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Recall totals

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

37,113

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 15, 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

Micafungin for Injection, 50 mg/vial, Single-Dose Vial, Sterile, Rx Only, For Intravenous Infusion Only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089. NDC 70594-036-01

by XELLIA PHARMACEUTICALS USA, LLC

Reason: Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.
Published: September 1, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CAHILLS FARM CHEESE LIMITED

Product: Lidl Preferred Selection-Red Wine Cheddar - 7 oz.
Reason: Cheese may be contaminated with Listeria monocytogenes.
Published: September 1, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CAHILLS FARM CHEESE LIMITED

Product: Lidl Preferred Selection-Irish Stout Cheddar - 7 oz.
Reason: Cheese may be contaminated with Listeria monocytogenes.
Published: September 1, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CAHILLS FARM CHEESE LIMITED

Product: Cahills Ireland Red Wine - 5 lbs. Waxed Deli Wheel
Reason: Cheese may be contaminated with Listeria monocytogenes.
Published: September 1, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CAHILLS FARM CHEESE LIMITED

Product: 1. Cahills Ireland Original Irish Porter 5lbs.Waxed Deli Whe…
Reason: Cheese may be contaminated with Listeria monocytogenes.
Published: September 1, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CAHILLS FARM CHEESE LIMITED

Product: Cahills Ireland Whiskey Cheese - 5lb. Waxed Deli Wheel
Reason: Cheese may be contaminated with Listeria monocytogenes.
Published: September 1, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Carvedilol Tablets, USP 25 mg, 500 Tablets bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 0853, NDC 68382-095-05

by Zydus Pharmaceuticals (USA) Inc

Reason: Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were found in the bottle
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Triamcinolone Acetonide Ointment USP, 0.1% 80 g cartons, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-014-80 ; packaged in tubes.

by Teligent Pharma, Inc.

Reason: Correct Labeled Product Mispack
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Econazole Nitrate Cream 1%, 85 grams bulk shippers, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-022-85 ; packaged in tubes.

by Teligent Pharma, Inc.

Reason: Correct Labeled Product Mispack
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laboratories limited, Srikakulam District, 532 409 INDIA, NDC 55111-180-15.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Tablet/Capsule Specification: Some tablets are shaved
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Adenosine Injection, USP, 60mg/20 mL (3 mg/mL), 20 mL single-dose vial, Rx only, Mfd in the USA for: NorthStar Rx LLC Memphis, TN 38141, NDC 16714-180-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Leucovorin Calcium for Injection, USP 350 mg/vial, 17.5 mL single-use vials, Rx only, Manufactured by: Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0703-5145-91

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Leucovorin Calcium for Injection, USP 100 mg/vial, 10 mL single-use vials, Rx only, Teva Parenteral Medicines, Inc. Irvine, CA 92618, NDC 0703-5140-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Octreotide Acetate Injection 50 mcg/mL, 1 mL single-dose vial, Rx only, Teva Pharmaceuticals USA. Inc. North Wales, PA 19454, NDC 0703-3301-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Octreotide Acetate Injection 100 mcg/mL, 1 mL single-dose vial, Rx only, Teva Pharmaceuticals USA. Inc. North Wales, PA 19454, NDC 0703-3311-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Methylprednisolone Acetate Injectable Suspension USP, 80 mg/mL, packaged in a) 1 mL Single-Dose vials (0703-0051-01), and b) 5mL Multi Dose Vials (NDC 0703-0063-01), Rx only, TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprostadil Injection USP, 500 mg/mL, 1 mL single dose, vials, 5 mL single use vial per carton (NDC 0703-1501-02), Rx only, Teva Pharmaceuticals USA, Inc. Parsippany, NJ 07054, Vial NDC 0703-1501-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Metoclopramide Injection USP, 10 mg/2mL (5 mg/mL) 2 mL single-use vial, Rx only, Teva Parenteral Medicines, Inc. Irvine, CA 92618, NDC 0703-4502-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Adenosine Injection, USP, 60mg/20mL (3 mg/mL), 20 mL single-dose vial, Rx only, Manufactured by: Teva Pharmaceuticals USA Inc. Parsippany, NJ 07054, NDC 0703-8776-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Norepinephrine Bitartrate Injection, USP 4 mg/4 mL, 4 mL single dose vials, packaged in 10 vial cartons (NDC 0703-1153-03) Rx only, Teva Pharmaceuticals USA Inc. North Wales, PA 19454, vial NDC 0703-1153-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: August 25, 2021
Distribution: Nationwide

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Data last updated: September 15, 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.