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

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Source: FDA and USDA public dataLast updated September 18, 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

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

KETAMINE 50 MG/ML (NPV) INJECTION SOLUTION (C-III), 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Inositol/Choline B12:B6, 50/50/1/0.175 MG/ML INJ SOLN(Sulfa Free Lipostat), 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0999-30

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GLUTATHIONE 200MG/ML (PFV) INJECTION SOLN, 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0971-81

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

FOLIC ACID 5MG/ML INJECTION SOLUTION (MDV), 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0924-10

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine 1:1000 INJECTION SOLUTION (PF) Syringe, 1 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0947-01

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EDETATE DISODIUM 15% INJECTABLE, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0922-30

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EDETATE CALCIUM DISODIUM 150MG/ML INJECTABLE, 100 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0934-11

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

DIMERCAPTO-PROPANESULFONIC 5% (DMPS)( (PFV) INJ SOL, 5 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0904-05

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CYANCOBALAMIN 1200MCG/ML MDV INJECTION, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0946-30

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Copper 0.4MG/ML (PVF) INJECTION SOLUTION, 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0925-10

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BUFFERED LIDOCAINE 1%+EPI 1:100,000 INJ SOL, [3ML NDC: 70731-0137-03 and 30ML NDC: 70731-0137-30] per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0137-03

by RXQ Compounding LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ascorbic Acid 500 MG/ML (Non-Corn) INJ (MDV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0975-50

by RXQ Compounding LLC

Reason: Crystallization
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ascorbic Acid 400 MG/ML (Non-Corn) Injection Solution, 65 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0914-65

by RXQ Compounding LLC

Reason: Crystallization
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10

by RXQ Compounding LLC

Reason: Crystallization
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CVS Health Children's Nasal Saline Drops with Himalayan Salt Saline Nasal Moisturizer, 30 single-use vials per Carton,0.05 fl. oz. (1.5 mL) each 1.5 fl. oz. (45 mL) total, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, UPC 050428598207

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Appetrol Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Mental Tonic Capsules, Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyro-Lo, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyro-H, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Stone Purger Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published: August 14, 2019
Distribution: Nationwide

View recall →

Data last updated: September 18, 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.