Akorn, Inc 2022-08-24 Health serious FDA
Health · FDA · Recall #FDA-D-1361-2022
PrednisoLONE Oral Solution USP, 15 mg per 5 mL, 240 ml bottle, Rx Only, HI-TECH PHARMACAL… Recall
Issued August 24, 2022 · Akorn, Inc
In August 2022, Akorn, Inc recalled the PrednisoLONE Oral Solution USP, 15 mg per 5 mL, 240 ml bottle, Rx Only, HI-TECH PHARMACAL…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Defective Container: Product has incomplete induction seals.
What you should do
- 1 Stop using PrednisoLONE Oral Solution USP, 15 mg per 5 mL, 240 ml bottle, Rx Only, HI-TECH PHARMACAL… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Akorn, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Akorn, Inc
- Category
- Health
- Recall date
- August 24, 2022
- Units affected
- Not reported
- Sold at
- Nationwide USA
- Recall number
- FDA-D-1361-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Akorn, Inc has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.