Akorn recalls PrednisoLONE Oral Solution 15mg/5mL bottles due to incomplete induction seals that may cause contamination. Affected units have NDC 50383-042-24, Lot# 379804.
Defective Container: Product has incomplete induction seals.
Akorn is recalling PrednisoLONE Oral Solution bottles that have incomplete induction seals. This defect could allow contamination, so affected users should stop using the product immediately.
The container's induction seals are incomplete, which may allow contaminants to enter the solution. This could lead to contamination of the medication, potentially causing health issues if used.
Prescription users of PrednisoLONE Oral Solution 15 mg per 5 mL, 240 ml bottles. Those with the specific NDC and lot number are most at risk.
Check for the NDC code 50383-042-24 and lot number 379804 on the bottle. The product is a prescription-only oral solution sold by HI-TECH PHARMACAL CO., INC. in Amityville, NY.
Immediately stop using the recalled PrednisoLONE Oral Solution bottles with incomplete induction seals.
No, the product has incomplete induction seals that may cause contamination. Do not use it.
The NDC number is 50383-042-24.
Check for NDC 50383-042-24 and lot number 379804 on the bottle label.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-1361-2022 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-1361-2022 from Akorn. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
