FDAFDA · Food and drugs·Recall number D-1361-2022
PrednisoLONE Oral Solution USP, 15 mg per 5 mL, 240 ml bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC: 50383-042-24
Published August 24, 2022 · Recall initiated: August 1, 2022
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Defective Container: Product has incomplete induction seals.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Akorn, Inc
- Distributor
- Nationwide USA
- Lot
- Lot# 379804, Exp. 8/31/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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