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Akorn, Inc. recalls Granisetron HCl Injection, USP, 1 mg/mL, packaged in a) 1mL and b) 4 mL vials, Rx Only, For Intravenous Use Only, Manufa

Recalled June 7, 2023 · FDA recall D-0806-2023 · Akorn

Hazard
CGMP Deviations: Firm went out of business and could no longer continue stability studies. · FDA Class II
Units
N/A
Sold at
Nationwide in the USA and Puerto Rico

Description

CGMP Deviations: Firm went out of business and could no longer continue stability studies.

Product
Granisetron HCl Injection, USP, 1 mg/mL, packaged in a) 1mL and b) 4 mL vials, Rx Only, For Intravenous Use Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. ALL NDCs
Manufacturer(s)
Akorn, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Akorn, Inc. recalls Granisetron HCl Injection, USP, 1 mg/mL, packaged in a) 1mL and b) 4 mL vials, Rx Only, For Intravenous Use Only, Manufa | RecallWatchUSA