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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 2026

Most affected stateHawaii 200 recalls mention this state

State: MD ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 11, 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	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Bi-Est (estriol,estradiol), Progesterone, Testosterone cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Estradiol cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Bi-Est (estriol,estradiol) Testosterone cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Estriol,Estradiol cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Bi-Est (estriol,estradiol), Progesterone, DHEA, Testosterone drops, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Estradiol, Estriol capsules, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Estradiol, Estriol, Progesterone capsules, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Tri-Est 80:10:10 Progesterone (estriol, estradiol, estrone, progesterone) capsules Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 29, 2016Historical recordClass II

Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811

by Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Reason: Failed Dissolution Specifications
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 7, 2016Historical recordClass III

ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603-2116-28

by Qualitest Pharmaceuticals

Reason: Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Methyl Folate Lyophilized Powder for Injection, 20 mg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Chorionic Gonadotropin/ Hydroxocobalamin Lyophilized Powder Injectable, 10,000 UNITS/ 5000 mcg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Artesunate Lyophilized Powder for Injection, 60 mg per vial, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Meloxicam capsules, 12 mg, Rx Only, Manufactured by Park Compounding, Irving, CA -non-sterile formulation

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Leucovorin Calcium capsules, 10 mg, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 31, 2016Historical recordClass II

Bi-Est 80:20 Progesterone (estriol,estradiol, progesterone) capsules, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 15, 2016Historical recordClass III

Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/80 mg, 30 Count Bottles, Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. NDC: 43598-313-30.

by Dr. Reddy's Laboratories, Inc.

Reason: Subpotent Drug: Subpotent atorvastatin.
Published: September 2, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2016Historical recordClass III

Amlodipine besylate and Atorvastatin calcium Tablets,10 mg/40 mg, Packaged in a) 30 Count Bottles (NDC: 43598-315-30) and b) 90 Count Bottles (NDC: 43598-315-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India.

by Dr. Reddy's Laboratories, Inc.

Reason: Subpotent Drug: Subpotent atorvastatin.
Published: September 2, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2016Historical recordClass III

Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) and b) 90 Count Bottles (NDC: 43598-318-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India

by Dr. Reddy's Laboratories, Inc.

Reason: Subpotent Drug: Subpotent atorvastatin.
Published: September 2, 2015
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2016Historical recordClass III

Amlodipine besylate and Atorvastatin calcium Tablets, 5 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-319-30) and b) 90 Count Bottles (NDC: 43598-319-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India.

by Dr. Reddy's Laboratories, Inc.

Reason: Subpotent Drug: Subpotent atorvastatin.
Published: September 2, 2015
Distribution: Nationwide

View recall →

Data last updated: November 11, 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.