SUN PHARMACEUTICAL INDUSTRIES INC 2025-04-16 Health moderate FDA
Health · FDA · Recall #FDA-D-0312-2025
Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC… Recall
Issued April 16, 2025 · SUN PHARMACEUTICAL INDUSTRIES INC
In April 2025, SUN PHARMACEUTICAL INDUSTRIES INC recalled the Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC…, a moderate health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Cross Contamination
What you should do
- 1 Stop using Gabapentin Capsules, USP 400 mg, Rx Only, Packaged in a) 500-count bottles, NDC… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact SUN PHARMACEUTICAL INDUSTRIES 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
- SUN PHARMACEUTICAL INDUSTRIES INC
- Category
- Health
- Recall date
- April 16, 2025
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0312-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- SUN PHARMACEUTICAL INDUSTRIES INC has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.