g jar (NDC 38779-0989-05, b) 1 kg jar (NDC 38779-0989-09), and 25 kg drum (NDC 38779-0989-07), Rx only, Packed by Medisca Inc., Plattsburgh, NY 12901, CAS: 60-32-1. 38779-0989-05; jar, 300 ml, white HDPE 38779-0989-07; drum, 15 gallon, Fiber 38779-0989-09; 2.8L, white, HDPE

by Medisca, Inc.

Reason: CGMP Deviations: Product manufactured for Industrial Use but was labeled and distributed for Pharmacy Compounding Use.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Procrit (epoetin alfa), 10,000 units/mL, packaged in a) box of 6 single use 1 mL vials (NDC 59676-310-01), b) box of 25 single use 1 mL vials (NDC 59676-310-02), Rx Only, Manufactured by: Amgen, Inc. Thousand Oaks, CA 91320, Manufactured for: Janssen Products, LP Horsham, PA 19044

by Amgen, Inc.

Reason: Presence of particulate matter: glass flakes identified as lamellae observed during a routine quality inspection.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours (1.6 mg/hr) Rx Only Contains: 30 Patches Manufactured for: Noven Therapeutics, LLC. Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC# 68968-5553-3

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Products no longer meet the release liner removal specification and/or z-statistic.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) Rx Only Contains: 30 Patches Manufactured for: 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: Products no longer meet the release liner removal specification and/or z-statistic.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) Rx Only Contains: 30 Patches Manufactured for: 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: Products no longer meet the release liner removal specification and/or z-statistic.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Rx Only Contains: 30 Patches Manufactured for: 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: Products no longer meet the release liner removal specification and/or z-statistic.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levophed (norepinephrine bitartrate) injection, USP, 4 mg/4 mL (1mg/mL), 4mL Fill in 5 mL Single dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3375-04

by Pfizer Inc.

Reason: Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.
Published: September 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl Injection, USP, 2 mg/mL, 1mL Single-use vial, packaged in cartons of 25 vials, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3365-11 (carton) and 0409-3365-01(vial)

by Pfizer Inc.

Reason: Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.
Published: September 27, 2017
Distribution: Nationwide

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Data last updated: September 30, 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.