VistaPharm LLC 2023-11-15 Health moderate FDA
Health · FDA · Recall #FDA-D-0093-2024
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured… Recall
Issued November 15, 2023 · VistaPharm LLC
In November 2023, VistaPharm LLC recalled the Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured…, a moderate health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
What you should do
- 1 Stop using Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact VistaPharm LLC 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
- VistaPharm LLC
- Category
- Health
- Recall date
- November 15, 2023
- Units affected
- Not reported
- Sold at
- Nationwide and Saudi Arabia
- Recall number
- FDA-D-0093-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- VistaPharm LLC has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.