SCA Pharmaceuticals, LLC: Drug Recall

Recall #D-0395-2024 · 11/09/2023

Class II: Risk

Recall Details

Recall Number
D-0395-2024
Classification
Class II
Product Type
Drug
Recalling Firm
SCA Pharmaceuticals, LLC
Status
Terminated
Date Initiated
11/09/2023
Location
Windsor, CT, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
548 bags

Reason for Recall

Lack of Assurance of Sterility

Product Description

fentaNYL 2,500 mcg/250 mL in 0.9% Sodium Chloride Injection (Concentration = 10 mcg/mL), 250 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, 877.550.5059, NDC 70004-0229-40 BAR code 70004022940

Distribution Pattern

Nationwide in the USA

Other Recalls by SCA Pharmaceuticals, LLC

View all recalls by SCA Pharmaceuticals, 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.