Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

5401–5425 of 8593

SevereFDA (Drugs)·D-0183-2016·2015-11-18
FDA Recalls Compounder Biest Troches Due to Penicillin Cross-Contamination
The Compounder is recalling Biest 80/20 troches because an active ingredient was contaminated with penicillin. Patients should stop using the product and consult their healthcare provider.
Product
BIEST 80/20 : PROGEST : DHEA : TESTOST (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow): Progesterone USP: Dehydroepiandrosterone Micronized (DHEA): Testosterone Trit ) 2.5 : 25 : 2.5 : 0.1MG TROCHE, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0206-2016·2015-11-18
The Compounder Recalls Biest TD 80/20 Cream Due to Penicillin Contamination
The Compounder is recalling Biest TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
Product
BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) W/V (weight/volume) 1.25:100:0.625 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only,The Compounder, 340 Marshall
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0172-2016·2015-11-18
B&B Pharmacy Recalls PAPA/PGE1/PHENTO Injection Due to Sterility Concerns
Pacific Healthcare, Inc dba B&B Pharmacy is recalling PAPA/PGE1/PHENTO injection vials because an FDA inspection identified GMP violations that may impact product sterility.
Product
PAPA/PGE1/PHENTO (30mg/50mcg/0.5mg/ml), Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflower, CA
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0218-2016·2015-11-18
FDA Recalls Compounder Transdermal Cream Due to Penicillin Contamination
The Compounder is recalling specific lots of a compounded transdermal hormone cream because the active ingredient was contaminated with penicillin.
Product
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,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0223-2016·2015-11-18
The Compounder Recalls Estriol Cream Due to Penicillin Cross-Contamination
The Compounder is recalling specific lots of Estriol transdermal cream because the active ingredient was contaminated with penicillin.
Product
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.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0215-2016·2015-11-18
The Compounder Recalls Estradiol Cream Due to Penicillin Cross-Contamination
The Compounder is recalling Estradiol, Progesterone, and DHEA transdermal cream because the active ingredient was contaminated with penicillin.
Product
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.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0180-2016·2015-11-18
PGE 25mcg/ml Injection Recalled Due to Sterility Assurance Concerns
Pacific Healthcare, Inc dba B&B Pharmacy is recalling PGE 25mcg/ml Injection vials because an FDA inspection identified GMP violations that may impact sterility.
Product
PGE 25mcg/ml, Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflower, CA
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0179-2016·2015-11-18
B&B Pharmacy Recalls PAPA/PGE1/PHENTO Injection Due to Sterility Concerns
Pacific Healthcare, Inc dba B&B Pharmacy is recalling PAPA/PGE1/PHENTO injection vials because an FDA inspection found GMP violations that may affect sterility.
Product
PAPA/PGE1/PHENTO (35mg/12mcg/1.5mg/ml), Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflower, CA
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0199-2016·2015-11-18
The Compounder Recalls BIEST TD 80/20 Cream Due to Penicillin Contamination
The Compounder is recalling BIEST TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
Product
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
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0175-2016·2015-11-18
B&B Pharmacy Recalls PAPA/PGE1/PHENTO Injection Due to Sterility Concerns
Pacific Healthcare, Inc dba B&B Pharmacy is recalling PAPA/PGE1/PHENTO Injection vials because an FDA inspection identified GMP violations that may impact product sterility.
Product
PAPA/PGE1/PHENTO (30mg/40mcg/1mg/ml) Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflower, CA
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0193-2016·2015-11-18
The Compounder Recalls Biest TD 80/20 Cream Due to Penicillin Contamination
The Compounder is recalling Biest TD 80/20 transdermal cream because the active ingredient was contaminated with penicillin. Patients should stop using the product and consult their healthcare provider.
Product
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.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0197-2016·2015-11-18
The Compounder Recalls BIEST TD 80/20 Cream Due to Penicillin Contamination
The Compounder is recalling BIEST TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
Product
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 prefi
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0214-2016·2015-11-18
The Compounder Recalls Estriol Capsules Due to Penicillin Contamination
The Compounder is recalling Estriol 4.0mg capsules because the active ingredient was contaminated with penicillin. Patients should stop using the product and consult a healthcare provider.
Product
ESTRIOL (E3) 4.0MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0192-2016·2015-11-18
The Compounder Recalls Biest TD 80/20 Transdermal Cream Due to Penicillin Contamination
The Compounder is recalling Biest TD 80/20 transdermal cream because the active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
Product
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.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0105-2016·2015-11-04
Moses Lake Pharmacy Recalls Methylcobalamin Injectable Solution Due to Sterility Concerns
JD & SN Inc. is recalling specific syringes of Methylcobalamin Injectable Solution because the FDA cannot assure the sterility of the compounded drug.
Product
METHYLCOBALAMIN MDV, Injectable Solution, 1 MG/ML, syringe sizes: 4 mL; 10 mL; 12 mL; 15mL; 30 mL; 50 mL; and 60 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0151-2016·2015-11-04
Moses Lake Pharmacy Recalls Trimix Injectable Solution Due to Sterility Concerns
Moses Lake Professional Pharmacy is recalling Trimix injectable solution because the FDA cannot assure the sterility of the compounded drug.
Product
TRIMIX, injectable Solution, 30MG/2MG/20MCG, syringe size: 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0088-2016·2015-11-04
FDA Recalls Estradiol Pellets Due to Lack of Sterility Assurance
The FDA is recalling Estradiol pellets compounded by Moses Lake Professional Pharmacy because the firm cannot assure the sterility of the product.
Product
ESTRADIOL, Pellet, 9 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0118-2016·2015-11-04
FDA Recalls Compounded Progesterone Pellets Due to Sterility Concerns
The FDA is recalling compounded progesterone pellets from Moses Lake Professional Pharmacy because the agency cannot ensure the products are sterile.
Product
PROGESTERONE, Pellet, 50mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0078-2016·2015-11-04
FDA Recalls Estradiol Pellets Due to Lack of Sterility Assurance
JD & SN Inc. is recalling Estradiol pellets because the FDA determined there is a lack of assurance of sterility for all sterile human compounded drugs within their expiry.
Product
ESTRADIOL, Pellet, 12.5 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0056-2016·2015-11-04
Moses Lake Pharmacy Recalls Alprostadil/Procaine Injectable Solution for Sterility Concerns
JD & SN Inc. is recalling 150 vials of Alprostadil/Procaine Injectable Solution due to a lack of assurance of sterility.
Product
ALPROSTADIL/PROCAINE, Injectable Solution, 20 MCG/0.1%/ML, 10 mL vial, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0149-2016·2015-11-04
Moses Lake Pharmacy Recalls TRIMIX Injectable Solution Due to Sterility Concerns
JD & SN Inc. is recalling TRIMIX injectable solution because the agency could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
Product
TRIMIX, injectable Solution, 30MG/1MG/10MCG, syringe sizes: 5 mL and 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0154-2016·2015-11-04
Moses Lake Pharmacy Recalls Vitamin D3 Injectable Solution for Sterility Concerns
JD & SN Inc. is recalling 4 syringes of Vitamin D3 Oil Injectable Solution due to a lack of assurance of sterility.
Product
VITAMIN D3 OIL, Injectable Solution, 400,000 UNITS/ML, syringe size: 20 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0064-2016·2015-11-04
Moses Lake Pharmacy Recalls Chorionic Gonadotropin Due to Sterility Concerns
JD & SN Inc. is recalling specific vials of Chorionic Gonadotropin because the FDA cannot assure the sterility of the compounded drug.
Product
CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0.1 ML, vial sizes: 4 mL; 5 mL; 6 mL; 7.5 mL ; 9 mL, 10 mL; 12 mL; 15 mL; 20 mL; 28 mL; Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0142-2016·2015-11-04
Moses Lake Pharmacy Recalls Testosterone Cypionate Injection Due to Sterility Concerns
Moses Lake Professional Pharmacy is recalling Testosterone Cypionate for Subcutaneous Injection because the product lacks assurance of sterility.
Product
TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 100 mg/mL, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0141-2016·2015-11-04
Moses Lake Pharmacy Recalls Compounded Testosterone Cypionate Injectable Solution
Moses Lake Professional Pharmacy is recalling compounded Testosterone Cypionate injectable solution due to a lack of assurance of sterility.
Product
TESTOSTERONE CYPIONATE (COMPOUNDED), Injectable Solution, 200 MG/ML, syringe sizes: 5mL and 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide

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5401–5425 of 8593