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Recall totals

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

37,341

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

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 2,095 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 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 October 29, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

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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FDA Recall TerminatedTerminated: May 17, 2023Historical recordClass II

Dr. Berne's MSM DROPS 15% Solution, Net Wt. 30ml/1.014 OZ, Distributed by: Dr. Berne's Whole Heallth Products, 400 Hillsboro Technology Drive, Deerfield BEach, FL 33441 SKU#182 UPC 00854582001036

by MSM Nutraceuticals, LLC

Reason: Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 17, 2023Historical recordClass II

Red Eye, Eye Drops, Active Ingredients: OptiMSM, Glycerin USP, Hyaluronic Acid, Naphazolene Chloride, Net Wt. 15ml, 0.15 fl oz., Manufactured by: MSM Nutraceuticals, LLC , UPC 8 54582 00118 0

by MSM Nutraceuticals, LLC

Reason: Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 17, 2023Historical recordClass II

Dry Eye, Eye Drops, Active Ingredients: OptiMSM, Glycerin USP, Hyaluronic Acid, Polyethylene Glycon, Net Wt. 15ml, 0.51 fl oz., Manufactured by: MSM Nutraceuticals, LLC, UPC 8 54582 00119 7.

by MSM Nutraceuticals, LLC

Reason: Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 17, 2023Historical recordClass II

15% MSM, Eye Drops, Net Wt. 30ml, 1.014 oz., Manufactured by: MSM Nutraceuticals, LLC 2103 West Parkside Lane, Ste.107, Phoenix, AZ 85027, UPC 8 54582 00120 3.

by MSM Nutraceuticals, LLC

Reason: Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Published: April 24, 2019
Distribution: Nationwide

View recall →

Data last updated: October 29, 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.