Sentara Infusion Services: Drug Recall

Recall #D-0324-2023 · 12/27/2022

Class II: Risk

Recall Details

Recall Number: D-0324-2023
Classification: Class II
Product Type: Drug
Recalling Firm: Sentara Infusion Services
Status: Completed
Date Initiated: 12/27/2022
Location: Chesapeake, VA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 1 bag

Reason for Recall

Lack of sterility assurance

Product Description

VITAMIN K(PHYTONADIONE) 2.5MG(0.25ML) SYRINGE, Rx only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,

Distribution Pattern

Dispensed to Patients Nationwide.

Other Recalls by Sentara Infusion Services

Class II: Risk 12/27/2022

Lack of sterility assurance
Class II: Risk 12/27/2022

Lack of sterility assurance
Class II: Risk 12/27/2022

Lack of sterility assurance
Class II: Risk 12/27/2022

Lack of sterility assurance
Class II: Risk 12/27/2022

Lack of sterility assurance

View all recalls by Sentara Infusion Services →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.