Apollo Care, LLC: Drug Recall

Recall #D-0634-2023 · 05/02/2023

Class II: Risk

Recall Details

Recall Number: D-0634-2023
Classification: Class II
Product Type: Drug
Recalling Firm: Apollo Care, LLC
Status: Ongoing
Date Initiated: 05/02/2023
Location: Columbia, MO, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 790 syringes

Reason for Recall

Lack of Assurance of Sterility

Product Description

FentaNYL 50 mcg/mL (2,500mcg Total Dose), 50 mL Syringe, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-910-25

Distribution Pattern

Missouri only

Other Recalls by Apollo Care, LLC

Class II: Risk 04/15/2025

Lack of Assurance of Sterility
Class II: Risk 05/02/2023

Lack of Assurance of Sterility
Class II: Risk 05/02/2023

Lack of Assurance of Sterility
Class II: Risk 05/02/2023

Lack of Assurance of Sterility
Class II: Risk 05/02/2023

Lack of Assurance of Sterility

View all recalls by Apollo Care, LLC →

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.