FDAFDA · Food and drugs·Recall number D-0368-2022
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
Published January 19, 2022 · Recall initiated: December 3, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Missing Label
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Akorn, Inc.
- Distributor
- Nationwide USA
- Lot
- Lots: 377186 Exp. 2/28/2023; 377188 Exp. 3/31/2023
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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