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

11401–11425 of 11827

SevereFDA (Drugs)·D-363-2013·2013-05-22
Green Valley Drugs Recalls ED Mix Injections Due to Sterility Concerns
FVS Holdings, Inc. dba. Green Valley Drugs is recalling 10,684 vials of ED Mix Injections nationwide due to a lack of assurance of sterility in compounded products.
Product
ED Mix Injections, all strengths and all presentations including a) ED mix TM -at 2, b) ED-Mix BI-Mix 10 30 mL, c) ED-Mix BI-Mix 9 30 mL; d) ED-Mix BI-Mix-3-30, e) ED-Mix PGE 80-30, f) ED-Mix SB4 30 mL, g) Ed-Mix ST 9E, h) ED-Mix ST-1, i) ED-MIX T106, j) ED-MIX-PGE-150 30 mL, k)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-346-2013·2013-05-22
Green Valley Drugs Recalls Betamethasone Combination Injection Due to Sterility Concerns
Green Valley Drugs is recalling 295 vials and syringes of Betamethasone Combination Injection because the pharmacy could not ensure the products were sterile.
Product
Betamethasone Combination Injection, all strengths and all presentations including a) Beta combo 6 mg/mL, 3 mL, b) Betameth_Combo_PF-6-2 Syr, and c) Betamethasone Combo 6 mg/mL Syr, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-391-2013·2013-05-22
Green Valley Drugs Recalls Methylprednisolone Injection Due to Sterility Concerns
Green Valley Drugs is recalling 720 syringes of Methylprednisolone, Lidocaine, and Sodium Chloride Injection because the pharmacy could not ensure the products were sterile.
Product
Methylprednisolone, Lidocaine, and Sodium Chloride Injection, all strengths and all presentations including a) Methylpred-Lido-Nacl-1-5-6-12 syringe and b) Methylpred80mg/lido1%/Sodium Chloride0.9% syr; Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-393-2013·2013-05-22
Green Valley Drugs Recalls Methylprednisolone Acetate Injection Due to Sterility Concerns
Green Valley Drugs is recalling Methylprednisolone Acetate Injection products because the company could not ensure the sterility of the compounded and repackaged items.
Product
Methylprednisolone Acetate Injection, all strengths and all presentations including a) Methylprednisolone Acetate 40 mg/mL, b) Methylprednisolone Acetate (PF) 40 mg/mL, c) Methylprednisolone Acetate (PF) 80 mg/mL, d) Methylpred Acetate 40 mg/mL 1 mL, e) Methylprednisolone 80 mg/5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-417-2013·2013-05-22
NuVision Pharmacy Recalls Methylcobalamin Injection Due to Sterility Concerns
NuVision Pharmacy is recalling 32 vials of Methylcobalamin Injection due to lack of assurance of sterility and reports of adverse events.
Product
Methylcobalamin (Buffered) Injection,1 mg/mL, 30 mL vial, Stock# 11126, Preservative Free, Compounded by NuVision Pharmacy, Inc., Dallas, TX 75244
Category
Drug
Distribution
4 states
SevereFDA (Drugs)·D-337-2013·2013-05-22
Mojo nights SUPREME Capsules Recalled for Undeclared Active Ingredients
Performance Plus Marketing, Inc. is recalling Mojo nights SUPREME Capsules because the product was marketed without an approved NDA/ANDA and may contain undeclared sildenafil, tadalafil, and analogues.
Product
Mojo nights SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC 610585435915; Distributed By: Mojo Health, Pompano Beach, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-364-2013·2013-05-22
Green Valley Drugs Recalls Estradiol Cypionate Injection Due to Sterility Concerns
Green Valley Drugs is recalling Estradiol Cypionate Injection because the pharmacy could not ensure the products were sterile. The recall covers all strengths and presentations distributed nationwide.
Product
Estradiol Cypionate Injection, all strengths and all presentations including a) Estradiol Cypionate 5 mg/mL 10 mL and b) Estradiol Cypionate 10 mg/mL 10 ml, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-341-2013·2013-05-22
Green Valley Drugs Recalls Amikacin Injection Due to Sterility Concerns
Green Valley Drugs is recalling Amikacin Injection because the pharmacy could not ensure the sterility of the compounded products. The recall covers all strengths and presentations of the drug.
Product
Amikacin Injection, all strengths and all presentations including 50, 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-353-2013·2013-05-22
Green Valley Drugs Recalls Buprenorphine Injection Due to Sterility Concerns
FVS Holdings, Inc. dba. Green Valley Drugs is recalling Buprenorphine Injection due to lack of assurance of sterility and quality control concerns.
Product
Buprenorphine Injection, all strengths and all presentations including Buprenorphine-0.3 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-372-2013·2013-05-22
Green Valley Drugs Recalls Hydrochloric Acid Injection Due to Sterility Concerns
Green Valley Drugs is recalling Hydrochloric Acid Injection products because of a lack of assurance of sterility and quality control concerns.
Product
Hydrochloric Acid Injection, all strengths and all presentations including a) Hydrochloric Acid 0.6%, b) Hydrochloric Acid 2%, c) Hydrochloric Acid Injection 0.06% 30 mL, d) Hydrochloric Acid 2 mg/mL Injection 30 mL vial, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Hend
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-398-2013·2013-05-22
Green Valley Drugs Recalls Phenylephrine Injection Due to Sterility Concerns
Green Valley Drugs is recalling Phenylephrine Injection vials because the pharmacy could not ensure the products were sterile.
Product
Phenylephrine Injection, all strengths and all presentations including Phenylephrine 1% 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-344-2013·2013-05-22
Green Valley Drugs Recalls Bacteriostatic Water for Injection Due to Sterility Concerns
Green Valley Drugs is recalling Bacteriostatic Water for Injection because the company cannot ensure the products are sterile.
Product
Bacteriostatic Water for Injection, all presentations including 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-403-2013·2013-05-22
Green Valley Drugs Recalls Pyridoxine Hydrochloride Injection for Sterility Concerns
Green Valley Drugs is recalling Pyridoxine Hydrochloride Injection due to lack of assurance of sterility and quality control concerns.
Product
Pyridoxine Hydrochloride Injection, all strengths and all presentations including Pyridoxine 100 mg/mL 30 mL, 50 mL, and 10 mL PF SDV, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-388-2013·2013-05-22
Green Valley Drugs Recalls Methylprednisolone and Marcaine Injections for Sterility Concerns
FVS Holdings, Inc. dba. Green Valley Drugs is recalling 607 vials of Methylprednisolone Acetate and Marcaine Injection due to lack of assurance of sterility and quality control concerns.
Product
Methylprednisolone Acetate and Marcaine Injection, all strengths and all presentations including a) Methylpred 80 mg/mL and Marcaine 0.25%-2.75, b) Methylpred_Marc-0.25-0.27, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-380-2013·2013-05-22
Green Valley Drugs Recalls Lipotropic Injections Due to Sterility Concerns
FVS Holdings, Inc. dba. Green Valley Drugs is recalling 209 vials of Lipotropic With Vitamin Injections nationwide due to a lack of assurance of sterility.
Product
Lipotropic With Vitamin Injections, all strengths and all presentations including a) Lipo W/ Vitamin 100 mL, b) Lipo W/ Vitamins 30 mL, c) Lipo W/Vitamin, d) Lipo w/Vitamins #5 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-379-2013·2013-05-22
Green Valley Drugs Recalls Lidocaine Injections Due to Sterility Concerns
Green Valley Drugs is recalling Lidocaine Injection products because the pharmacy could not ensure the sterility of the compounded and repackaged items.
Product
Lidocaine Injection, all strengths and all presentations including a) Lidocaine _HCl-0.5%, b) Lidocaine HCl, c) Lidocaine 1%, d) Lidocaine 1% 50 mL, e) Lidocaine 2 %, f) Lidocaine 2% 50 mL, g) Lidocaine 2% 50 mL MDV, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-400-2013·2013-05-22
Green Valley Drugs Recalls Polidocanol Injection Due to Sterility Concerns
Green Valley Drugs is recalling Polidocanol Injection vials nationwide due to a lack of assurance of sterility and quality control concerns.
Product
Polidocanol Injection, all strengths and all presentations including a) Polidocanol 5% 30 mL, b) Polidocanol 1% 30 mL, c) Polidocanol 2% 30 mL, d) Polidocanol 3% 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-408-2013·2013-05-22
Green Valley Drugs Recalls Sodium Chloride Injection Due to Sterility Concerns
Green Valley Drugs is recalling 318 vials of Sodium Chloride Injection due to a lack of assurance of sterility and quality control concerns.
Product
Sodium Chloride Injection, all strengths and all presentations including a) Bacteriostatic Sodium Chloride 0.9% 30 mL, b) Sodium Chloride 23.4% 30 mL PF, and c) Sodium Chloride 23.4% 50 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-409-2013·2013-05-22
Green Valley Drugs Recalls Sodium Tetradecyl Sulfate Injection for Sterility Concerns
Green Valley Drugs is recalling 203 vials of Sodium Tetradecyl Sulfate Injection due to lack of assurance of sterility and quality control concerns.
Product
Sodium Tetradecyl Sulfate Injection, all strengths and all presentations including a) Sodium Tetradecyl Sulfate 3% 50 mL, b) Sodium Tetradecyl Sulfate 3% mL, c) Sodium Tetradecyl Sulfate-2% 30 mL, d) Sodium Tetradecyl Sulfate-2.5% 20 mL, e) Sodium Tetradecyl Sulfate 0.3% 30 mL, f
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-327-2013·2013-05-22
Evol Nutrition Recalls Mojo Nights Capsules for Unapproved Ingredients
Evol Nutrition is recalling Mojo Nights capsules because they contain unapproved ingredients used to treat erectile dysfunction.
Product
Mojo Nights, 1 capsule, UPC 7 18122 11983 7, Distributed By: Mojo Health Lauderhill, FL 33351
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-413-2013·2013-05-22
Green Valley Drugs Recalls Testosterone Cypionate Injection Due to Sterility Concerns
Green Valley Drugs is recalling Testosterone Cypionate Injection vials and syringes because the compounding pharmacy could not ensure the products were sterile.
Product
Testosterone Cypionate Injection, all strengths and all presentations including a) Testosterone Cyp 200 mg/10 mL; b) Testosterone Cypionate 100 mg/10mL; c) Testosterone Cypionate 200 mg 10 mL; d) Testosterone Cypionate 200 mg 30 mL; e) Testosterone Cypionate 200 mg/mL; f) Testo
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-387-2013·2013-05-22
Green Valley Drugs Recalls Methylcobalamin Injections Due to Sterility Concerns
Green Valley Drugs is recalling 1,343 vials of Methylcobalamin Injection nationwide because the pharmacy could not ensure the products were sterile.
Product
Methylcobalamin Injection, all strengths and all presentations including a) Methylcobalamin 1000 mcg/mL in 10 mL, 30 mL, 50 mL, 60 mL, b) Methylcobalamin 1000 mcg 30 mL, c) Methylcobalamin 5 mg/mL 30 mL, d) Methylcobalamin PF 1000 mcg/mL in 2 mL, 5 mL, 10 mL, Rx only, Green Valle
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-399-2013·2013-05-22
Green Valley Drugs Recalls Phosphatidylcholine Injection Due to Sterility Concerns
Green Valley Drugs is recalling Phosphatidylcholine and Sodium Deoxycholate Injection due to a lack of assurance of sterility in compounded products.
Product
Phosphatidylcholine and Sodium Deoxycholate Injection, all strengths and all presentations including Phospha_Deoxy-35-30-50 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-339-2013·2013-05-22
FDA Recalls Acetylcysteine Injection Due to Sterility Assurance Concerns
Green Valley Drugs is recalling Acetylcysteine Injection vials because the pharmacy could not ensure the products were sterile.
Product
Acetylcysteine Injection, all strengths and all presentations including 100 mg/mL in 30 mL vials and 200 mg/mL in 30 mL and 50 mL vials, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-366-2013·2013-05-22
Green Valley Drugs Recalls Folic Acid Injections Due to Sterility Concerns
Green Valley Drugs is recalling 244 vials of Folic Acid Injection nationwide due to a lack of assurance of sterility in its compounding and quality control processes.
Product
Folic Acid Injection, all strengths and all presentations including a) Folic Acid 10 mg/mL 30 mL; b) Folic Acid PF 10 mg/mL 2 mL and 5 mL; c) Folic Acid 20 mg/mL 30 mL; d) Folic Acid 5 mg/mL 5 mL, 10 ml and 30 mL Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV
Category
Drug
Distribution
Distributed nationwide

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11401–11425 of 11827