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  1. FDA Recalls
  2. ›Drug Recalls

FDA Drug Recalls

Recalls of prescription drugs, over-the-counter medications, and compounded pharmaceuticals.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 11061–11080 of 17,816 recalls

Class IIOngoing

TriMix, Alprostadil/Phentolamine/Papaverine 30mcg/1mg/10mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IIOngoing

Dexpanthenol 250 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class II
Ongoing

Calm Me (Aminobutyric Acid (GABA) 50 mg/Magnesium Chloride 50 mg/Taurine 50 mg/Theanine (L) 50 mg/Tryptophan (L) 10 mg/Lidocaine HCL 10 mg/ml), (30 ML). Compounded by Tri-Coast Pharmacy.

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IIOngoing

L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IIOngoing

HCG 11,000 IU Vial. Compounded by Tri-Coast Pharmacy

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IIOngoing

HCG 5,000 IU Vial. Compounded by Tri-Coast Pharmacy.

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IIOngoing

Amino Acid Recover Eaze (50 ML), Phenylaline (L) 8 mg/ml + Tyrosine (L) 0.45 mg/ml + L-Taurine 0.7 mg/ml. Compounded by Tri-Coast Pharmacy.

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IIOngoing

Amino Energy Cocktail (30 ML), (Methionine (L) 12.5 mg/Inositol 25 mg/Choline Chloride 25 mg/Methylcobalamin 300 mcg/Carnitine (L) 125 mg/Thiamine HCL 50 mg/Riboflavin-5-Phosphate Sod 5 mg/Niacinamide 20 mg/Pyridoxine HCL 2 mg/Folic Acid 2 mg/Ascorbic Acid 50 mg/Chromium Picolinate 200 mcg/Glutamine (L) 30 mg/Lidocaine HCL 10 mg/mL). Compounded by Tri-Coast Pharmacy.

Tri-Coast Pharmacy

Lack of Assurance of Sterility

November 17, 2016 · DrugView details →
Class IITerminated

Desoximetasone Ointment USP, 0.25%, a) 15 g tubes (NDC 61748-206-15 and b) 60 g tubes (NDC 61748-206-60, Marketed by Versapharm Inc., An Akorn Company, Lake Forest, IL, Manufactured by Hi-Tech, Pharmacal Co, Inc., Amityville, NY

Akorn Inc

Failed Stability Specifications; out-of specification value for homogeneity / phase separation.

November 14, 2016 · DrugView details →
Class ITerminated

Ultimate Body Tox PRO capsules, Proprietary Blend, 350 mg, 45 count bottle, Manufactured for: JSN Health, 305 Broadway, 7th Floor, New York, NY 10007.

Ultimate Body Tox

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.

November 13, 2016 · DrugView details →
Class IITerminated

L-Cysteine Hydrochloride Injection, USP, 50 mg/mL, 50 mL Pharmacy Bulk Package Vials (NDC 66758-005-01), packaged in 5 x 50 mL Vials per carton(NDC 66758-005-02), Rx only, Manufactured for: Sandoz, Inc., Princeton, NJ.

Sandoz Inc

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.

November 9, 2016 · DrugView details →
Class IITerminated

Lactulose Solution, USP, 10 g/15 mL, 15 mL unit dose cups (NDC 66689-039-01), packaged in 15 mL x 50 unit dose cups per case (NDC 66689-039-50), Rx only, Manufactured by VistaPharm, Inc., Largo, FL 33771.

VistaPharm, Inc.

Microbial Contamination of Non-Sterile Products: bulk solution tested positive for the presence of the bacteria, Burkholderia cepacia.

November 9, 2016 · DrugView details →
Class IITerminated

L-Cysteine Hydrochloride Injection, USP, 0.5 g/10 mL (50 mg/mL), 10 mL Single Dose Vial (NDC 66758-004-01), packaged in 10 x 10mL Vials per carton (NDC 66758-004-02), Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540.

Sandoz Inc

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.

November 9, 2016 · DrugView details →
Class IIITerminated

Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles (NDC 46706-201-06), OTC, Care-Tech Laboratories, Inc., St. Louis, MO 63139

Care-Tech Laboratories, Inc.

Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes, as well as defective or cracked caps.

November 8, 2016 · DrugView details →
Class IITerminated

LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620, NDC 60793-860-01

Pfizer Inc.

Superpotent

November 7, 2016 · DrugView details →
Class IIITerminated

Amoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01

West-Ward Pharmaceuticals Corp.

Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.

November 4, 2016 · DrugView details →
Class IIITerminated

Diltiazem HCl Extended-release Capsules, USP 120 mg, 100-count bottle (NDC 0378-5220-01), 500-count bottle (NDC 0378-5220-05), Rx Only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV, 26505 USA

Mylan Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: OOS results for known compound.

November 3, 2016 · DrugView details →
Class IIITerminated

BuPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, Rx Only, a) 30 count bottles (NDC 68382-354-06) and b) 500 count bottles (NDC 68382-354-05), Manufactured by: Cadila Healthcare LTD. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534

Zydus Pharmaceuticals USA Inc

Failed Dissolution Specifications; 6 month time point

November 2, 2016 · DrugView details →
Class IITerminated

PAPA/PHEN/PROST (papverine/phentolamine/prostaglandin) 30 mg/4 mg/0.04 mg/mL Injection, 1 mL vials, Fallon Wellness Pharmacy LLC, 1057 Troy-Schenectady Rd, Latham, NY 12110.

Fallon Wellness Pharmacy, L.L.C.

Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.

November 2, 2016 · DrugView details →
Class IITerminated

PAPA/PHEN/PROST (papverine/phentolamine/prostaglandin) 18 mg/0.6 mg/0.006 mg/mL Injection, 1 mL vials, Fallon Wellness Pharmacy LLC, 1057 Troy-Schenectady Rd, Latham, NY 12110.

Fallon Wellness Pharmacy, L.L.C.

Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.

November 2, 2016 · DrugView details →
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