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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: May 1, 2019Historical recordClass II

Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-401-02.

by Ingenus Pharmaceuticals Llc

Reason: Superpotent Drug: High out of specification assay value results for potency.
Published: July 11, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 1, 2019Historical recordClass II

Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-402-05.

by Ingenus Pharmaceuticals Llc

Reason: Superpotent Drug: High out of specification assay value results for potency.
Published: July 11, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 4, 2018Historical recordClass II

Icelandic Provisions Inc.

Product: Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC:…
Reason: Cups containing coconut skyr yogurt may have been mislabeled as vanilla skyr yogurt.
Published: July 11, 2018
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 10, 2018Historical recordClass I

Utz Quality Food Inc

Product: Good Health Organic Tortillas; Black Bean & Rice; Net Wt 5.5…
Reason: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
Published: July 4, 2018
Distribution: AL AL AR AZ CT DC DE FL GA IL…

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FDA Recall United States TerminatedTerminated: September 10, 2018Historical recordClass I

Utz Quality Food Inc

Product: Golden Flake TORTIYAHS! Superior Dipping Chips; Net Wt 12.5…
Reason: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
Published: July 4, 2018
Distribution: AL AL AR AZ CT DC DE FL GA IL…

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FDA Recall United States TerminatedTerminated: September 10, 2018Historical recordClass I

Utz Quality Food Inc

Product: Weis Signature Collection No Salt Added White Corn Tortilla…
Reason: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
Published: July 4, 2018
Distribution: AL AL AR AZ CT DC DE FL GA IL…

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FDA Recall United States TerminatedTerminated: September 10, 2018Historical recordClass I

Utz Quality Food Inc

Product: Utz Organic Yellow Corn Tortillas, Net Wt 9 oz; UTZ Quality…
Reason: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
Published: July 4, 2018
Distribution: AL AL AR AZ CT DC DE FL GA IL…

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FDA Recall United States TerminatedTerminated: September 10, 2018Historical recordClass I

Utz Quality Food Inc

Product: Utz Organic Blue Corn Tortillas; Net Wt 9 oz; UTZ Quality Fo…
Reason: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
Published: July 4, 2018
Distribution: AL AL AR AZ CT DC DE FL GA IL…

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FDA Recall United States OngoingHistorical recordClass III

Absonutrix

Product: Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bott…
Reason: The firm was informed that the product did not contain vitamin B12 (Methylcobalamyn) as listed on the label.
Published: July 4, 2018
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: September 10, 2018Historical recordClass I

Utz Quality Food Inc

Product: Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Cor…
Reason: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
Published: July 4, 2018
Distribution: AL AL AR AZ CT DC DE FL GA IL…

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FDA Recall TerminatedTerminated: November 8, 2019Historical recordClass III

Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC 55111-123-05), Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 8, 2019Historical recordClass III

Atorvastatin Calcium Tablets, 20 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-122-90

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 8, 2019Historical recordClass III

Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-121-90

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

5% Dextrose Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7922-02

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

0.9% Sodium Chloride Injection, USP, 100 mL bag, Rx Only ,Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7984-37

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

0.9% Sodium Chloride Injection, USP, 100 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7984-23

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

0.9% Sodium Chloride Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7983-02

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

0.45% Sodium Chloride Injection, USP, 100 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7730-37

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 14, 2020Historical recordClass II

Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-124-90 UPC 355111124900

by Dr. Reddy's Laboratories, Inc.

Reason: Presence of Foreign Substance: A product complaint was received for a defective tablet with an embedded foreign object observed in a bottle.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 18, 2018Historical recordClass I

Kellogg Company

Product: Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
Reason: Kellogg North America initiated a voluntary recall of Kellogg s Honey Smacks, 15.3 oz. and 23 oz., due to potential contamination with Salmonella.
Published: June 27, 2018
Distribution: Domestic: Alabama Arizona Arkansas Ca…

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Data last updated: November 8, 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.