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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

State: GU ×
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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

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

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FDA Recall Terminated Historical recordClass II

Cholestene capsules, 1200 mg of red yeast rice per 2 capsules, 120-count bottle, Manufactured by: High Performance Formulas, L.L.C. (HPF, L.L.C.) P.O. Box 1311, Morrisville, PA 19067, UPC 640485-10093-4

by High Performance Formulas, L.L.C. (HPF, L.L.C.)

Reason: Marketed Without an Approved NDA/ANDA
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GaviLyteTM - C PEG-3350 (240g) and Electrolytes for Oral Solution, USP with Flavor Pack Manufactured by Novel Laboratories, Inc. Somerset, NJ 08873, USA Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 NDC 43386-060-19

by Novel Laboratories, Inc. d.b.a LUPIN

Reason: Failed Stability Specification; Out of specification for Osmolarity
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg per day 50/250 Twice Weekly Rx Only a) 2 Systems NDC 68968-0525-2; b) 8 Systems NDC 68968-0525-8, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186, Dist. by: Noven Therapeutics LLC, Miami, Florida 33186

by Noven Pharmaceuticals Inc

Reason: Failed Stability Specifications; out of specification for shear.
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg per day, 50/140 Twice Weekly, Rx Only a) 2 Systems NDC 68968-0514-2 b) 8 Systems NDC 68968-0514-8, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186, Dist. by: Noven Therapeutics LLC, Miami, Florida 33186

by Noven Pharmaceuticals Inc

Reason: Failed Stability Specifications; out of specification for shear.
Published: August 25, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ethosuximide Oral Solution USP 250 mg/5 mL, 16 fl oz (473 mL), Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0670-16

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason: Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cimetidine Hydrochloride Oral Solution 300 mg/5 mL, 8 fl oz (237 mL) Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0649-08

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason: Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nystatin Oral Suspension, USP 100,000 units per mL, Cherry/Peppermint Flavor, Rx ONLY, packaged in a) 16 fl oz (473 mL) NDC 0121-0868-16; b) 2 fl oz (60 mL) NDC 0121-0868-02; Manufactured by: Pharmaceutical Associates, Inc. Greenville, SC 29605

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason: Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg Double Strength, 500 Tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-HIghtstown Road, EAs Windsor, NJ 08520, Made in India, NDC 65862-420-05

by Aurobindo Pharma USA Inc.

Reason: Presence of Foreign Substance- Potential of metal contamination.
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

5000 Years Foods, Inc.

Product: 5000 Years Foods BABY NAPA KIMCHI in 128 oz, 64 oz, and 32 o…
Reason: potential to be contaminated with Listeria monocytogenes
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

5000 Years Foods, Inc.

Product: 5000 Years Foods WHITE WHOLE KIMCHI in 128 oz, 64 oz, and 32…
Reason: potential to be contaminated with Listeria monocytogenes
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

5000 Years Foods, Inc.

Product: 5000 Years Foods NO MSG JULRADO SLICED CABBAGE KIMCHI in 128…
Reason: potential to be contaminated with Listeria monocytogenes
Published: August 18, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

5000 Years Foods, Inc.

Product: 5000 Years Foods NO MSG JULRADO WHOLE CABBAGE KIMCHI in 128…
Reason: potential to be contaminated with Listeria monocytogenes
Published: August 18, 2021
Distribution: Nationwide

View recall →

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.