Showing 7,541–7,560 of 17,964 drug recalls
Drug Recall
Terminated
Historical record Class II
fentaNYL 0.05MG/ML INJ SOL (PF), 55ML per syringe (C-II) RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0118-55 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
EPINEPHrine 4MG ADDED TO D5W 5%, 250 ML per bag, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0113-22 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
EPHEDRINE 5MG/ML (PF) SYRINGE, 5 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0201-85 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
Edetate Disodium150mg/mL PFV, 10 ML per Vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0934-11 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
EDETATE DISODIUM 15% INJECTABLE, 100 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0922-11 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
EDETATE DISODIUM 30% INJECTABLE, 100 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0931-11 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
diazePAM 5 MG/ML INJECTION SOLUTION (C-IV) SYR, 2 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0929-02 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
DEXTROSE 50% INJECTION SOLUTION (PF) VIAL, 50 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0969-89 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
DEXTROSE 50% INJECTION SOLUTION (PF) SYRINGE, 50 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0969-89 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
DEXPANTHENOL 250MG/ML (MDV) INJECTION SOLN, 30ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0932-30 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
CALCIUM GLUCONATE 5% INJECTION SOLUTION (MDV), 20 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0903-20 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
CALCIUM CHLORIDE 100MG/ML (PFV) INJ SOLN, 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0920-10 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
BUFFERED LIDOCAINE HCL 1% INJECTION SOL (PF) SYR, 0.5 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0139-84 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
BUFFERED LIDOCAINE HCL 1% INJECTION SOLUTION (PF), 10ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0139-10 by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
Avastin, 25MG/ML Syringe, [a) 0.1 mL NDC 70731-0197-91; b) 0.12 mL NDC 70731-0197-92; c) 0.15 mL NDC 70731-0197-93] per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. by RXQ Compounding LLC
Reason
Lack of Assurance of Sterility Recall initiated
June 19, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide USA
View recall →
Drug Recall
Terminated
Historical record Class II
DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL Antihistamine, Mixed berry Flavor, 20 Pre-measured Single-Use vials per Carton, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, UPC 370302255010 by Unipharma, Llc.
Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia. Recall initiated
July 15, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide in the US.
View recall →
Drug Recall
Terminated
Historical record Class II
CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 12.5 mg/5 mL Oral Solution, Antihistamine, Mixed Berry Flavor, 20 Single-Use Vials per Carton, 0.17 fl. oz. (5 mL) Each, 3.4 fl. oz. (100 mL) Total Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, NDC 69842-261-01 UPC 050428597156 by Unipharma, Llc.
Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia. Recall initiated
July 15, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide in the US.
View recall →
Drug Recall
Terminated
Historical record Class II
Fungo Off Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808 by Herbal Doctor Remedies
Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Recall initiated
July 12, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide within the United States and Brazil and on the internet
View recall →
Drug Recall
Terminated
Historical record Class II
Asma Stopper Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808 by Herbal Doctor Remedies
Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Recall initiated
July 12, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide within the United States and Brazil and on the internet
View recall →
Drug Recall
Terminated
Historical record Class II
Anemia Off, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808 by Herbal Doctor Remedies
Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Recall initiated
July 12, 2019 Reported by FDA
August 14, 2019 Distribution
Nationwide within the United States and Brazil and on the internet
View recall →
Data last updated: September 18, 2026 ET
This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace
does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice --
always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take.
Read the full medical disclaimer .
