Medicines, 2015
Shortlist up to four to read them side by side.
2,020 medicine recalls FDA’s Enforcement Report published in 2015, newest first; 18,075 in all since 2012.
FDA’s medicine recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 5, 2026.
2,020of 2,020 medicine recallsshown with your filters
The list
- Medicine recall BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized)… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized)… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : TESTO (Testosterone USP) W/V… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) VAN CR (vanishing cream) W/V… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 83/17 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) 1.2 MG/ML… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 86/14 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) IN PLO GEL (Pluronic F127 20% or… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 89/11 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) VERSABASE… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall BIEST TD 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) : PROGESTERONE W/V (weight/volume)… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized (E3) : PROGEST (Progesterone USP Micronized) :… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) 4.0MG capsules Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) : PROGESTERONE : DHEA (Dehydroepiandrosterone Micronized) W/V (weight/volume) VERSABASE 4.0 : 30… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 MG/ML Transdermal cream, dispensed Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : TESTO (Testosterone USP) W/V (weight/volume)… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/ML Transdermal cream, dispensed Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) 2.5MG suppositories Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) W/V (weight/volume) PGF 0.1% Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) W/V (weight/volume) VERSABASE 3MG/ML Transdermal cream, dispensed Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL (E3) W/V (weight/volume) VERSABASE [4714] 0.05% Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ESTRIOL 5 ESTRADIOL (Estradiol (E2) Trit (Yellow)) 0.95 ESTRONE (Estrone E1) Trit (Red)) 0.02 TEST… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall TRIEST 70/20/10 ( Estriol USP / Estradiol USP (E2) / Estrone (E1) Triturate) [909] 12.5MG/ML transdermal… Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol USP (E3)) Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall TRIEST 80/10/10 (Estrone (E1) Trit / Estradiol (E2) Trit / Estriol USP (E3)) 1.875MG capsules Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Class IIFDA’s classNov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall MIRACLE ROCK 48 capsules 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… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IStatusOngoingWhereNationwide
- Medicine recall MIRACLE DIET 30 capsules, 30-count bottle Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain undeclared phenolphthalein, a drug product once contained in over-the-counter… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 18, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 18, 2015ClassClass IStatusOngoingWhereNationwide
- Medicine recall RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL Failed Stability Specifications: Out of Specification results obtained for preservative butylparaben. Class IIIFDA’s classNov 11, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2015ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle Failed Dissolution Specifications: Failed 24 month dissolution testing. Class IIFDA’s classNov 11, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ALPROSTADIL, Injectable Solution, 40 MCG/ML, 10 mL vials Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ALPROSTADIL/PROCAINE, Injectable Solution, 20 MCG/0.1%/ML, 10 mL vial Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall ALPROSTADIL/PROCAINE, Injectable Solution, 40 MCG/0.1%/ML, 10 mL and 20 mL vials Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall B1/B2/B3/B5/B12/LIDOCAINE/ISOLEUCINE/METHIONINE/CHOLINE/INOSITOL, Injectable Solution,… Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall B1/B2/B5/B12/LIDOCAINE/ISOLEUCINE/METHIONINE/CHOLINE/INOSITOL, Injectable Solution, 50/5/5/1/10/25/8/17/17… Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CALM ME VITAMIN COCKTAIL, MAGNESIUM, COMPOUNDED B COMPLEX, Injectable Solution, 30 mL vial Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN, Injectable Solution, 4000 UNITS/ mL, 8 mL vial Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN, Injectable Solution, 1000 UNITS/0.1 mL, 1 mL vial Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN, Injectable Solution,175 UNITS/1.5mg per syringe with Methylcobalamin Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0.1 ML, vial sizes: 4 mL Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN, Injectable Solution, 5000 UNITS/0.1 mL, vial sizes: 5 mL Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 150 UNITS/0.150 ML per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 200 UNITS/0.2ML per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 250 UNITS/0.25ML per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 500 UNITS/0.5ML per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN/CYANOCOBALAMIN, Injectable Solution, 1000 units/1 mL per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CHORIONIC GONADOTROPIN/CYANOCOBALAMIN, Injectable Solution, 2000 unit/1mg/mL per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CYANOCOBALAMIN MDV (COMPOUNDED), Injectable Solution, 1 MG/ML per syringe Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall DEXPANTHENOL, Injectable Solution, 250 MG/ML, 30 mL syringes Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Class IIFDA’s classNov 4, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 4, 2015ClassClass IIStatusTerminatedWhereNationwide
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Drug recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
Your shortlist0 of 4
Add one more to compare.