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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: NE ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 7, 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 United States TerminatedTerminated: January 14, 2020Historical recordClass I

WHOLE FOODS MARKET

Product: Caulilini, Roasted Grape & Curry Vinaigrette Cindy's served…
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass I

WHOLE FOODS MARKET

Product: Salad Bar, Trend Alert Pickled Pear & Brussels Sprouts serv…
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass I

WHOLE FOODS MARKET

Product: Salad Bar, Brussels Sprouts Shredded served on the salad bar
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass II

WHOLE FOODS MARKET

Product: Caulilini, Roasted with Roasted Garlic served on the salad b…
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass I

WHOLE FOODS MARKET

Product: Caulilini & Broccoli Lemon Caper served on the salad bar
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass II

WHOLE FOODS MARKET

Product: Wedge Greek Salad served on the salad bar
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass I

WHOLE FOODS MARKET

Product: Vegetable Power Blend served on the salad bar
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 14, 2020Historical recordClass II

WHOLE FOODS MARKET

Product: Trend Alert Caulilini with Vadouvan Curry served on the sala…
Reason: Possible contamination with Listeria monocytogenes
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 3, 2020Historical recordClass II

Gold Standard Baking, Inc.

Product: Freshness Guaranteed Croissants in clear plastic 12oz clamsh…
Reason: Product is missing ingredient and nutrition label on bottom of clamshell retail package. Missing ingredients include allergens MILK, WHEAT, and SOY
Published: December 25, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 21, 2024Historical recordClass I

Mirtazapine Tablets, USP, 7.5 mg, 500-count tablets, Rx only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810 NDC 13107-001-05

by AuroMedics Pharma LLC

Reason: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg tablets, 500-count bottles, contain 500-count bottles of Mirtazapine 15mg tablets labelled as Mirtazapine 7.5 mg tablets.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 21, 2024Historical recordClass I

Mirtazapine Tablets, USP, 15 mg, 500-count tablets, Rx only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810 NDC 13107-031-05

by AuroMedics Pharma LLC

Reason: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg tablets, 500-count bottles, contain 500-count bottles of Mirtazapine 15mg tablets labelled as Mirtazapine 7.5 mg tablets.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 27, 2021Historical recordClass II

Petroleum jelly (White Petrolatum) USP 100%, packaged in a) 1 oz tube (UPC 1182298884), b) 2.5 oz tube (UPC 1182298541), Distributed by Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011

by OraLabs, Incorporated

Reason: Cross contamination with other products: undeclared contaminants of phenol and camphor in petroleum jelly tubes.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 7, 2020Historical recordClass II

Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC 70004-0723-09

by SCA Pharmaceuticals, LLC

Reason: Presence of Foreign Substance: Foreign material found inside the vial (manufacturer).
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 15, 2024Historical recordClass III

Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited Plot No. B-25, MIDC, Shendra Aurangabad, Maharashtra -431210, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective delivery system; product is not foaming or is coming out as liquid.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 15, 2024Historical recordClass III

Clobetasol Propionate Foam, 0.05%, a) 50 g pack (NDC 68462-608-27) and b) 100 g pack (NDC 68462-608-94), Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot No.: B-25, MIDC, Shendra Aurangabad - 431210, Maharashtra, India Manufactured for: Glenmark Pharmaceuticas Inc. USA Mahwah, NJ 07430

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective delivery system; product is not foaming or is coming out as liquid.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 1, 2020Historical recordClass II

Hydromorphone HCL and Clonidine HCL and Fentanyl Citrate in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.

by Coast Quality Pharmacy, LLC dba Anazao Health

Reason: Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 1, 2020Historical recordClass II

Hydromorphone HCL and Bupivacaine HCL and Baclofen and Clonidine HCL in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.

by Coast Quality Pharmacy, LLC dba Anazao Health

Reason: Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 1, 2020Historical recordClass II

Hydromorphone HCL and Bupivacaine HCL and Baclofen and Clonidine HCL and Fentanyl Citrate in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.

by Coast Quality Pharmacy, LLC dba Anazao Health

Reason: Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 1, 2020Historical recordClass II

Fentanyl Citrate and Clonidine HCL and Morphine Sulfate and Baclofen in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.

by Coast Quality Pharmacy, LLC dba Anazao Health

Reason: Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Published: December 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 1, 2020Historical recordClass II

Fentanyl Citrate and Bupivacaine HCL and Clonidine HCL in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.

by Coast Quality Pharmacy, LLC dba Anazao Health

Reason: Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Published: December 18, 2019
Distribution: Nationwide

View recall →

Data last updated: November 7, 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.