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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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

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Source: FDA and USDA public dataLast updated September 14, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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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FDA Recall Terminated Historical recordClass II

Epoprostenol Sodium for Injection, 1.5 mg/vial, 10 mL vials, Rx only, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0703-1995-01

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, Teva Parenteral Medicines, Inc. Irvine, CA 92618, NDC 0703-5145-01

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 1000 mcg/5mL, 5 mL multi-dose vial, Rx only, Teva Pharmaceuticals USA. Inc. North Wales, PA 19454, NDC 0703-3333-01

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

Vecuronium Bromide for Injection 10 mg, 10mL vial, Rx only, Teva Pharmaceuticals USA, North Wales, PA 19454, NDC 0703-2914-01

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

Idarubicin Hydrochloride Injection 20 mg/20 mL, 20 mL single-dose vial, Rx only, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0703-4156-11

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

Amikacin Sulfate Injection USP 1 gram/4mL (250mg/ML), 4 mL single-dose vials, Rx only, Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0703-9040-01

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

Haloperidol Decanoate Injection 100 mg/mL, packaged in a) 1 mL single-dose vials (NDC 0703-7131-01), b) 5 mL multi-dose vials (NDC 0703-7133-01), 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

Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, packaged in a) 1 mL Single-Dose vials (0703-0031-01), and b) 5mL Multi Dose Vials (NDC 0703-0043-01), and c) 10 mL Multi-Dose Vials (NDC 0703-0045-01), 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

DAUNOrubicin Hydrochloride Injection 20 mg/4mL, 4mL Single Dose vials, 10 in 1 carton, Rx only, Teva Parenteral Medicines, Inc. Irvine, CA 92618 Vial NDC# 0703-5233-11, Carton NDC # 0703-5233-13

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

Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10

by Spirit Pharmaceuticals

Reason: cGMP deviations: Discolored acetaminophen
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Avicel, Mirocrystalline cellulose, packaged in bulk as PH101 NF, PH102 NF, PH200 NF, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711

by DuPont Nutrition USA, Inc

Reason: Out of specification results for conductivity.
Published: August 25, 2021
Distribution: Nationwide

View recall →

Data last updated: September 14, 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.