FDAJune 5, 2020drug

Prednisolone Sodium Phosphate Oral Solution, 5 mg/5 mL, 120 mL Bottle, Rx only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC: 50383-040-04

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Discoloration: Out of Specification (OOS) result for APHA Color Test.

What to do

FDA enforcement status: Terminated

Brands named

akorn

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →