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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 40 Day Injection Extra Strength, vials, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 4,100 Units/vial Injection, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 23 Day Injection Extra Strength, vials, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN 1-800-263-8890

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 20,000 units/vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 20 Day Extra Strength, 3500 Units/4 mL, 10 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 30 Day, 3750 Units/6 mL, 10 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN 1-800-263-8890

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 23 Day, 2876 Units/4.6 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 20 Day Injection, 2625 Units/4 mL, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 11,000 Units, 30 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

HCG 1,000 U/mL Injection, 30 mL, Vial Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Gentamicin 250 mg/1000 mL Irrigation, 1000 mL, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Gentamicin 120 mg/250 mL 0.9% Sodium Chloride for Irrigation, 30 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Estradiol Cypionate 10 mg/mL, 5 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

DMSO 50% 60 mL/Heparin 1 mL/ Sodium Bicarbonate 60 mL/ Solu-Cortef 100 mg, 41 mL syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Dexamethasone 24 mg/mL Injection, 10 mL Vial, Anderson Compounding Pharmacy, 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Vancomycin 125 mg/3mL Inhalation, 3 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Amphotericin B 0.15% Eye Drops, 2 mL Droppers, Anderson Compounding Pharmacy 310 Bluff City Hwy Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Atropine 0.01% Eye Drops, 1 mL and 2 mL Dropper, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Acetylcysteine 10% Ophthalmic Eye Drop 2 mL droptainer, Anderson Compounding Pharmacy 310 Bluff City Hwy Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason: Lack of sterility assurance.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 13, 2025Historical recordClass III

Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022

by Estee Lauder Inc

Reason: Defective container: Ineffective seal between the cap and jar of the affected product.
Published: April 24, 2019
Distribution: Nationwide

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Data last updated: November 8, 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.