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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
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 6,301–6,320 of 18,555 recalls

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

Data last updated:

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.