Sentara Infusion Services: Drug Recall

Recall #D-0322-2023 · 12/27/2022

Class II: Risk

Recall Details

Recall Number
D-0322-2023
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
155 bags

Reason for Recall

Lack of sterility assurance

Product Description

Vancomycin (a) 1.25GM IN NS 250ML, (b) 1.5GM IN NS 300ML, (c) 1000MG IN NS 200ML (d) 2GM IN 400ML NS, (e) 900MG IN NS 180ML, (f) 500 MG NS 100ML, (g) 750 MG NS 150ML, antibiotic, Rx only, use with home pump, 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

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.