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Akorn, Inc. recalls Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pha

Recalled January 19, 2022 · FDA recall D-0368-2022 · Akorn

Hazard
Labeling: Missing Label · FDA Class III
Units
8184 bottles
Sold at
Nationwide USA

Description

Labeling: Missing Label

Product
Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 --- NDC 50383-961-34
Manufacturer(s)
Akorn, Inc.

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

Akorn, Inc. recalls Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pha | RecallWatchUSA