Public Health Trace

Get Alerts

Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,205

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/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 2026

Most affected stateHawaii 200 recalls mention this state

State: NE ×
Clear all

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated October 2, 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).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
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 III

Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-035-01) and b) 1000 Ct Bottles (NDC: 49884-035-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.

by Par Pharmaceutical Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification for impurities.
Published: November 25, 2015
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7 538073516768.

by The One Minute Miracle Inc

Reason: Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain undeclared phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules per carton, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 0911312397354.

by The One Minute Miracle Inc

Reason: Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain undeclared thiosildenafil, an analogue of an FDA approved drug for male erectile dysfunchtion making this product an unapproved drug.
Published: November 18, 2015
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

TRIEST 80/10/10 (Estrone (E1) Trit / Estradiol (E2) Trit / Estriol USP (E3)) 1.875MG 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

TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol USP (E3)) (23) 5MG 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

TRIEST 70/20/10 ( Estriol USP / Estradiol USP (E2) / Estrone (E1) Triturate) [909] 12.5MG/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

ESTRIOL 5 ESTRADIOL (Estradiol (E2) Trit (Yellow)) 0.95 ESTRONE (Estrone E1) Trit (Red)) 0.02 TEST (Testosterone USP) 0.75MG/ML W/V (weight/volume) 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

ESTRIOL (E3) W/V (weight/volume) VERSABASE [4714] 0.05% (0.5MG/ML) transdermal cream, dispensed in a) 1 mL and b) 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

ESTRIOL (E3) W/V (weight/volume) VERSABASE 3MG/ML Transdermal cream, dispensed in 5 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

ESTRIOL (E3) W/V (weight/volume) PGF 0.1% (1.0MG/ML) Transdermal cream, is 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

ESTRIOL (E3) 2.5MG suppositories, 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

ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/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

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : TESTO (Testosterone USP) W/V (weight/volume) 2.0: 0.1: 0.5MG/ML Transdermal cream, dispensed in 5 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

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 30 : 0.5 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

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 35 : 0.5 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

ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 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

ESTRIOL (E3) : PROGESTERONE : DHEA (Dehydroepiandrosterone Micronized) W/V (weight/volume) VERSABASE 4.0 : 30 : 4MG/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

ESTRIOL (E3) 4.0MG 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

E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized (E3) : PROGEST (Progesterone USP Micronized) : TESTOST (Testosterone USP) IN OLIVE OIL 0.75 : 3 : 50 : 5MG 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 TD 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) : PROGESTERONE W/V (weight/volume) PLO (Pluronic F127 20% or Polox 20% gel) 3.3 MG/ML : 40 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 →

Data last updated: October 2, 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.