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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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 September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) IN VERSABASE W/V (weight/volume) 4 : 67.5 :10MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) IN VERSABASE W/V (weight/volume) 2.5 : 25 :1.25MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 6.5 : 30: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 3: 25: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) 2.5 : 20 : 1.25 : 0.25 MG/ML TRANSDERMAL (Cream)Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 5.0 : 30 : 2.5 : 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized): DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 2.5: 30 : 2.5 : 0.25 MG/MLTransdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (yellow) / Estriol USP Micronized (E3)): PROG (Progesterone USP Micronized) W/V 2.5MG:100MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) W/V(weight/volume) [2977] 6.25MG/ML Transdermal cream, dispensed in 1 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) W/V (weight/volume) 5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) W/V (weight/volume) 2.5MG/ML Transdermal cream, dispensed in a) 3 mL and b) 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 12.5 MG/ML 1.25MG/0.1ML Transdermal cream, dispensed in 1 mL prefilled, amber syringes,Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 8 MG/ML transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 67/33 (Estradiol (E2) TRIT (YELLOW)/Estriol USP Micronized (E3)) W/V (weight /volume) 1.5 MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 4.0 MG/ML transdermal cream packaged in 3mL syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cream, dispensed in 10 mL prefilled syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST CP 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) 2.5 MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST CP 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) 1.25 MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BIEST CP 76/24: DHEA (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow) : Dehydroepiandrosterone Micronized (DHEA) 2.625 MG : 10 MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Published: November 18, 2015
Distribution: Nationwide

View recall →

Data last updated: September 30, 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.