D-0276-2023 Class II Terminated

Recalled by Sentara Infusion Services — Chesapeake, VA

FDA drug recall D-0276-2023 was initiated by Sentara Infusion Services on Dec 27, 2022 and is designated Class II. Reason for recall: Lack of sterility assurance The recall status is terminated (terminated Feb 20, 2026). Affected quantity: 20 bags.

Recall Details

Product Type
Drugs
Report Date
Feb 22, 2023
Initiation Date
Dec 27, 2022
Termination Date
Feb 20, 2026
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
20 bags

Product Description

Ampicillin/Sulbactam 3GM IN NS 100ML, antibiotic, Rx only, used with a home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,

Reason for Recall

Lack of sterility assurance

Distribution Pattern

Dispensed to Patients Nationwide.

Code Information

Beyond Use Date: December 25-December 30, 2022

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0276-2023
openFDA file date
Oct 21, 2026
Loaded by RegDataLab
Oct 23, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.